Result

Search results for the GEO ID: GSE15902

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM399126

GPL1261

Whole Blood Chemical Hypoxic 1_8804

Whole Blood

stress: chemical hypoxia

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM399126
Sample_status	Public on Apr 25 2010
Sample_submission_date	Apr 29 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	At the beginning of the experiment mice were divided into two groups, control (room condition) and chemical hypoxic (room condition). For conditioning, the chemical hypoxic group was supplemented with 200ng of CoCl2 per 100ml/day. Animal’s weight and food intake were monitored daily. Food and water were changed daily during the course of the experiment. Before and after the experiments the hematocrit was monitored by taking blood from the tail vein of control and hypoxic animals. After 15 days animals were euthanized using CO2 after whole blood extraction from V. Cava for further analysis.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM399nnn/GSM399126/suppl/GSM399126.CEL.gz
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM399127

GPL1261

Whole Blood Chemical Hypoxic 2_8806

Whole Blood

stress: chemical hypoxia

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM399127
Sample_status	Public on Apr 25 2010
Sample_submission_date	Apr 29 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	At the beginning of the experiment mice were divided into two groups, control (room condition) and chemical hypoxic (room condition). For conditioning, the chemical hypoxic group was supplemented with 200ng of CoCl2 per 100ml/day. Animal’s weight and food intake were monitored daily. Food and water were changed daily during the course of the experiment. Before and after the experiments the hematocrit was monitored by taking blood from the tail vein of control and hypoxic animals. After 15 days animals were euthanized using CO2 after whole blood extraction from V. Cava for further analysis.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM399nnn/GSM399127/suppl/GSM399127.CEL.gz
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM399128

GPL1261

Whole Blood Chemical Hypoxic 3_8807

Whole Blood

stress: chemical hypoxia

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM399128
Sample_status	Public on Apr 25 2010
Sample_submission_date	Apr 29 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	At the beginning of the experiment mice were divided into two groups, control (room condition) and chemical hypoxic (room condition). For conditioning, the chemical hypoxic group was supplemented with 200ng of CoCl2 per 100ml/day. Animal’s weight and food intake were monitored daily. Food and water were changed daily during the course of the experiment. Before and after the experiments the hematocrit was monitored by taking blood from the tail vein of control and hypoxic animals. After 15 days animals were euthanized using CO2 after whole blood extraction from V. Cava for further analysis.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM399nnn/GSM399128/suppl/GSM399128.CEL.gz
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM399129

GPL1261

Whole Blood Chemical Hypoxic 4_8808

Whole Blood

stress: chemical hypoxia

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM399129
Sample_status	Public on Apr 25 2010
Sample_submission_date	Apr 29 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	At the beginning of the experiment mice were divided into two groups, control (room condition) and chemical hypoxic (room condition). For conditioning, the chemical hypoxic group was supplemented with 200ng of CoCl2 per 100ml/day. Animal’s weight and food intake were monitored daily. Food and water were changed daily during the course of the experiment. Before and after the experiments the hematocrit was monitored by taking blood from the tail vein of control and hypoxic animals. After 15 days animals were euthanized using CO2 after whole blood extraction from V. Cava for further analysis.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM399nnn/GSM399129/suppl/GSM399129.CEL.gz
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM444068

GPL1261

Whole Blood chamber Control 1 (5525)

Whole Blood

stress: control

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM444068
Sample_status	Public on Apr 25 2010
Sample_submission_date	Aug 25 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM444nnn/GSM444068/suppl/GSM444068.CEL.gz
Sample_relation	Reanalysis of: GSM397842
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM444069

GPL1261

Whole Blood Chamber Control 2 (5526)

Whole Blood

stress: control

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM444069
Sample_status	Public on Apr 25 2010
Sample_submission_date	Aug 25 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM444nnn/GSM444069/suppl/GSM444069.CEL.gz
Sample_relation	Reanalysis of: GSM397843
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM444070

GPL1261

Whole Blood Chamber Control 3 (5527)

Whole Blood

stress: control

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM444070
Sample_status	Public on Apr 25 2010
Sample_submission_date	Aug 25 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM444nnn/GSM444070/suppl/GSM444070.CEL.gz
Sample_relation	Reanalysis of: GSM397844
Sample_series_id	GSE15902
Sample_data_row_count	45101

GSM444071

GPL1261

Whole Blood Chamber Control 4 (5529)

Whole Blood

stress: control

Whole Blood was drawn from V. Cava.

Sample_geo_accession	GSM444071
Sample_status	Public on Apr 25 2010
Sample_submission_date	Aug 25 2009
Sample_last_update_date	Nov 30 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated and purified from 100ul of whole blood with the Mouse Ribopure-Blood RNA Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
Sample_hyb_protocol	15 micrograms of labeled cRNA from whole blood was fragmented, and 10ug was hybridized to Affymetrix Mouse 430 2.0 Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Sample_scan_protocol	The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Sample_data_processing	Quality control parameters such as scaling factors used to normalize the chips, average background, and noise were also evaluated. In addition, raw intensities for each probe set were stored in electronic formats by the GeneChip operating system 1.1 (Affymetrix) for GC-RMA analysis in PARTEK software later on.
Sample_platform_id	GPL1261
Sample_contact_name	Gabriel,,Willmann
Sample_contact_email	Gabriel.Willmann@med.uni-tuebingen.de
Sample_contact_institute	University Eye Hospital and Centre for Ophthalmology Tübingen
Sample_contact_address	Schleichstrasse 12-16
Sample_contact_city	Tübingen
Sample_contact_zip/postal_code	72076
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM444nnn/GSM444071/suppl/GSM444071.CEL.gz
Sample_relation	Reanalysis of: GSM397845
Sample_series_id	GSE15902
Sample_data_row_count	45101

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