Search results for the GEO ID: GSE46426 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1130053 | GPL1261 |
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R26R^AC/AC (Control), biological replicate #1
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Mouse control_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC (Control)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
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Gene expression data from control PSM.
|
Sample_geo_accession | GSM1130053
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130053/suppl/GSM1130053_Control__1.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
|
GSM1130054 | GPL1261 |
|
R26R^AC/AC (Control), biological replicate #2
|
Mouse control_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC (Control)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
|
Gene expression data from control PSM.
|
Sample_geo_accession | GSM1130054
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130054/suppl/GSM1130054_Control__2.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
|
GSM1130055 | GPL1261 |
|
R26R^AC/AC (Control), biological replicate #3
|
Mouse control_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC (Control)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
|
Gene expression data from control PSM.
|
Sample_geo_accession | GSM1130055
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130055/suppl/GSM1130055_Control__3.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
|
GSM1130056 | GPL1261 |
|
R26R^AC/AC;T-Cre (Mutant), biological replicate #1
|
Mousemutant_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC;T-Cre (Mutant)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
|
Gene expression data from mutant PSM.
|
Sample_geo_accession | GSM1130056
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130056/suppl/GSM1130056_Mutant__1.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
|
GSM1130057 | GPL1261 |
|
R26R^AC/AC;T-Cre (Mutant), biological replicate #2
|
Mousemutant_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC;T-Cre (Mutant)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
|
Gene expression data from mutant PSM.
|
Sample_geo_accession | GSM1130057
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130057/suppl/GSM1130057_Mutant__2.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
|
GSM1130058 | GPL1261 |
|
R26R^AC/AC;T-Cre (Mutant), biological replicate #3
|
Mousemutant_PSM
|
strain background: C57BL6/6J
genotype/variation: R26R^AC/AC;T-Cre (Mutant)
developmental stage: E8.75
tissue: presomitic mesoderm (PSM)
|
Gene expression data from mutant PSM.
|
Sample_geo_accession | GSM1130058
| Sample_status | Public on Apr 27 2013
| Sample_submission_date | Apr 26 2013
| Sample_last_update_date | Apr 27 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | The anterior 2/3 PSM was dissected from the posterior 1/3 PSM and somites. Anterior PSM was briefly rinsed in 1X PBS (Gibco).
| Sample_growth_protocol_ch1 | Control and mutant embryos were harvested on Embronic day (E) 8.75 in L-15 media under a dissection light and fluorescent microscope setup.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | The anterior PSM was pipetted into lysis solution and underwent total RNA purification using the PicoPure RNA Isolation Kit (Life Technologies).
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared using the 3' IVT Express Kit (Affymetrix) for 1 ug total RNA according to the standard protocol for cRNA synthesis (GeneChip 3’ IVT Express Kit).
| Sample_hyb_protocol | Following fragmentation, 5.5 ug of cRNA was hybridized to Affymetrix Mouse 430 2.0 GeneChips for 16 hours at 45 °C. GeneChips were washed and stained using a fluidics station.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 3000. The images are analyzed using Affymetrix Command Console Viewer and metric analyses are carried out according to the instructions provided by Affymetrix using the Affymetrix Expression Console.
| Sample_data_processing | Data was acquired and normalized using Affymetrix Expression Console software under Affymetrix default analysis settings and global scaling as normalization method to generate Microarray Suite version 5.0 (MAS 5.0) files. Data is represented by presence/absence call for each gene using appropriate algorithms and expression data that had an “absent” call was filtered out of data sets using Excel software (Microsoft).
| Sample_platform_id | GPL1261
| Sample_contact_name | Timothy,Peter,Lopez
| Sample_contact_email | tpetelopez@gmail.com
| Sample_contact_laboratory | Chen-Ming Fan
| Sample_contact_department | Biology
| Sample_contact_institute | Johns Hopkins University/Carnegie Institution
| Sample_contact_address | 3520 San Martin Drive
| Sample_contact_city | Baltimore
| Sample_contact_state | Maryland
| Sample_contact_zip/postal_code | 21218
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1130nnn/GSM1130058/suppl/GSM1130058_Mutant__3.CEL.gz
| Sample_series_id | GSE46426
| Sample_data_row_count | 19606
| |
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