Search results for the GEO ID: GSE6257  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM143717 | GPL570 |
|
Human lymphatic endothelial cells Control_Rep 1
|
skin samples obtained healthy human donars during elective surgery at the Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143717
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 07 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer
| | Sample_treatment_protocol_ch1 | (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb , followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). cells cultured with/without TNFalpha treatment at 1 ng/ml.
| | Sample_growth_protocol_ch1 | cells cultured overnight in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridisations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143717/suppl/GSM143717.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
|
GSM143898 | GPL570 |
|
Human lymphatic endothelial cells Control_Rep 2
|
Skin samples obtained from healthy human donors during elective surgery at the Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143898
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 08 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb, followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). HDLEC were cultured for 48h in EGM2MV medium alone.
| | Sample_growth_protocol_ch1 | HDLEC were cultured overnight in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridizations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143898/suppl/GSM143898.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
|
GSM143900 | GPL570 |
|
Human lymphatic endothelial cells Control_Rep 3
|
Skin samples obtained from healthy human donors during elective surgery at the Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143900
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 08 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb, followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). HDLEC were cultured for 48h in EGM2MV medium alone.
| | Sample_growth_protocol_ch1 | HDLEC were cultured overnight in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridizations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143900/suppl/GSM143900.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
|
GSM143907 | GPL570 |
|
Human lymphatic endothelial cells TNFalpha_Rep 1
|
Primary lymphatic endothelial cells cultured in vitro for 72h +/- TNFalpha derived from skin samples obtained from healthy human donors during elective surgery.
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143907
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 08 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb, followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). HDLEC were cultured for 48h in EGM2MV medium supplemented with TNFalpha, 1 ng/ml.
| | Sample_growth_protocol_ch1 | HDLEC were cultured overnight in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridizations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143907/suppl/GSM143907.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
|
GSM143910 | GPL570 |
|
Human lymphatic endothelial cells TNFalpha_Rep 2
|
Primary lymphatic endothelial cells, cultured in vitro with TNFalpha, derived from skin samples obtained from healthy human donors during elective surgery.
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143910
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 08 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb, followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). HDLEC were cultured for 48h in EGM2MV medium supplemented with TNFalpha, 1 ng/ml.
| | Sample_growth_protocol_ch1 | HDLEC were cultured in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) supplemened with 1ng/ml TNFalpha at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridizations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143910/suppl/GSM143910.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
|
GSM143914 | GPL570 |
|
Human lymphatic endothelial cells TNFalpha_Rep 3
|
Primary lymphatic endothelial cells, cultured in vitro with TNFalpha, derived from skin samples obtained from healthy human donors during elective surgery.
|
Human dermal microvascular lymphatic endothelial cells (HDLEC) were prepared from healthy female adults undergoing elective surgery (breast reduction and abdominoplasty).
|
Here we have addressed important question of inflammation-induced mechanism for leukocyte transmigration of lymphatic vessel endothelium by comparing global gene expression profile of normal dermal lymphatic endothelial cells with/without TNFa added to the culture.
|
| Sample_geo_accession | GSM143914
| | Sample_status | Public on Dec 05 2006
| | Sample_submission_date | Nov 08 2006
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_biomaterial_provider_ch1 | Human samples obtained from Radcliffe Infirmary Hospital_Oxford (with full ethical approval)
| | Sample_treatment_protocol_ch1 | Human skin biopsy was digested overnight (4ºC) with Dispase®, 2 mg/ml (Gibco) in PBS, pH 7.5, to remove the epidermis. Cells were released from human tissue by scraping, passed through a 70μm cell strainer (BD Falcon) and expanded in 0.1% gelatine-coated flasks in complete EGM-2 MV medium. HDLEC were lifted with Accutase (PAALaboratories) then immuno-selected with mouse anti-human LYVE-1 mAb, followed by magnetic retrieval with appropriate MACS bead preparations (Miltenyi Biotech). HDLEC were cultured for 48h in EGM2MV medium supplemented with TNFalpha, 1 ng/ml.
| | Sample_growth_protocol_ch1 | HDLEC were cultured in complete EGM-2 MV medium(Cambrex Bio Science Walkersville Inc.) supplemened with 1ng/ml TNFalpha at 37ºC, 5 % CO2 in a humidified atmosphere, using plastic tissue culture flasks that had been pre-coated with gelatin (0.1%, Gibco)
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA extracted using Qiagen RNeasy.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | 8 microgram total RNA used in Affymetrix one cycle target labeling kit cat. no. 900493.
| | Sample_hyb_protocol | Fragmented labeled cRNA (15µg) was used in 300µl hybridization cocktail containing spiked controls (Affymetrix #900299). A 200µl of this hybridization cocktail was used on the chip and incubated at 45°C for 16 h in the hybridization oven, rotating at 60 rpm. Following hybridization, the arrays were processed using a Genechip Fluidics Station 400 according to recommended protocols (EukGE-WS2v5, Affymetrix) of double-staining and post-hybridizations washes.
| | Sample_scan_protocol | Fluorescent images were captured using gene Array Scanner 3000 and GCOS1.2 software (Affymetrix).
| | Sample_data_processing | We have used the genechip robust multi-array average expression measurements (GC-RMA) as implemented in BioConductor R statistics (www.bioconductor.org). Cell Intensity files (CEL) were used to obtain expression values for all the 54,675 probe sets (transcripts) on each array.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Dilair,,Baban
| | Sample_contact_email | dilair.baban@well.ox.ac.uk
| | Sample_contact_phone | +44(0)1865287521
| | Sample_contact_fax | +44(0)1865287501
| | Sample_contact_laboratory | Genomics
| | Sample_contact_department | Wellcome Trust Centre Human Genetics
| | Sample_contact_institute | University of Oxford
| | Sample_contact_address | Roosevelt Drive
| | Sample_contact_city | Oxford
| | Sample_contact_zip/postal_code | OX3 7BN
| | Sample_contact_country | United Kingdom
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM143nnn/GSM143914/suppl/GSM143914.CEL.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE6257
| | Sample_data_row_count | 54675
| | |
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