Search results for the GEO ID: GSE9089 |
(Click on the check boxes provided under "Select for analysis", to initiate grouping) |
(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down) |
|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM230268 | GPL570 |
|
H1 embryonic stem cells - GFP (endothelial study)
|
H1 undifferentiated embryonic stem cells - GFP
|
derived from H1-GFP labeled
|
H1-ES
|
Sample_geo_accession | GSM230268
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230268/suppl/GSM230268_H1.CEL.gz
| Sample_relation | Reanalysis of: GSM225042
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230269 | GPL570 |
|
H1 embryoid bodies - GFP (endothelial study)
|
H1 day3.5 embryoid bodies - GFP
|
derived from H1-GFP labeled
|
H1-EB
|
Sample_geo_accession | GSM230269
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230269/suppl/GSM230269_EB.CEL.gz
| Sample_relation | Reanalysis of: GSM225043
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230270 | GPL570 |
|
H1 blast cells - GFP (endothelial study)
|
H1 blast cells - GFP
|
derived from H1-GFP labeled
|
H1-BL
|
Sample_geo_accession | GSM230270
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230270/suppl/GSM230270_BL.CEL.gz
| Sample_relation | Reanalysis of: GSM225044
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230271 | GPL570 |
|
H9 embryonic stem cells (endothelial study)
|
H9 undifferentiated embryonic stem cells
|
derived from H9
|
H9-ES
|
Sample_geo_accession | GSM230271
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230271/suppl/GSM230271_H9-ES.CEL.gz
| Sample_relation | Reanalysis of: GSM225045
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230272 | GPL570 |
|
H9 embryoid bodies (endothelial study)
|
H9 day3.5 embryoid bodies
|
derived from H10
|
H9-EB
|
Sample_geo_accession | GSM230272
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230272/suppl/GSM230272_H9-EBS.CEL.gz
| Sample_relation | Reanalysis of: GSM225046
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230273 | GPL570 |
|
H9 blast cells (endothelial study)
|
H9 blast cells
|
derived from H11
|
H9-BL
|
Sample_geo_accession | GSM230273
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_growth_protocol_ch1 | see supplementary information Lu et.al, Nature Methods, 2007 Jun;4(6):501-9.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by Qiagen RNAeasy kiit and was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, cRNA was hybridized for 16 hr.
| Sample_scan_protocol | Once the probe array has been hybridized, washed, and stained, it is scanned.
| Sample_data_processing | The data were analyzed with Robust Multi-Chip Analysis (RMA).
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230273/suppl/GSM230273_H9-BL.CEL.gz
| Sample_relation | Reanalysis of: GSM225047
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230274 | GPL570 |
|
CD31+ rep1 (endothelial study)
|
normal prostate
|
CD31+ MACS sorted cells
|
endothelial cells
|
Sample_geo_accession | GSM230274
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| 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 | Prostate tissue was MACS sorted for positive cells. Total RNA was extracted from the cell lysate using an RNeasy kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Approximately 200 ng of total RNA was processed to produce biotinylated cRNA targets.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures
| Sample_data_processing | RMA of .cel files with Genespring 7.2
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230274/suppl/GSM230274_CD31t_04-27-04.CEL.gz
| Sample_relation | Reanalysis of: GSM91313
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230275 | GPL570 |
|
CD31+ rep2 (endothelial study)
|
normal prostate
|
CD31+ MACS sorted cells
|
endothelial cells
|
Sample_geo_accession | GSM230275
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| 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 | Prostate tissue was MACS sorted for positive cells. Total RNA was extracted from the cell lysate using an RNeasy kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Approximately 200 ng of total RNA was processed to produce biotinylated cRNA targets.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures
| Sample_data_processing | RMA of .cel files with Genespring 7.2
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230275/suppl/GSM230275_20040701_04_CD31t_06-02-04.CEL.gz
| Sample_relation | Reanalysis of: GSM91320
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230276 | GPL570 |
|
CD31+ rep3 (endothelial study)
|
normal prostate
|
CD31+ MACS sorted cells
|
endothelial cells
|
Sample_geo_accession | GSM230276
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| 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 | Prostate tissue was MACS sorted for positive cells. Total RNA was extracted from the cell lysate using an RNeasy kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Approximately 200 ng of total RNA was processed to produce biotinylated cRNA targets.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures
| Sample_data_processing | RMA of .cel files with Genespring 7.2
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230276/suppl/GSM230276_20041215_10_CD31t_04-191_12-15-04.CEL.gz
| Sample_relation | Reanalysis of: GSM91321
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230277 | GPL570 |
|
CD31+ rep4 (endothelial study)
|
normal prostate
|
CD31+ MACS sorted cells
|
endothelial cells
|
Sample_geo_accession | GSM230277
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| 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 | Prostate tissue was MACS sorted for positive cells. Total RNA was extracted from the cell lysate using an RNeasy kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Approximately 200 ng of total RNA was processed to produce biotinylated cRNA targets.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures
| Sample_data_processing | RMA of .cel files with Genespring 7.2
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230277/suppl/GSM230277_20041215_11_CD31t_04-181_12-15-04.CEL.gz
| Sample_relation | Reanalysis of: GSM91322
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
|
GSM230278 | GPL570 |
|
CD31+ rep5 (endothelial study)
|
normal prostate
|
CD31+ MACS sorted cells
|
endothelial cells
|
Sample_geo_accession | GSM230278
| Sample_status | Public on Nov 01 2007
| Sample_submission_date | Sep 18 2007
| Sample_last_update_date | Aug 14 2011
| 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 | Prostate tissue was MACS sorted for positive cells. Total RNA was extracted from the cell lysate using an RNeasy kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Approximately 200 ng of total RNA was processed to produce biotinylated cRNA targets.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures
| Sample_data_processing | RMA of .cel files with Genespring 7.2
| Sample_platform_id | GPL570
| Sample_contact_name | Jennifer,A,Hipp
| Sample_contact_email | jenhipp@wfubmc.edu
| Sample_contact_laboratory | Atala
| Sample_contact_department | Institute for Regenerative Medicine
| Sample_contact_institute | Wake Forest School of Medicine
| Sample_contact_address | Medical Center Blvd
| Sample_contact_city | Winston-Salem
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27157
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM230nnn/GSM230278/suppl/GSM230278_20041215_12_CD31t_04-126_12-15-04.CEL.gz
| Sample_relation | Reanalysis of: GSM91323
| Sample_series_id | GSE9089
| Sample_series_id | GSE9196
| Sample_data_row_count | 54675
| |
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