Result

Search results for the GEO ID: GSE18326

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM457629

GPL1261

FoxO3null_2_1

FoxO3 null mutant

strain: FVB/N tissue: forebrain

A_F3 NS2 #1_Mouse430_2

Sample_geo_accession	GSM457629
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457629/suppl/GSM457629.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457630

GPL1261

FoxO3null_2_2

FoxO3 null mutant

strain: FVB/N tissue: forebrain

A_F3 NS2 #2_Mouse430_2

Sample_geo_accession	GSM457630
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457630/suppl/GSM457630.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457631

GPL1261

WildType_2_1

wild type

strain: FVB/N tissue: forebrain

A_WT NS2 #1_Mouse430_2

Sample_geo_accession	GSM457631
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457631/suppl/GSM457631.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457632

GPL1261

WildType_2_2

wild type

strain: FVB/N tissue: forebrain

A_WT NS2 #2_Mouse430_2

Sample_geo_accession	GSM457632
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457632/suppl/GSM457632.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457633

GPL1261

FoxO3null_1_1

FoxO3 null mutant

strain: FVB/N tissue: forebrain

B_NS2-Fox03null #1_Mouse430_2

Sample_geo_accession	GSM457633
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457633/suppl/GSM457633.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457634

GPL1261

FoxO3null_1_2

FoxO3 null mutant

strain: FVB/N tissue: forebrain

B_NS2-Fox03null #2_Mouse430_2

Sample_geo_accession	GSM457634
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457634/suppl/GSM457634.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457635

GPL1261

WildType_1_1

wild type

strain: FVB/N tissue: forebrain

B_NS2-WT #1_Mouse430_2

Sample_geo_accession	GSM457635
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457635/suppl/GSM457635.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

GSM457636

GPL1261

WildType_1_2

wild type

strain: FVB/N tissue: forebrain

B_NS2-WT #2_Mouse430_2

Sample_geo_accession	GSM457636
Sample_status	Public on Nov 29 2009
Sample_submission_date	Sep 29 2009
Sample_last_update_date	Sep 29 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	NSC from neurospheres were enzymatically dissociated for 5-10 minutes at 37ºC with Accutase (Chemicon), then mechanically dissociated and seeded at a density of 5x104 cells/ml.
Sample_growth_protocol_ch1	Mouse forebrains were finely minced, digested for 30 minutes at 37ºC in HBSS media containing 2.5 U/ml Papain (Worthington), 1U/ml Dispase (Roche or Stem Cell Technologies), and 250 U/ml DNase I (Sigma) and mechanically dissociated. NSC/progenitors were purified using two successive Percoll gradients (25% then 65%) (Amersham) and plated on uncoated tissue culture dishes at a density of 105 cells/cm2 in NeuroBasal-A medium supplemented with penicillin (100 U/ml)-streptomycin (100 mg/ml)-glutamine (292 µg/ml), serum-free B27 supplement without vitamin A (2%), bFGF (20 ng/ml), and EGF (20 ng/ml) (self-renewal/proliferation media). Cells were incubated at 37ºC. Secondary neurospheres were collected 6 days after initial plating at 50000 cells/ml.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using the mirVana isolation kit following the manufacturer’s protocol (Ambion)
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin
Sample_hyb_protocol	Microarray hybridization was performed at the Stanford PAN facility. RNA was reverse-transcribed to cDNA followed by in vitro transcription and biotinylation. Biotinylated cRNAs were then fragmented, mixed with control cRNA fragments, and hybridized to Affymetrix oligonucleotide arrays (Mouse Genome 430 2.0 Array).
Sample_scan_protocol	Microarray scanning was performed at the Stanford PAN facility.
Sample_data_processing	Microarray results were pre-processed by performing a background adjustment and normalization with RMA (robust multi-array analysis) using Bioconductor.
Sample_platform_id	GPL1261
Sample_contact_name	Alex,,Morgan
Sample_contact_laboratory	Atul Butte Lab
Sample_contact_department	Biomedical Informatics
Sample_contact_institute	Stanford Medical School
Sample_contact_address	251 Campus Drive, MSOB X-215
Sample_contact_city	Stanford
Sample_contact_state	CA
Sample_contact_zip/postal_code	94305-5479
Sample_contact_country	USA
Sample_contact_web_link	http://www.stanford.edu/~alexmo/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM457nnn/GSM457636/suppl/GSM457636.CEL.gz
Sample_series_id	GSE18326
Sample_data_row_count	45101

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