Search results for the GEO ID: GSE26750 |
(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 |
GSM658325 | GPL1261 |
|
Granule cell layer animal1-1
|
Cerebellum of 8-week-old C57BL/6J male
|
strain: C57BL/6J
gender: male
age: 8-week-old
tissue: Cerebellum
cell type: cerebellar granule cell layer
|
Gene expression data from mouse cerebellar granule cell layer
|
Sample_geo_accession | GSM658325
| Sample_status | Public on Jan 17 2013
| Sample_submission_date | Jan 20 2011
| Sample_last_update_date | Jan 17 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Brains were rapidly removed and frozen in liquid nitrogen-chilled isopentane, and then stored at -80 ºC. Brains were sagittally sectioned at 12 μm thickness using cryostat at -20 ºC. Sections were fixed with a mixture of ethanol/acetic acid (19:1) on dry ice and dried out. Cells were cut using laser capture microdissection
| Sample_growth_protocol_ch1 | Intact 8-week-old mice were used
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were dissolved in RNA extraction buffer and stored at -80 ºC according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNAs were synthesized from mRNAs in approximately 1 ng of total RNA, amplified and labeled, according to standard protocols of Affymetrix GeneChip Expression Analysis (GeneChip Two-Cycle Target Labeling, Control Reagents, Affymetrix).
| Sample_hyb_protocol | The samples were hybridized to DNA microarray, according to standard protocols of Affymetrix GeneChip Expression Analysis (Mouse Genome 430 2.0 Array, GeneChip Hybridization, Wash and Stain Kit, Affymetrix).
| Sample_scan_protocol | GeneChips were scanned using GeneChip Scanner 3000 7G.
| Sample_data_processing | A dataset of each sample was analyzed with GeneChip Operating Software (GCOS 1, Affymetrix). The present (P), marginal (M), or absent (A) call for each data point was calculated by the standard algorithm. Each probe set contained 11 probes. Here, we chose 26,351 probe sets, corresponding to 17,197 genes, each of which contained more than nine probes matched to the defined cDNAs having gene symbols in the ENSEMBL or NCBI (reference sequence) database, and used them for further analysis.
| Sample_platform_id | GPL1261
| Sample_contact_name | Nozomu,H,Nakamura
| Sample_contact_email | nakamun@gmail.com
| Sample_contact_department | Molecular Neuroscience Unit
| Sample_contact_institute | Okinawa Institute of Science and Technology
| Sample_contact_address | 12-22 Suzaki
| Sample_contact_city | Uruma
| Sample_contact_state | Okinawa
| Sample_contact_zip/postal_code | 904-2234
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM658nnn/GSM658325/suppl/GSM658325.CEL.gz
| Sample_series_id | GSE26750
| Sample_series_id | GSE26751
| Sample_data_row_count | 45101
| |
|
GSM658326 | GPL1261 |
|
Granule cell layer animal1-2
|
Cerebellum of 8-week-old C57BL/6J male
|
strain: C57BL/6J
gender: male
age: 8-week-old
tissue: Cerebellum
cell type: cerebellar granule cell layer
|
Gene expression data from mouse cerebellar granule cell layer
|
Sample_geo_accession | GSM658326
| Sample_status | Public on Jan 17 2013
| Sample_submission_date | Jan 20 2011
| Sample_last_update_date | Jan 17 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Brains were rapidly removed and frozen in liquid nitrogen-chilled isopentane, and then stored at -80 ºC. Brains were sagittally sectioned at 12 μm thickness using cryostat at -20 ºC. Sections were fixed with a mixture of ethanol/acetic acid (19:1) on dry ice and dried out. Cells were cut using laser capture microdissection
| Sample_growth_protocol_ch1 | Intact 8-week-old mice were used
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were dissolved in RNA extraction buffer and stored at -80 ºC according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNAs were synthesized from mRNAs in approximately 1 ng of total RNA, amplified and labeled, according to standard protocols of Affymetrix GeneChip Expression Analysis (GeneChip Two-Cycle Target Labeling, Control Reagents, Affymetrix).
| Sample_hyb_protocol | The samples were hybridized to DNA microarray, according to standard protocols of Affymetrix GeneChip Expression Analysis (Mouse Genome 430 2.0 Array, GeneChip Hybridization, Wash and Stain Kit, Affymetrix).
| Sample_scan_protocol | GeneChips were scanned using GeneChip Scanner 3000 7G.
| Sample_data_processing | A dataset of each sample was analyzed with GeneChip Operating Software (GCOS 1, Affymetrix). The present (P), marginal (M), or absent (A) call for each data point was calculated by the standard algorithm. Each probe set contained 11 probes. Here, we chose 26,351 probe sets, corresponding to 17,197 genes, each of which contained more than nine probes matched to the defined cDNAs having gene symbols in the ENSEMBL or NCBI (reference sequence) database, and used them for further analysis.
| Sample_platform_id | GPL1261
| Sample_contact_name | Nozomu,H,Nakamura
| Sample_contact_email | nakamun@gmail.com
| Sample_contact_department | Molecular Neuroscience Unit
| Sample_contact_institute | Okinawa Institute of Science and Technology
| Sample_contact_address | 12-22 Suzaki
| Sample_contact_city | Uruma
| Sample_contact_state | Okinawa
| Sample_contact_zip/postal_code | 904-2234
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM658nnn/GSM658326/suppl/GSM658326.CEL.gz
| Sample_series_id | GSE26750
| Sample_series_id | GSE26751
| Sample_data_row_count | 45101
| |
|
|
|
Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
|
|
|
Select expression type |
Transcripts profile based on; |
A. Differential status (Up/Down regulation) |
|
|
Regulation type |
|
Fold change |
|
p-value |
|
|
|
B. Absolute calls (Transcribed/Not-detected) |
|
|
Derive calls within/across groups |
Within groups |
|
|
Detection status |
|
Percentage detection |
|
|
Across groups |
|
|
Detection status |
First group: |
- |
Second group:
|
Percentage detection |
First group: |
- |
Second group:
|
|
|
|
Filter results by number of probes |
|
|