Result

Search results for the GEO ID: GSE41558

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM1019090

GPL1261

Heart_WT_1

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: wild type tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019090
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019090/suppl/GSM1019090_mtb_BO_7959_MA2_30712.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019091

GPL1261

Heart_WT_2

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: wild type tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019091
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019091/suppl/GSM1019091_mtb_BO_7959_MA2_30713.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019092

GPL1261

Heart_WT_3

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: wild type tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019092
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019092/suppl/GSM1019092_mtb_BO_7959_MA2_30714.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019093

GPL1261

Heart_WT_4

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: wild type tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019093
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019093/suppl/GSM1019093_mtb_BO_7959_MA2_30715.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019094

GPL1261

Heart_KO_1

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: SRC-2 knockout (KO) tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019094
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019094/suppl/GSM1019094_mtb_BO_7959_MA2_30709.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019095

GPL1261

Heart_KO_2

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: SRC-2 knockout (KO) tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019095
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019095/suppl/GSM1019095_mtb_BO_7959_MA2_30710.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019096

GPL1261

Heart_KO_3

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: SRC-2 knockout (KO) tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019096
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019096/suppl/GSM1019096_mtb_BO_7959_MA2_30711.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

GSM1019097

GPL1261

Heart_KO_4

heart tissue, ad lib feeding, 10-12 weeks old

gender: male strain: C57B/6Jx129Sv genotype/variation: SRC-2 knockout (KO) tissue: heart age: 10-12 weeks old

Sample_geo_accession	GSM1019097
Sample_status	Public on Oct 13 2012
Sample_submission_date	Oct 12 2012
Sample_last_update_date	Oct 13 2012
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	Frozen hearts isolated from WT and SRC-2 KO animals were homogenized in buffer RLT and subsequent RNA was isolated using the RNEasy kit according to the manufacturer’s protocol (Qiagen).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	250ng of RNA isolated from total heart (RNeasy kit, Qiagen) for each sample was labeled using the new standard Affymetrix linear amplification protocol using the 3' IVT Express Kit. This was reverse-transcribed and cRNA was produced and biotinylated via in vitro transcription.
Sample_hyb_protocol	A hybridization cocktail containing Affymetrix spike-in controls and 15 μg fragmented, labeled cRNA was loaded onto a GeneChip® Mouse 430 2.0 array. The array was hybridized for 16 hours at 45°C with rotation at 60 rpm then washed and stained with a strepavidin, R-phycoerythrin conjugate stain using the FS 450_0001 Fluidics protocol setting.
Sample_scan_protocol	Signal amplification was done using biotinylated antistreptavidin. The stained array was scanned on the Affymetrix GeneChip® Scanner 3000. The images were analyzed and quality control metrics recorded using Affymetrix Command Console v3.
Sample_data_processing	We used the following software packages for data QC, statistical analysis and presentation of the results: Affymetrix Expression Console (www.affymetrix.com), Partek (www.partek.com), BRB Array Tools (linus.nci.nih.gov/BRB-ArrayTools.html), and dChip (biosun1.harvard.edu/complab/dchip). Expressions were estimated using the RMA (Multi-Array Analysis) method [38] with Partek software.
Sample_data_processing = Differentially expressed genes were found using the RVM (Random Variance Model) t-test, which is designed for small sample size experiments [39]. We used BRB Array Tools software, developed by Dr. Richard Simon and the BRB-ArrayTools Development Team. All genes were included in the comparison. For the genes represented by more than one probeset, we used the most highly expressed probeset. The cutoffs for differentially expressed genes were False Discovery Rate (FDR)	0.05.
Sample_platform_id	GPL1261
Sample_contact_name	Erin,,Reineke
Sample_contact_institute	Baylor College of Medicine
Sample_contact_address	One Baylor PLaza
Sample_contact_city	Houston
Sample_contact_state	TX
Sample_contact_zip/postal_code	77030
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1019nnn/GSM1019097/suppl/GSM1019097_mtb_BO_7959_MA2_30828.CEL.gz
Sample_series_id	GSE41558
Sample_data_row_count	45101

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