	title	geo_accession	status	submission_date	last_update_date	type	channel_count	source_name_ch1	organism_ch1	characteristics_ch1	characteristics_ch1.1	characteristics_ch1.2	characteristics_ch1.3	growth_protocol_ch1	molecule_ch1	extract_protocol_ch1	label_ch1	label_protocol_ch1	taxid_ch1	hyb_protocol	scan_protocol	description	description.1	data_processing	platform_id	contact_name	contact_email	contact_phone	contact_department	contact_institute	contact_address	contact_city	contact_zip/postal_code	contact_country	supplementary_file	data_row_count	cell type:ch1	disease status:ch1	tissue:ch1	treatment:ch1
GSM799722	MDD patient 3 before treatment	GSM799722	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 3 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D3A.CEL	MDD patient 3 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799722/suppl/GSM799722.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799723	MDD patient 4 before treatment	GSM799723	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 4 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D4A.CEL	MDD patient 4 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799723/suppl/GSM799723.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799724	MDD patient 1 before treatment	GSM799724	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 1 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D1A.CEL	MDD patient 1 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799724/suppl/GSM799724.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799725	MDD patient 2 before treatment	GSM799725	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 2 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D2A.CEL	MDD patient 2 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799725/suppl/GSM799725.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799726	MDD patient 5 before treatment	GSM799726	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 5 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D5A.CEL	MDD patient 5 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799726/suppl/GSM799726.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799727	health control 1	GSM799727	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 1	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C1.CEL	health control 1	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799727/suppl/GSM799727.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799728	health control 2	GSM799728	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 2	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C2.CEL	health control 2	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799728/suppl/GSM799728.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799729	health control 3	GSM799729	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 3	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C3.CEL	health control 3	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799729/suppl/GSM799729.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799730	health control 4	GSM799730	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 4	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C4.CEL	health control 4	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799730/suppl/GSM799730.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799731	health control 5	GSM799731	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 5	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C5.CEL	health control 5	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799731/suppl/GSM799731.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799732	health control 6	GSM799732	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 6	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C6.CEL	health control 6	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799732/suppl/GSM799732.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799733	health control 7	GSM799733	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 7	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C7.CEL	health control 7	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799733/suppl/GSM799733.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799734	health control 8	GSM799734	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	health control 8	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: healthy control		Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-C8.CEL	health control 8	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799734/suppl/GSM799734.CEL.gz	54675	lymphocytes	healthy control	peripheral blood	NA
GSM799735	SSD patient 10 before treatment	GSM799735	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 10 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D10A.CEL	MDD patient 10 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799735/suppl/GSM799735.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799736	SSD patient 11 before treatment	GSM799736	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 11 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D11A.CEL	MDD patient 11 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799736/suppl/GSM799736.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799737	SSD patient 11 after treatment with Venlafaxine	GSM799737	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 11 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D11B.CEL	MDD patient 11 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799737/suppl/GSM799737.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	after treatment with Venlafaxine
GSM799738	MDD patient 13 before treatment	GSM799738	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 13 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D13A.CEL	MDD patient 13 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799738/suppl/GSM799738.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799739	MDD patient 13 after treatment with Venlafaxine	GSM799739	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 13 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D13B.CEL	MDD patient 13 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799739/suppl/GSM799739.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799740	MDD patient 14 before treatment	GSM799740	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 14 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D14A.CEL	MDD patient 14 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799740/suppl/GSM799740.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799741	MDD patient 14 after treatment with Venlafaxine	GSM799741	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 14 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D14B.CEL	MDD patient 14 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799741/suppl/GSM799741.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799742	SSD patient 15 before treatment	GSM799742	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 15 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D15A.CEL	MDD patient 15 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799742/suppl/GSM799742.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799743	MDD patient 19 before treatment	GSM799743	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 19 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D19A.CEL	MDD patient 19 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799743/suppl/GSM799743.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	before treatment
GSM799744	MDD patient 19 after treatment with Venlafaxine	GSM799744	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 19 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D19B.CEL	MDD patient 19 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799744/suppl/GSM799744.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799745	MDD patient 1 after treatment with Venlafaxine	GSM799745	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 1 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D1B.CEL	MDD patient 1 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799745/suppl/GSM799745.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799746	SSD patient 21 before treatment	GSM799746	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 21 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D21A.CEL	MDD patient 21 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799746/suppl/GSM799746.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799747	SSD patient 21 after treatment with Venlafaxine	GSM799747	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 21 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D21B.CEL	MDD patient 21 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799747/suppl/GSM799747.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	after treatment with Venlafaxine
GSM799748	SSD patient 22 before treatment	GSM799748	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 22 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D22A.CEL	MDD patient 22 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799748/suppl/GSM799748.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799749	SSD patient 22 after treatment with Venlafaxine	GSM799749	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 22 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D22B.CEL	MDD patient 22 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799749/suppl/GSM799749.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	after treatment with Venlafaxine
GSM799750	SSD patient 24 before treatment	GSM799750	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 24 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D24A.CEL	MDD patient 24 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799750/suppl/GSM799750.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799751	SSD patient 29 after treatment with Venlafaxine	GSM799751	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 29 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D29-2.CEL	MDD patient 29 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799751/suppl/GSM799751.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	after treatment with Venlafaxine
GSM799752	SSD patient 29 before treatment	GSM799752	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 29 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D29A.CEL	MDD patient 29 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799752/suppl/GSM799752.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799753	MDD patient 2 after treatment with Venlafaxine	GSM799753	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 2 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D2B.CEL	MDD patient 2 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799753/suppl/GSM799753.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799754	SSD patient 30 before treatment	GSM799754	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 30 before treatment	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: before treatment	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D30-1.CEL	MDD patient 30 before treatment with venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799754/suppl/GSM799754.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	before treatment
GSM799755	SSD patient 30 after treatment with Venlafaxine	GSM799755	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	SSD patient 30 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: SSD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D30-2.CEL	MDD patient 30 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799755/suppl/GSM799755.CEL.gz	54675	lymphocytes	SSD patient	peripheral blood	after treatment with Venlafaxine
GSM799756	MDD patient 3 after treatment with Venlafaxine	GSM799756	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 3 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D3B.CEL	MDD patient 3 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799756/suppl/GSM799756.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799757	MDD patient 4 after treatment with Venlafaxine	GSM799757	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 4 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D4B.CEL	MDD patient 4 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799757/suppl/GSM799757.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
GSM799758	MDD patient 5 after treatment with Venlafaxine	GSM799758	Public on Mar 21 2012	Sep 21 2011	Mar 21 2012	RNA	1	MDD patient 5 after treatment with Venlafaxine	Homo sapiens	tissue: peripheral blood	cell type: lymphocytes	disease status: MDD patient	treatment: after treatment with Venlafaxine	Venous peripheral blood from fasting patients and healthy controls were collected during 7am to 9am.Peripheral blood lymphocytes were separated by Ficoll gradient centrifugation using Ficoll-PlaqueTM Plus (GE, Sweden) according to the manufacturer's protocol.	total RNA	Total RNA was extracted from lymphocytes using Trizol reagent (Invitrogen) according to the manufacturer's protocol. RNA concentrations were determined by Nanodrop ND-1000 (Nanodrop Technologies, Wilmington, DE). RNA quality was assessed on an Agilent 2100 Bioanalyzer	biotin	Total RNA were amplified, labeled and purified by using GeneChip 3’IVT Express Kit (Cat#901229, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions to obtain biotin labeled cRNA.	9606	Array hybridization and wash was performed using GeneChip® Hybridization, Wash and Stain Kit (Cat#900720, Affymetrix, Santa Clara, CA, US)in Hybridization Oven 645 (Cat#00-0331-220V, Affymetrix, Santa Clara, CA, US)and Fluidics Station 450 (Cat#00-0079, Affymetrix, Santa Clara, CA, US) followed the manufacturer’s instructions.	Slides were scanned by GeneChip® Scanner 3000 (Cat#00-00212, Affymetrix, Santa Clara, CA, US) and Command Console Software 3.1 (Affymetrix, Santa Clara, CA, US) with default settings.	CB2007224-D5B.CEL	MDD patient 5 after treatment with Venlafaxine	Raw data were normalized by RMA method, Gene Spring Software 11.0 (Agilent technologies, Santa Clara, CA, US). The values were log2 transformed.	GPL570	Zezhi,,Li	lizezhi1981@yahoo.cn	+86 13564648631	Division of Mood Disorders	 Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China 	600 South Wan Ping Road Shanghai 200030, China	Shanghai	200030	China	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM799nnn/GSM799758/suppl/GSM799758.CEL.gz	54675	lymphocytes	MDD patient	peripheral blood	after treatment with Venlafaxine
