Result

Search results for the GEO ID: GSE17353

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(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down)

GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM433796

GPL570

EPC2-hTERT_ Normoxia_ Exp1_rep1

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433796
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433796/suppl/GSM433796.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433797

GPL570

EPC2-hTERT_Normoxia_Exp1_rep2

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433797
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433797/suppl/GSM433797.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433798

GPL570

EPC2-hTERT_Hypoxia_Exp1_rep1

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433798
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433798/suppl/GSM433798.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433799

GPL570

EPC2-hTERT_Hypoxia_Exp1_rep2

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433799
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433799/suppl/GSM433799.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433800

GPL570

EPC2-hTERT_Normoxia_Exp2_rep1

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433800
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433800/suppl/GSM433800.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433801

GPL570

EPC2-hTERT_Normoxia_Exp2_rep2

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433801
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433801/suppl/GSM433801.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433802

GPL570

EPC2-hTERT_Hypoxia_Exp2_rep1

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433802
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433802/suppl/GSM433802.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

GSM433803

GPL570

EPC2-hTERT_Hypoxia_Exp2_rep2

esophageal epithelial cells (keratinocytes)

cells: epithelial cells (keratinocytes) genotype: hTERT-immortalized, non-transformed

none

Sample_geo_accession	GSM433803
Sample_status	Public on Sep 01 2009
Sample_submission_date	Jul 27 2009
Sample_last_update_date	Jul 27 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	EPC2-hTERT cells were exposed to either 21% O2 (normoxia) or 0.2% O2 (severe hypoxia) for 24 hrs. in experiment 1 (Exp 1) and either 21% O2 (normoxia) or 1% O2 (moderate hypoxia) for 24 hrs. in experiment 2 (Exp 2).
Sample_growth_protocol_ch1	EPC2-hTERT cells were grown under normoxic conditions (21% O2, 5% CO2, 95% humidity) at 37°C in serum free medium (Keratinocyte-SFM)(Invitrogen) supplemented with 1 ng/ml epidermal growth factor and 50 µg/ml bovine pituitary extract.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA) was used to extract total RNA according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
Sample_hyb_protocol	Hybridization of cRNAs to Affymetrix chips were performed according manufacturer's instructions
Sample_scan_protocol	Scanning of Affymetrix chips were performed according manufacturer's instructions
Sample_data_processing	.CEL files (probe level data) were exported from Affymetrix® GeneChip® Operating Software which was also used to calculate detection flags, which were exported in .chp files. Probe level data (.CEL files) were imported with Partek Genomics Suite (v. 6.4, Partek, Inc., St. Louis, MO). The data were normalized and summarized to the probe set level using GC-RMA, yielding log2 intensities for all probe sets on the array. These intensity values were then filtered based on the detection flags, retaining only those probe sets flagged as present in at least 1 of 4 samples for each of the hypoxia-exposed cell experiments
Sample_platform_id	GPL570
Sample_contact_name	Hiroshi,,Nakagawa
Sample_contact_email	nakagawh@mail.med.upenn.edu
Sample_contact_phone	215-573-1867
Sample_contact_fax	215-573-2024
Sample_contact_laboratory	Nakagawa
Sample_contact_department	Gastroenterology Division
Sample_contact_institute	University of Pennsylvania
Sample_contact_address	415 Curie Blvd.
Sample_contact_city	Philadelphia
Sample_contact_state	PA
Sample_contact_zip/postal_code	19104
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM433nnn/GSM433803/suppl/GSM433803.CEL.gz
Sample_series_id	GSE17353
Sample_data_row_count	35166

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