Search results for the GEO ID: GSE13635 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM343471 | GPL1261 |
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Relative gene expression value from wildtype 1 retinas at birth
|
Pool of Wildtype 1 neonates retinas
|
Relative gene expression value from wildtype retinas at birth
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343471
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343471/suppl/GSM343471.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343471/suppl/GSM343471.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
|
GSM343472 | GPL1261 |
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Relative gene expression value from wildtype 2 retinas at birth
|
Pool of Wildtype 2 neonates retinas
|
Relative gene expression value from wildtype retinas at birth
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343472
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343472/suppl/GSM343472.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343472/suppl/GSM343472.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
|
GSM343473 | GPL1261 |
|
Relative gene expression value from wildtype 3 retinas at birth
|
Pool of Wildtype 3 neonates retinas
|
Relative gene expression value from wildtype retinas at birth
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343473
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343473/suppl/GSM343473.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343473/suppl/GSM343473.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
|
GSM343474 | GPL1261 |
|
Relative gene expression value from Cyclin D1 -/- 1 retinas at birth
|
Pool of Cyclin D1 -/- 1 neonates retinas
|
C57BL/6 129SV Mixed genetic background
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343474
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343474/suppl/GSM343474.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343474/suppl/GSM343474.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
|
GSM343475 | GPL1261 |
|
Relative gene expression value from Cyclin D1 -/- 2 retinas at birth
|
Pool of Cyclin D1 -/- 2 neonates retinas
|
C57BL/6 129SV Mixed genetic background
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343475
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343475/suppl/GSM343475.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343475/suppl/GSM343475.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
|
GSM343476 | GPL1261 |
|
Relative gene expression value from Cyclin D1 -/- 3 retinas at birth
|
Pool of Cyclin D1 -/- 3 neonates retinas
|
C57BL/6 129SV Mixed genetic background
|
The dataset was analyzed for statistically significant differential expression using the online NIA Array Analysis Tool REF (http://lgsun.grc.nia.nih.gov/ANOVA/).
Probesets were tested for differential expression using the following settings:
Threshold z-value to remove outliers: 10000
Error Model: Max(Average, Bayesian)
Error variance averaging window: 200
Proportion of highest error variances to be removed: 0.01
Bayesian degrees of freedom: 5
FDR threshold: 0.10
Probesets that did not map to genes for which we had cyclin D1 binding data and probesets that mapped to multiple genes were excluded. In the cases where multiple probesets map to one gene, the probeset with the largest differential expression was retained.
|
Sample_geo_accession | GSM343476
| Sample_status | Public on Jan 29 2010
| Sample_submission_date | Nov 18 2008
| Sample_last_update_date | Jan 29 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Homemade
| Sample_treatment_protocol_ch1 | Retina extraction in 1x PBS under binoccular
| Sample_growth_protocol_ch1 | Normal mouse breeding in state-of-the-art mouse facility.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy mini extraction kit
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated antisense cRNA probes were prepared according to the Affymetrix standard labeling protocol (one amplification round).
| Sample_hyb_protocol | Biotinylated cRNA was hybridized to Affymetrix GeneChip Mouse Expression Set 430 2.0 arrays at the Microarray Core Facility (Dana-Farber Cancer Institute).
| Sample_scan_protocol | Arrays were stained, scanned, and quantified according to standard Affymetrix protocols. Data were annotated according the NetAffx database (http://www.affymetrix.com/analysis/index.affx) as of March, 2006.
| Sample_data_processing | Quantile normalization was performed, and expression data were ranked within each sample. Within each sample, each probeset was given a signal value of the average signal of the probesets of that rank, across the dataset.
| Sample_platform_id | GPL1261
| Sample_contact_name | Frederic,Emile,Bienvenu
| Sample_contact_email | frederic_bienvenu@dfci.harvard.edu
| Sample_contact_phone | 617 632 3638
| Sample_contact_fax | 617 632 5006
| Sample_contact_laboratory | Sicinski
| Sample_contact_department | Cancer Biology
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 1 Jimmy Fund Way
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343476/suppl/GSM343476.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM343nnn/GSM343476/suppl/GSM343476.dcp.gz
| Sample_series_id | GSE13635
| Sample_series_id | GSE13636
| Sample_data_row_count | 45101
| |
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