Search results for the GEO ID: GSE11218 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM282712 | GPL1355 |
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A2B5+ biological replicate 1
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A2B5+ oligodendrocytes
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Fluorescent activated cell sorted A2B5+ oligodendrocytes isolated from post-natal day 7 rat whole brain
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Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
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Sample_geo_accession | GSM282712
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282712/suppl/GSM282712.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
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GSM282713 | GPL1355 |
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A2B5+ biological replicate-2
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A2B5+ oligodendrocytes
|
Fluorescent activated cell sorted A2B5+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282713
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282713/suppl/GSM282713.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
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GSM282714 | GPL1355 |
|
A2B5+ biological replicate 3
|
A2B5+ oligodendrocytes
|
Fluorescent activated cell sorted A2B5+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282714
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282714/suppl/GSM282714.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
|
GSM282715 | GPL1355 |
|
A2B5+ biological replicate 4
|
A2B5+ oligodendrocytes
|
Fluorescent activated cell sorted A2B5+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282715
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282715/suppl/GSM282715.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
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GSM282716 | GPL1355 |
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GalC+ biological replicate 1
|
GalC+ oligodendrocytes
|
Fluorescent activated cell sorted GalC+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282716
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNAeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282716/suppl/GSM282716.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
|
GSM282717 | GPL1355 |
|
GalC+ biological replicate 2
|
GalC+ oligodendrocytes
|
Fluorescent activated cell sorted GalC+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282717
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNAeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282717/suppl/GSM282717.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
|
GSM282718 | GPL1355 |
|
GalC+ biological replicate 3
|
GalC+ oligodendrocytes
|
Fluorescent activated cell sorted GalC+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282718
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNAeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282718/suppl/GSM282718.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
| |
|
GSM282719 | GPL1355 |
|
GalC+ biological replicate 4
|
GalC+ oligodendrocytes
|
Fluorescent activated cell sorted GalC+ oligodendrocytes isolated from post-natal day 7 rat whole brain
|
Oligodendrocytes were FAC sorted using cell surface expression of A2B5 and GALC to purifiy oligodendrocyte progenitors (A2B5+) and oligodendrocytes (GALC+) from postnatal day rat whole brains.
|
Sample_geo_accession | GSM282719
| Sample_status | Public on Jun 01 2008
| Sample_submission_date | Apr 20 2008
| Sample_last_update_date | Apr 21 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_biomaterial_provider_ch1 | Charles River
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNAeasy-Qiagen
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix small sample labeling protocol
| Sample_hyb_protocol | Affymetrix standard protocols were followed using the hybridization oven 640, and washing with the fluidics station 450
| Sample_scan_protocol | The microarrays were scanned with a genechip scanner 3000 7G
| Sample_data_processing | Cel files were imported into Genespring for preprocessing using RMA, and normalization using a global per-chip and per-gene normalization strategy
| Sample_platform_id | GPL1355
| Sample_contact_name | Joe,A,Nielsen
| Sample_contact_email | nielsenj@ninds.nih.gov
| Sample_contact_phone | 301-402-7350
| Sample_contact_laboratory | Section of Develpmental Genetics
| Sample_contact_institute | NIH/NINDS
| Sample_contact_address | 49 Convent Drive BD49,5A75
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-4479
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM282nnn/GSM282719/suppl/GSM282719.CEL.gz
| Sample_series_id | GSE11218
| Sample_data_row_count | 31099
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