Result

Search results for the GEO ID: GSE16447

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM413505

GPL570

IV_1

skin fibroblasts

tissue: skin cell type: fibroblasts gender: female

no further description

Sample_geo_accession	GSM413505
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413505/suppl/GSM413505.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413505/suppl/GSM413505.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413506

GPL570

IV_2

skin fibroblasts

tissue: skin cell type: fibroblasts gender: female

no further description

Sample_geo_accession	GSM413506
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413506/suppl/GSM413506.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413506/suppl/GSM413506.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413507

GPL570

IV_3

skin fibroblasts

tissue: skin cell type: fibroblasts gender: male

no further description

Sample_geo_accession	GSM413507
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413507/suppl/GSM413507.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413507/suppl/GSM413507.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413508

GPL570

IV_4

skin fibroblasts

tissue: skin cell type: fibroblasts gender: female

no further description

Sample_geo_accession	GSM413508
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413508/suppl/GSM413508.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413508/suppl/GSM413508.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413509

GPL570

IV_5

skin fibroblasts

tissue: skin cell type: fibroblasts gender: male

no further description

Sample_geo_accession	GSM413509
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413509/suppl/GSM413509.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413509/suppl/GSM413509.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413510

GPL570

IV_6

skin fibroblasts

tissue: skin cell type: fibroblasts gender: male

no further description

Sample_geo_accession	GSM413510
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413510/suppl/GSM413510.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413510/suppl/GSM413510.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413511

GPL570

IV-9

skin fibroblasts

tissue: skin cell type: fibroblasts gender: female

no further description

Sample_geo_accession	GSM413511
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413511/suppl/GSM413511.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413511/suppl/GSM413511.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413512

GPL570

Male Control

skin fibroblasts

tissue: skin cell type: fibroblasts gender: male

no further description

Sample_geo_accession	GSM413512
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413512/suppl/GSM413512.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413512/suppl/GSM413512.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

GSM413513

GPL570

Female Control

skin fibroblasts

tissue: skin cell type: fibroblasts gender: female

no further description

Sample_geo_accession	GSM413513
Sample_status	Public on Dec 11 2009
Sample_submission_date	Jun 05 2009
Sample_last_update_date	Dec 11 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted with Trizol reagent (GIBCO BRL Life Technologies, Gaithersburg, MD) and purified with Qiagen RNeasy mini columns (Qiagen, Valencia, CA) according to manufacturers’ protocols.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Briefly, 5 µg of total RNA was used to prepare double-stranded cDNA. Biotinylated cRNA was synthesized with an RNA transcript labeling kit and 20 µg of the cRNA product was chemically fragmented to approximately 50-200 nucleotides.
Sample_hyb_protocol	The fragmented cRNA was hybridized to an Affymetrix HG U133 Plus 2.0 chip. Chips were washed and stained using the EukGE-WS2v5 protocol on an Affymetrix fluidics 450 station. The stain included streptavidin-phycoerythrin (10 µg/mL) and biotinylated goat anti-streptavidin (3 µg/mL).
Sample_scan_protocol	Fluorescence intensities were captured with an argonion laser confocal scanner.
Sample_data_processing	Scanned output files were analyzed with GeneChip Operating Software 1.4 (GCOS; Affymetrix, Santa Clara, CA, USA). To examine the quality of the arrays the R function AffyQC was run on the CEL files.
Sample_data_processing	Data was normalized in R program using RMA (Robust Multichip Average) normalization. Data analysis was done using Omniviz software version 5.0.1 (Omniviz, Biowisdom USA Maynard, MA) software.
Sample_platform_id	GPL570
Sample_contact_name	J.,,Verkerk
Sample_contact_laboratory	Bioinformatics
Sample_contact_department	Bioinformatics
Sample_contact_institute	Erasmus Medical Center
Sample_contact_address	Molewaterplein 50
Sample_contact_city	Rotterdam
Sample_contact_zip/postal_code	3015GE
Sample_contact_country	Netherlands
Sample_contact_web_link	http://www.erasmusmc.nl/bioinformatica/?lang=en
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413513/suppl/GSM413513.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM413nnn/GSM413513/suppl/GSM413513.CHP.gz
Sample_series_id	GSE16447
Sample_data_row_count	54675

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