	title	geo_accession	status	submission_date	last_update_date	type	channel_count	source_name_ch1	organism_ch1	characteristics_ch1	characteristics_ch1.1	molecule_ch1	extract_protocol_ch1	extract_protocol_ch1.1	taxid_ch1	data_processing	data_processing.1	data_processing.2	data_processing.3	data_processing.4	data_processing.5	platform_id	contact_name	contact_email	contact_department	contact_institute	contact_address	contact_city	contact_state	contact_zip/postal_code	contact_country	data_row_count	instrument_model	library_selection	library_source	library_strategy	relation	relation.1	supplementary_file_1	disease state:ch1	tissue:ch1
GSM7461691	PeripheralBlood_Case01	GSM7461691	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652576	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607790	NONE	sALS	peripheral blood
GSM7461692	PeripheralBlood_Case02	GSM7461692	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652575	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607843	NONE	sALS	peripheral blood
GSM7461693	PeripheralBlood_Case03	GSM7461693	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652574	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607842	NONE	sALS	peripheral blood
GSM7461694	PeripheralBlood_Case04	GSM7461694	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652573	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607841	NONE	sALS	peripheral blood
GSM7461695	PeripheralBlood_Case05	GSM7461695	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652572	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607792	NONE	sALS	peripheral blood
GSM7461696	PeripheralBlood_Case06	GSM7461696	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652571	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607791	NONE	sALS	peripheral blood
GSM7461697	PeripheralBlood_Case07	GSM7461697	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652570	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607850	NONE	sALS	peripheral blood
GSM7461698	PeripheralBlood_Case08	GSM7461698	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652569	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607849	NONE	sALS	peripheral blood
GSM7461699	PeripheralBlood_Case09	GSM7461699	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652568	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607848	NONE	sALS	peripheral blood
GSM7461700	PeripheralBlood_Case10	GSM7461700	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652567	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607847	NONE	sALS	peripheral blood
GSM7461701	PeripheralBlood_Case11	GSM7461701	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652566	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607846	NONE	sALS	peripheral blood
GSM7461702	PeripheralBlood_Case12	GSM7461702	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652565	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607845	NONE	sALS	peripheral blood
GSM7461703	PeripheralBlood_Case13	GSM7461703	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652564	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607844	NONE	sALS	peripheral blood
GSM7461704	PeripheralBlood_Case14	GSM7461704	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652563	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607851	NONE	sALS	peripheral blood
GSM7461705	PeripheralBlood_Case15	GSM7461705	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652562	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607852	NONE	sALS	peripheral blood
GSM7461706	PeripheralBlood_Case16	GSM7461706	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652561	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607853	NONE	sALS	peripheral blood
GSM7461707	PeripheralBlood_Case17	GSM7461707	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652560	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607854	NONE	sALS	peripheral blood
GSM7461708	PeripheralBlood_Case18	GSM7461708	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652559	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607855	NONE	sALS	peripheral blood
GSM7461709	PeripheralBlood_Case19	GSM7461709	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652558	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607856	NONE	sALS	peripheral blood
GSM7461710	PeripheralBlood_Case20	GSM7461710	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652557	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607857	NONE	sALS	peripheral blood
GSM7461711	PeripheralBlood_Case21	GSM7461711	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652556	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607858	NONE	sALS	peripheral blood
GSM7461712	PeripheralBlood_Case22	GSM7461712	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652555	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607859	NONE	sALS	peripheral blood
GSM7461713	PeripheralBlood_Case23	GSM7461713	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652554	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607860	NONE	sALS	peripheral blood
GSM7461714	PeripheralBlood_Case24	GSM7461714	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652553	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607861	NONE	sALS	peripheral blood
GSM7461715	PeripheralBlood_Case25	GSM7461715	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652552	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607862	NONE	sALS	peripheral blood
GSM7461716	PeripheralBlood_Case26	GSM7461716	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652551	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607863	NONE	sALS	peripheral blood
GSM7461717	PeripheralBlood_Case27	GSM7461717	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652550	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607864	NONE	sALS	peripheral blood
GSM7461718	PeripheralBlood_Case28	GSM7461718	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652549	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607793	NONE	sALS	peripheral blood
GSM7461719	PeripheralBlood_Case29	GSM7461719	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652548	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607794	NONE	sALS	peripheral blood
GSM7461720	PeripheralBlood_Case30	GSM7461720	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652547	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607795	NONE	sALS	peripheral blood
GSM7461721	PeripheralBlood_Case31	GSM7461721	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652546	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607796	NONE	sALS	peripheral blood
GSM7461722	PeripheralBlood_Case32	GSM7461722	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652545	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607797	NONE	sALS	peripheral blood
GSM7461723	PeripheralBlood_Case33	GSM7461723	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652544	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607798	NONE	sALS	peripheral blood
GSM7461724	PeripheralBlood_Case34	GSM7461724	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652543	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607799	NONE	sALS	peripheral blood
GSM7461725	PeripheralBlood_Case35	GSM7461725	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652542	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607800	NONE	sALS	peripheral blood
GSM7461726	PeripheralBlood_Case36	GSM7461726	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652541	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607801	NONE	sALS	peripheral blood
GSM7461727	PeripheralBlood_Case37	GSM7461727	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652540	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607802	NONE	sALS	peripheral blood
GSM7461728	PeripheralBlood_Case38	GSM7461728	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652539	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607803	NONE	sALS	peripheral blood
GSM7461729	PeripheralBlood_Case39	GSM7461729	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652538	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607804	NONE	sALS	peripheral blood
GSM7461730	PeripheralBlood_Case40	GSM7461730	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652537	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607805	NONE	sALS	peripheral blood
GSM7461731	PeripheralBlood_Case41	GSM7461731	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652536	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607814	NONE	sALS	peripheral blood
GSM7461732	PeripheralBlood_Case42	GSM7461732	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652535	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607815	NONE	sALS	peripheral blood
GSM7461733	PeripheralBlood_Case43	GSM7461733	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652534	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607806	NONE	sALS	peripheral blood
GSM7461734	PeripheralBlood_Case44	GSM7461734	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652533	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607807	NONE	sALS	peripheral blood
GSM7461735	PeripheralBlood_Case45	GSM7461735	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652532	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607808	NONE	sALS	peripheral blood
GSM7461736	PeripheralBlood_Case46	GSM7461736	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652531	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607809	NONE	sALS	peripheral blood
GSM7461737	PeripheralBlood_Case47	GSM7461737	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652530	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607810	NONE	sALS	peripheral blood
GSM7461738	PeripheralBlood_Case48	GSM7461738	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652529	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607811	NONE	sALS	peripheral blood
GSM7461739	PeripheralBlood_Case49	GSM7461739	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652528	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607812	NONE	sALS	peripheral blood
GSM7461740	PeripheralBlood_Case50	GSM7461740	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652527	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607813	NONE	sALS	peripheral blood
GSM7461741	PeripheralBlood_Case51	GSM7461741	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652526	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607893	NONE	sALS	peripheral blood
GSM7461742	PeripheralBlood_Case52	GSM7461742	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652525	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607894	NONE	sALS	peripheral blood
GSM7461743	PeripheralBlood_Case53	GSM7461743	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652524	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607896	NONE	sALS	peripheral blood
GSM7461744	PeripheralBlood_Case54	GSM7461744	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652523	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607816	NONE	sALS	peripheral blood
GSM7461745	PeripheralBlood_Case55	GSM7461745	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652522	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607886	NONE	sALS	peripheral blood
GSM7461746	PeripheralBlood_Case56	GSM7461746	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652521	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607887	NONE	sALS	peripheral blood
GSM7461747	PeripheralBlood_Case57	GSM7461747	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652520	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607888	NONE	sALS	peripheral blood
GSM7461748	PeripheralBlood_Case58	GSM7461748	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652519	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607889	NONE	sALS	peripheral blood
GSM7461749	PeripheralBlood_Case59	GSM7461749	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652518	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607890	NONE	sALS	peripheral blood
GSM7461750	PeripheralBlood_Case60	GSM7461750	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652517	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607891	NONE	sALS	peripheral blood
GSM7461751	PeripheralBlood_Case61	GSM7461751	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652516	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607892	NONE	sALS	peripheral blood
GSM7461752	PeripheralBlood_Case62	GSM7461752	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652515	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607895	NONE	sALS	peripheral blood
GSM7461753	PeripheralBlood_Case63	GSM7461753	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652514	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607908	NONE	sALS	peripheral blood
GSM7461754	PeripheralBlood_Case64	GSM7461754	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652513	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607897	NONE	sALS	peripheral blood
GSM7461755	PeripheralBlood_Case65	GSM7461755	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652512	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607898	NONE	sALS	peripheral blood
GSM7461756	PeripheralBlood_Case66	GSM7461756	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652511	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607899	NONE	sALS	peripheral blood
GSM7461757	PeripheralBlood_Case67	GSM7461757	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652510	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607900	NONE	sALS	peripheral blood
GSM7461758	PeripheralBlood_Case68	GSM7461758	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652509	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607901	NONE	sALS	peripheral blood
GSM7461759	PeripheralBlood_Case69	GSM7461759	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652508	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607902	NONE	sALS	peripheral blood
GSM7461760	PeripheralBlood_Case70	GSM7461760	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652507	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607903	NONE	sALS	peripheral blood
GSM7461761	PeripheralBlood_Case71	GSM7461761	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652506	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607904	NONE	sALS	peripheral blood
GSM7461762	PeripheralBlood_Case72	GSM7461762	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652505	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607905	NONE	sALS	peripheral blood
GSM7461763	PeripheralBlood_Case73	GSM7461763	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652504	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607906	NONE	sALS	peripheral blood
GSM7461764	PeripheralBlood_Case74	GSM7461764	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652503	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607907	NONE	sALS	peripheral blood
GSM7461765	PeripheralBlood_Case75	GSM7461765	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652502	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607909	NONE	sALS	peripheral blood
GSM7461766	PeripheralBlood_Case76	GSM7461766	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652501	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607910	NONE	sALS	peripheral blood
GSM7461767	PeripheralBlood_Case77	GSM7461767	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652500	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607911	NONE	sALS	peripheral blood
GSM7461768	PeripheralBlood_Case78	GSM7461768	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652499	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607912	NONE	sALS	peripheral blood
GSM7461769	PeripheralBlood_Case79	GSM7461769	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652498	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607913	NONE	sALS	peripheral blood
GSM7461770	PeripheralBlood_Case80	GSM7461770	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652497	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607914	NONE	sALS	peripheral blood
GSM7461771	PeripheralBlood_Case81	GSM7461771	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652496	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607915	NONE	sALS	peripheral blood
GSM7461772	PeripheralBlood_Case82	GSM7461772	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652495	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607916	NONE	sALS	peripheral blood
GSM7461773	PeripheralBlood_Case83	GSM7461773	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652494	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607917	NONE	sALS	peripheral blood
GSM7461774	PeripheralBlood_Case84	GSM7461774	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652493	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607918	NONE	sALS	peripheral blood
GSM7461775	PeripheralBlood_Case85	GSM7461775	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652492	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607919	NONE	sALS	peripheral blood
GSM7461776	PeripheralBlood_Case86	GSM7461776	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652491	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607920	NONE	sALS	peripheral blood
GSM7461777	PeripheralBlood_Case87	GSM7461777	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652490	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607921	NONE	sALS	peripheral blood
GSM7461778	PeripheralBlood_Case88	GSM7461778	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652489	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607922	NONE	sALS	peripheral blood
GSM7461779	PeripheralBlood_Case89	GSM7461779	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652488	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607923	NONE	sALS	peripheral blood
GSM7461780	PeripheralBlood_Case90	GSM7461780	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652487	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607924	NONE	sALS	peripheral blood
GSM7461781	PeripheralBlood_Case91	GSM7461781	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652486	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607925	NONE	sALS	peripheral blood
GSM7461782	PeripheralBlood_Case92	GSM7461782	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652485	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607926	NONE	sALS	peripheral blood
GSM7461783	PeripheralBlood_Case93	GSM7461783	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652484	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607927	NONE	sALS	peripheral blood
GSM7461784	PeripheralBlood_Case94	GSM7461784	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652483	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607928	NONE	sALS	peripheral blood
GSM7461785	PeripheralBlood_Case95	GSM7461785	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652482	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607929	NONE	sALS	peripheral blood
GSM7461786	PeripheralBlood_Case96	GSM7461786	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: sALS	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652481	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607930	NONE	sALS	peripheral blood
GSM7461787	PeripheralBlood_Control01	GSM7461787	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652480	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607824	NONE	Healthy control	peripheral blood
GSM7461788	PeripheralBlood_Control02	GSM7461788	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652479	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607825	NONE	Healthy control	peripheral blood
GSM7461789	PeripheralBlood_Control03	GSM7461789	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652478	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607931	NONE	Healthy control	peripheral blood
GSM7461790	PeripheralBlood_Control04	GSM7461790	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652477	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607932	NONE	Healthy control	peripheral blood
GSM7461791	PeripheralBlood_Control05	GSM7461791	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652476	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607933	NONE	Healthy control	peripheral blood
GSM7461792	PeripheralBlood_Control06	GSM7461792	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652475	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607817	NONE	Healthy control	peripheral blood
GSM7461793	PeripheralBlood_Control07	GSM7461793	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652474	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607818	NONE	Healthy control	peripheral blood
GSM7461794	PeripheralBlood_Control08	GSM7461794	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652473	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607819	NONE	Healthy control	peripheral blood
GSM7461795	PeripheralBlood_Control09	GSM7461795	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652472	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607820	NONE	Healthy control	peripheral blood
GSM7461796	PeripheralBlood_Control10	GSM7461796	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652471	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607821	NONE	Healthy control	peripheral blood
GSM7461797	PeripheralBlood_Control11	GSM7461797	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652470	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607822	NONE	Healthy control	peripheral blood
GSM7461798	PeripheralBlood_Control12	GSM7461798	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652469	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607823	NONE	Healthy control	peripheral blood
GSM7461799	PeripheralBlood_Control13	GSM7461799	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652468	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607837	NONE	Healthy control	peripheral blood
GSM7461800	PeripheralBlood_Control14	GSM7461800	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652467	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607826	NONE	Healthy control	peripheral blood
GSM7461801	PeripheralBlood_Control15	GSM7461801	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652466	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607827	NONE	Healthy control	peripheral blood
GSM7461802	PeripheralBlood_Control16	GSM7461802	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652465	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607828	NONE	Healthy control	peripheral blood
GSM7461803	PeripheralBlood_Control17	GSM7461803	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652464	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607829	NONE	Healthy control	peripheral blood
GSM7461804	PeripheralBlood_Control18	GSM7461804	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652463	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607830	NONE	Healthy control	peripheral blood
GSM7461805	PeripheralBlood_Control19	GSM7461805	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652462	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607831	NONE	Healthy control	peripheral blood
GSM7461806	PeripheralBlood_Control20	GSM7461806	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652461	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607832	NONE	Healthy control	peripheral blood
GSM7461807	PeripheralBlood_Control21	GSM7461807	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652460	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607833	NONE	Healthy control	peripheral blood
GSM7461808	PeripheralBlood_Control22	GSM7461808	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652459	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607834	NONE	Healthy control	peripheral blood
GSM7461809	PeripheralBlood_Control23	GSM7461809	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652458	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607835	NONE	Healthy control	peripheral blood
GSM7461810	PeripheralBlood_Control24	GSM7461810	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652457	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607836	NONE	Healthy control	peripheral blood
GSM7461811	PeripheralBlood_Control25	GSM7461811	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652456	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607838	NONE	Healthy control	peripheral blood
GSM7461812	PeripheralBlood_Control26	GSM7461812	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652455	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607839	NONE	Healthy control	peripheral blood
GSM7461813	PeripheralBlood_Control27	GSM7461813	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652454	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607840	NONE	Healthy control	peripheral blood
GSM7461814	PeripheralBlood_Control28	GSM7461814	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652453	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607865	NONE	Healthy control	peripheral blood
GSM7461815	PeripheralBlood_Control29	GSM7461815	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652452	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607866	NONE	Healthy control	peripheral blood
GSM7461816	PeripheralBlood_Control30	GSM7461816	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652451	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607867	NONE	Healthy control	peripheral blood
GSM7461817	PeripheralBlood_Control31	GSM7461817	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652450	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607868	NONE	Healthy control	peripheral blood
GSM7461818	PeripheralBlood_Control32	GSM7461818	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652449	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607869	NONE	Healthy control	peripheral blood
GSM7461819	PeripheralBlood_Control33	GSM7461819	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652448	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607870	NONE	Healthy control	peripheral blood
GSM7461820	PeripheralBlood_Control34	GSM7461820	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652447	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607871	NONE	Healthy control	peripheral blood
GSM7461821	PeripheralBlood_Control35	GSM7461821	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652446	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607880	NONE	Healthy control	peripheral blood
GSM7461822	PeripheralBlood_Control36	GSM7461822	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652445	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607881	NONE	Healthy control	peripheral blood
GSM7461823	PeripheralBlood_Control37	GSM7461823	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652444	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607872	NONE	Healthy control	peripheral blood
GSM7461824	PeripheralBlood_Control38	GSM7461824	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652443	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607873	NONE	Healthy control	peripheral blood
GSM7461825	PeripheralBlood_Control39	GSM7461825	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652442	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607874	NONE	Healthy control	peripheral blood
GSM7461826	PeripheralBlood_Control40	GSM7461826	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652441	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607875	NONE	Healthy control	peripheral blood
GSM7461827	PeripheralBlood_Control41	GSM7461827	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652440	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607876	NONE	Healthy control	peripheral blood
GSM7461828	PeripheralBlood_Control42	GSM7461828	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652439	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607877	NONE	Healthy control	peripheral blood
GSM7461829	PeripheralBlood_Control43	GSM7461829	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652438	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607878	NONE	Healthy control	peripheral blood
GSM7461830	PeripheralBlood_Control44	GSM7461830	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652437	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607879	NONE	Healthy control	peripheral blood
GSM7461831	PeripheralBlood_Control45	GSM7461831	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652436	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607884	NONE	Healthy control	peripheral blood
GSM7461832	PeripheralBlood_Control46	GSM7461832	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652435	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607885	NONE	Healthy control	peripheral blood
GSM7461833	PeripheralBlood_Control47	GSM7461833	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652434	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607882	NONE	Healthy control	peripheral blood
GSM7461834	PeripheralBlood_Control48	GSM7461834	Public on Oct 12 2023	Jun 06 2023	Oct 12 2023	SRA	1	peripheral blood	Homo sapiens	tissue: peripheral blood	disease state: Healthy control	total RNA	Total RNA was extracted from peripheral blood using the QIASymphony automated liquid handing robot and the PAXgene Blood RNA kit (Qiagen, Hilden, Germany) as per standard protocol.	RNA-seq libraries were prepared from total RNA using the TruSeq Stranded mRNA Sample Prep kit (Illumina, CA, USA).	9606	Trimmomatic v0.38 was applied to raw FASTQ files to remove low quality reads and adaptor sequences.	Salmon v1.9.0 was used to build a transcriptome index and to quantify transcripts (default selective alignment with --seqBias and --gcBias flags).	Tximport v1.26.1 was used to convert transcript abundance estimates to gene-level counts with corresponding offset matrix.	Assembly: GRCh38	Supplementary files format and content: tab delimited text file including raw gene counts	Supplementary files format and content: tab delimited text file including tximport-generated offset matrix	GPL11154	Kelly,,Williams	kelly.williams@mq.edu.au	Motor Neuron Disease Centre	Macquarie University	75 Talavera Road	Sydney	NSW	2109	Australia	0	Illumina HiSeq 2000	cDNA	transcriptomic	RNA-Seq	BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN35652433	SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX20607883	NONE	Healthy control	peripheral blood
