Search results for the GEO ID: GSE9300 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM237013 | GPL85 |
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Ovary postnatal day 0 replicate 1
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0-day rat ovary
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ovaries dissected from 0-day old Sprague-Dawley rats and cleaned of ovarian bursa.
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Chip ID=phil_P0_U34A_102502. RNA from zero-day old rat ovaries.
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Sample_geo_accession | GSM237013
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P0 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237013/suppl/GSM237013.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
|
GSM237014 | GPL85 |
|
Ovary postnatal day 0 replicate 2
|
0-day rat ovary
|
ovaries dissected from 0-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
Chip ID=Phil-PO-RGu34A-072403. RNA from zero-day old rat ovaries.
|
Sample_geo_accession | GSM237014
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P0 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237014/suppl/GSM237014.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
|
GSM237015 | GPL85 |
|
Ovary postnatal day 4 replicate 1
|
P4-day rat ovary
|
ovaries dissected from P4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
Chip ID=phil_P4_U34A_102502. RNA from four-day old rat ovaries.
|
Sample_geo_accession | GSM237015
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P4 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237015/suppl/GSM237015.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
|
GSM237016 | GPL85 |
|
Ovary postnatal day 4 replicate 2
|
P4-day rat ovary
|
ovaries dissected from P4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
Chip ID=Phil-P4-RGu34A-072403. RNA from four-day old rat ovaries.
|
Sample_geo_accession | GSM237016
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P4 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237016/suppl/GSM237016.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
|
GSM237017 | GPL85 |
|
Cultured ovary postnatal day 0 replicate 1
|
0-day rat ovary cultured 7 days
|
ovaries dissected from 0-day old Sprague-Dawley rats and cleaned of ovarian bursa and cultured for 7 days
|
Chip ID=Phil-Cult.Ovary-RGu34A-082603. RNA from zero-day old rat ovaries cultured 7 days.
|
Sample_geo_accession | GSM237017
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P0 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols. Whole ovaries were cultured as previously described (Nilsson, Parrott et al. 2001) on floating filters (0.4 um Millicell-CM, Millipore, Bedford, MD) in 0.5 ml Dulbecco's Modified Eagle's Medium (DMEM)-Ham's F-12 medium (1:1, vol/vol) containing 0.1 % bovine serum albumin (BSA, Sigma, St. Louis, MO), 0.1% Albumax (Gibco BRL, Gaithersburg, MD), 27.5 ?g/ml transferrin, 200 ng/ml insulin (human recombinant, Sigma), and 0.05 mg/ml L-ascorbic acid (Sigma) in a 4-well culture plate (Nunc plate, Applied Scientific, South San Francisco, CA). Medium was supplemented with penicillin and streptomycin to prevent bacterial contamination.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237017/suppl/GSM237017.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
|
GSM237018 | GPL85 |
|
Cultured ovary postnatal day 0 replicate 2
|
0-day rat ovary cultured 7 days
|
ovaries dissected from 0-day old Sprague-Dawley rats and cleaned of ovarian bursaand cultured for 7 days
|
Chip ID=phil-cultured-U34A-022703. RNA from zero-day old rat ovaries cultured 7 days.
|
Sample_geo_accession | GSM237018
| Sample_status | Public on Oct 12 2007
| Sample_submission_date | Oct 11 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Female day P0 rat pups were euthanized and rat ovaries were removed according to IACUC-approved animal use protocols. Whole ovaries were cultured as previously described (Nilsson, Parrott et al. 2001) on floating filters (0.4 um Millicell-CM, Millipore, Bedford, MD) in 0.5 ml Dulbecco's Modified Eagle's Medium (DMEM)-Ham's F-12 medium (1:1, vol/vol) containing 0.1 % bovine serum albumin (BSA, Sigma, St. Louis, MO), 0.1% Albumax (Gibco BRL, Gaithersburg, MD), 27.5 ?g/ml transferrin, 200 ng/ml insulin (human recombinant, Sigma), and 0.05 mg/ml L-ascorbic acid (Sigma) in a 4-well culture plate (Nunc plate, Applied Scientific, South San Francisco, CA). Medium was supplemented with penicillin and streptomycin to prevent bacterial contamination.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | About 20 ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO). Two independent RNA samples were analysed for each treatment group.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | chips were scanned using Agilent GeneArray Scanner G2500A
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using a scaling factor of 125, and then imported into the GeneSpring program (Agilent Technologies, Palo Alto, CA).
| Sample_platform_id | GPL85
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM237nnn/GSM237018/suppl/GSM237018.CEL.gz
| Sample_series_id | GSE9300
| Sample_data_row_count | 8799
| |
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