Result

Search results for the GEO ID: GSE12034

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM304260

GPL570

human oocyte, biological rep1

Pool of 10 human oocytes

Genotype: Human Oocytes from reproductively healthy individuals with regular ovulatory cycles, male factor as the only cause for infertility Age: < 35 yrs.

Gene expression data from human oocyte.

Sample_geo_accession	GSM304260
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Aug 15 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Ovarian stimulation was performed under Gn-RH analog suppression [leuprolide acetate (Lupron); Abbott, Abbott Park, IL] in a daily s.c. dose of 0.5 mg. Recombinant FSH (rFSH, Gonal-f-Serono or Puregon; Organon, Roseland, NJ) was administered in daily doses that ranged between 200 and 300 units, starting the second day of the mense. Follicular growth and estradiol levels were monitored every 2 to 3 days until follicles had a mean diameter between 18 and 20 mm. Oocyte maturation was achieved by an injection of 10,000 units of hCG (Pregnyl; Organon). Oocytes were retrieved from the ovary by aspiration using guided transvaginal ultrasound 36 h after hCG administration.
Sample_growth_protocol_ch1	Three hours after retrieval, oocytes were denuded from surrounding corona and cumulus cells by a brief incubation (10-30 s) in 80 units/ml hyaluronidase solution (LifeGlobal, Guilford, CT) and subsequent pipetting to completely eliminate other cells. Oocytes were then observed at high magnification to confirm maturity (metaphase II stage) and to confirm the absence of other cells. Each oocyte was rinsed in sterile PBS and lysed in 100 ml of extraction buffer (XB, Arcturus, Mountain View, CA) in an RNase/DNase/Pyrogen-free 0.5-ml microcentrifuge tube. Each sample was incubated for 30 min at 42°C, centrifuged at 3,000 ´ g for 2 min, and stored in liquid nitrogen until use.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated following the guanidium thiocyanate method by using the PicoPure RNA isolation kit (Arcturus, Sunnyvale, CA) following the manufacturer's instructions. However, only 6.5 ?l of elution buffer (Arcturus) was used, and the elution was repeated at least three times by using the first eluate. All RNA samples within the purification column were treated with the RNase-Free DNase (Qiagen, Valencia, CA). Extracted RNA was stored at ?80°C until used as template for cDNA synthesis.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304260/suppl/GSM304260.CEL.gz
Sample_relation	Reanalyzed by: GSM871485
Sample_relation	Reanalyzed by: GSE49910
Sample_series_id	GSE12034
Sample_data_row_count	54675

GSM304261

GPL570

human oocyte, biological rep2

Pool of 10 human oocytes

Genotype: Human Oocytes from reproductively healthy individuals with regular ovulatory cycles, male factor as the only cause for infertility Age: < 35 yrs.

Gene expression data from human oocyte.

Sample_geo_accession	GSM304261
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Aug 15 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Ovarian stimulation was performed under Gn-RH analog suppression [leuprolide acetate (Lupron); Abbott, Abbott Park, IL] in a daily s.c. dose of 0.5 mg. Recombinant FSH (rFSH, Gonal-f-Serono or Puregon; Organon, Roseland, NJ) was administered in daily doses that ranged between 200 and 300 units, starting the second day of the mense. Follicular growth and estradiol levels were monitored every 2 to 3 days until follicles had a mean diameter between 18 and 20 mm. Oocyte maturation was achieved by an injection of 10,000 units of hCG (Pregnyl; Organon). Oocytes were retrieved from the ovary by aspiration using guided transvaginal ultrasound 36 h after hCG administration.
Sample_growth_protocol_ch1	Three hours after retrieval, oocytes were denuded from surrounding corona and cumulus cells by a brief incubation (10-30 s) in 80 units/ml hyaluronidase solution (LifeGlobal, Guilford, CT) and subsequent pipetting to completely eliminate other cells. Oocytes were then observed at high magnification to confirm maturity (metaphase II stage) and to confirm the absence of other cells. Each oocyte was rinsed in sterile PBS and lysed in 100 ml of extraction buffer (XB, Arcturus, Mountain View, CA) in an RNase/DNase/Pyrogen-free 0.5-ml microcentrifuge tube. Each sample was incubated for 30 min at 42°C, centrifuged at 3,000 ´ g for 2 min, and stored in liquid nitrogen until use.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated following the guanidium thiocyanate method by using the PicoPure RNA isolation kit (Arcturus, Sunnyvale, CA) following the manufacturer's instructions. However, only 6.5 ?l of elution buffer (Arcturus) was used, and the elution was repeated at least three times by using the first eluate. All RNA samples within the purification column were treated with the RNase-Free DNase (Qiagen, Valencia, CA). Extracted RNA was stored at ?80°C until used as template for cDNA synthesis.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304261/suppl/GSM304261.CEL.gz
Sample_relation	Reanalyzed by: GSM871486
Sample_relation	Reanalyzed by: GSE49910
Sample_series_id	GSE12034
Sample_data_row_count	54675

GSM304262

GPL570

human oocyte, biological rep3

Pool of 10 human oocytes

Genotype: Human Oocytes from reproductively healthy individuals with regular ovulatory cycles, male factor as the only cause for infertility Age: < 35 yrs.

Gene expression data from human oocyte.

Sample_geo_accession	GSM304262
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Aug 15 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Ovarian stimulation was performed under Gn-RH analog suppression [leuprolide acetate (Lupron); Abbott, Abbott Park, IL] in a daily s.c. dose of 0.5 mg. Recombinant FSH (rFSH, Gonal-f-Serono or Puregon; Organon, Roseland, NJ) was administered in daily doses that ranged between 200 and 300 units, starting the second day of the mense. Follicular growth and estradiol levels were monitored every 2 to 3 days until follicles had a mean diameter between 18 and 20 mm. Oocyte maturation was achieved by an injection of 10,000 units of hCG (Pregnyl; Organon). Oocytes were retrieved from the ovary by aspiration using guided transvaginal ultrasound 36 h after hCG administration.
Sample_growth_protocol_ch1	Three hours after retrieval, oocytes were denuded from surrounding corona and cumulus cells by a brief incubation (10-30 s) in 80 units/ml hyaluronidase solution (LifeGlobal, Guilford, CT) and subsequent pipetting to completely eliminate other cells. Oocytes were then observed at high magnification to confirm maturity (metaphase II stage) and to confirm the absence of other cells. Each oocyte was rinsed in sterile PBS and lysed in 100 ml of extraction buffer (XB, Arcturus, Mountain View, CA) in an RNase/DNase/Pyrogen-free 0.5-ml microcentrifuge tube. Each sample was incubated for 30 min at 42°C, centrifuged at 3,000 ´ g for 2 min, and stored in liquid nitrogen until use.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was isolated following the guanidium thiocyanate method by using the PicoPure RNA isolation kit (Arcturus, Sunnyvale, CA) following the manufacturer's instructions. However, only 6.5 ?l of elution buffer (Arcturus) was used, and the elution was repeated at least three times by using the first eluate. All RNA samples within the purification column were treated with the RNase-Free DNase (Qiagen, Valencia, CA). Extracted RNA was stored at ?80°C until used as template for cDNA synthesis.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304262/suppl/GSM304262.CEL.gz
Sample_relation	Reanalyzed by: GSM871487
Sample_relation	Reanalyzed by: GSE49910
Sample_series_id	GSE12034
Sample_data_row_count	54675

GSM304263

GPL570

human reference, biological rep1

Pool of ten normal human tissues for reference

Genotype: 10 different normal human tissues, including skeletal muscle, kidney, lung, colon, liver, spleen, breast, brain, heart, and stomach. Age: N/A

Gene expression data from pool of 10 normal human tissue.

Sample_geo_accession	GSM304263
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Jul 14 2008
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Samples are obtained from Ambion
Sample_growth_protocol_ch1	Samples are obtained from Ambion.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The samples are processed using Ambion's RNA isolation reagents to produce highly pure, intact RNA. A stringent DNase treatment is performed to ensure that the RNA is ready for use in any downstream application, including RT-PCR.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304263/suppl/GSM304263.CEL.gz
Sample_series_id	GSE12034
Sample_data_row_count	54675

GSM304264

GPL570

human reference, biological rep2

Pool of ten normal human tissues for reference

Genotype: 10 different normal human tissues, including skeletal muscle, kidney, lung, colon, liver, spleen, breast, brain, heart, and stomach. Age: N/A

Gene expression data from pool of 10 normal human tissue.

Sample_geo_accession	GSM304264
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Jul 14 2008
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Samples are obtained from Ambion
Sample_growth_protocol_ch1	Samples are obtained from Ambion.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The samples are processed using Ambion's RNA isolation reagents to produce highly pure, intact RNA. A stringent DNase treatment is performed to ensure that the RNA is ready for use in any downstream application, including RT-PCR.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304264/suppl/GSM304264.CEL.gz
Sample_series_id	GSE12034
Sample_data_row_count	54675

GSM304265

GPL570

human reference, biological rep3

Pool of ten normal human tissues for reference

Genotype: 10 different normal human tissues, including skeletal muscle, kidney, lung, colon, liver, spleen, breast, brain, heart, and stomach. Age: N/A

Gene expression data from pool of 10 normal human tissue.

Sample_geo_accession	GSM304265
Sample_status	Public on Jul 09 2008
Sample_submission_date	Jul 08 2008
Sample_last_update_date	Jul 14 2008
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	Samples are obtained from Ambion
Sample_growth_protocol_ch1	Samples are obtained from Ambion.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The samples are processed using Ambion's RNA isolation reagents to produce highly pure, intact RNA. A stringent DNase treatment is performed to ensure that the RNA is ready for use in any downstream application, including RT-PCR.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Hybridization cocktails of 300 ml containing 15 mg of fragmented biotin-labeled aRNA and biotinylated exogenous hybridization controls (50 pM control Oligo B2, Eukaryotic hybridization controls) (BioB at 1.5 pM, BioC at 5 pM, BioD at 25 pM, and CreX at 100 pM), herring sperm DNA (0.1 mg/ml), BSA (0.5 mg/ml) in buffer (100 mM Mes/1M NaCl/20 mM EDTA/0.01% Tween 20) were hybridized to the GeneChip Human Genome U133 plus 2.0 array (Affymetrix, Santa Clara, CA). Hybridizations were performed automatically, and each array was prehybridized with all components except the fragmented biotin-labeled aRNA in a chamber at 45°C for 15 min with rotation at 60 rpm. The prehybridized array was then hybridized with the aRNA mixture for 16 h under the prehybridization conditions.
Sample_scan_protocol	The arrays were scanned using Affymetrix's high density GeneArray Scanner 3000 and imaged using Affymetrix GeneChip Operating Software (GCOS).
Sample_data_processing	The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
Sample_platform_id	GPL570
Sample_contact_name	Arif,Murat,Kocabas
Sample_contact_email	kocabas@msu.edu, hotu@bidmc.harvard.edu
Sample_contact_phone	517-432-8254
Sample_contact_fax	517-432-8742
Sample_contact_laboratory	Cellular Reprogramming Laboratory
Sample_contact_department	Animal Science
Sample_contact_institute	Michigan State University
Sample_contact_address	B270 Anthony Hall
Sample_contact_city	East Lansing
Sample_contact_state	MI
Sample_contact_zip/postal_code	48824
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM304nnn/GSM304265/suppl/GSM304265.CEL.gz
Sample_series_id	GSE12034
Sample_data_row_count	54675

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