Search results for the GEO ID: GSE23724 |
(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 |
GSM585541 | GPL1261 |
|
skin.wt.replicate4
|
dorsal skin from GR+/+ E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR+/+
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR+/+ E18.5 embryos.
|
Sample_geo_accession | GSM585541
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585541/suppl/GSM585541.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585542 | GPL1261 |
|
skin.wt.replicate6
|
dorsal skin from GR+/+ E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR+/+
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR+/+ E18.5 embryos.
|
Sample_geo_accession | GSM585542
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585542/suppl/GSM585542.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585543 | GPL1261 |
|
skin.wt.replicate28
|
dorsal skin from GR+/+ E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR+/+
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR+/+ E18.5 embryos.
|
Sample_geo_accession | GSM585543
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585543/suppl/GSM585543.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585544 | GPL1261 |
|
skin.wt.replicate29
|
dorsal skin from GR+/+ E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR+/+
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR+/+ E18.5 embryos.
|
Sample_geo_accession | GSM585544
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585544/suppl/GSM585544.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585545 | GPL1261 |
|
skin.KO.replicate5
|
dorsal skin from GR-/- E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR-/-
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR-/- E18.5 embryos.
|
Sample_geo_accession | GSM585545
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585545/suppl/GSM585545.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585546 | GPL1261 |
|
skin.KO.replicate17
|
dorsal skin from GR-/- E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR-/-
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR-/- E18.5 embryos.
|
Sample_geo_accession | GSM585546
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585546/suppl/GSM585546.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585547 | GPL1261 |
|
skin.KO.replicate25
|
dorsal skin from GR-/- E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR-/-
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR-/- E18.5 embryos.
|
Sample_geo_accession | GSM585547
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585547/suppl/GSM585547.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
GSM585548 | GPL1261 |
|
skin.KO.replicate26
|
dorsal skin from GR-/- E18.5 embryo
|
tissue: dorsal skin
genotype/variation: GR-/-
strain: B6D2/F1
age: E18.5
|
Gene expression data from dorsal skin of GR-/- E18.5 embryos.
|
Sample_geo_accession | GSM585548
| Sample_status | Public on Aug 21 2010
| Sample_submission_date | Aug 20 2010
| Sample_last_update_date | Aug 23 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | GR-/- and GR+/+ embryo littermates were obtained by cesarean derivation at 18.5 days post-conception (the morning of the day that the vaginal plug was seen was considered as day 0.5).
| Sample_growth_protocol_ch1 | Mice were housed in standard temperature and humidity conditions and animal experimentation was conducted with accepted standards of humane animal care in our animal facility (Instituto de Biomedicina de Valencia IBV-CSIC).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was obtained using the RNeasy RNA extraction kit (Qiagen, Valencia, CA). RNA integrity was tested using the Bioanalyzer 2100 (Agilent Technologies).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Starting from an average of 5 mg total RNA, cDNA was synthesized and purified (one cycle cDNA synthesis Affy). cRNA was then biotin-labeled and purified (IVT Affy kit). After quantitation of the biotinylated cRNA, it was fragmented to perform the hybridization step as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_hyb_protocol | 15 mg of fragmented cRNA were used for each sample and hybridization performed as described on the webpage of the genomic platform at the Centro de Investigación del Cáncer de Salamanca (http://ubioinfo.cicancer.org).
| Sample_scan_protocol | GeneChips were scanned using a GenePix 4000B scanner (Molecular Devices, Sunnyvale, CA).
| Sample_data_processing | Probe set intensity values were summarized and normalized according to the RMA method using R and BioC.
| Sample_platform_id | GPL1261
| Sample_contact_name | Paloma,,Perez
| Sample_contact_email | pperez@ibv.csic.es
| Sample_contact_laboratory | Animal Models for Skin Pathology
| Sample_contact_institute | Instituto Biomedicina Valencia, Consejo Superior Investigaciones Científicas
| Sample_contact_address | Jaime Roig 11
| Sample_contact_city | Valencia
| Sample_contact_zip/postal_code | 46010
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM585nnn/GSM585548/suppl/GSM585548.CEL.gz
| Sample_series_id | GSE23724
| Sample_data_row_count | 45101
| |
|
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