Search results for the GEO ID: GSE43339 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1060690 | GPL1261 |
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Gene expression in DX5- NK
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Liver DX5- NK cells
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strain: B6
tissue: liver
cell type: DX5-NK1.1+CD3-
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Gene expression in DX5- NK
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Sample_geo_accession | GSM1060690
| Sample_status | Public on Jan 09 2013
| Sample_submission_date | Jan 08 2013
| Sample_last_update_date | Jan 09 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | DX5-NK1.1+CD3- cells and DX5+NK1.1+CD3- cells were sorted from the liver of naive B6 wild-type mice by FACS Aria.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted from each sample using Trizol (Qiagen) according to the manufacturer's protocol. RNA was then further purified using RNeasy Mini Kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cRNA were labeled by using One-Cycle Target Labeling and Control Reagents, Affymetrix, P/N 900493,and then purified by using QIAGEN RNeasy Total RNA Isolation kit.
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Mouse430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip® Scanner 3000.
| Sample_data_processing | Raw data were normalized by MAS 5.0 algorithm,GCOS1.4.
| Sample_platform_id | GPL1261
| Sample_contact_name | Hui,,Peng
| Sample_contact_institute | University of Science and Technology of China
| Sample_contact_address | 443 Huangshan Road
| Sample_contact_city | Hefei
| Sample_contact_zip/postal_code | 230027
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1060nnn/GSM1060690/suppl/GSM1060690_DX5-_NK.CEL.gz
| Sample_series_id | GSE43339
| Sample_data_row_count | 45101
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GSM1060691 | GPL1261 |
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Gene expression in DX5+ NK
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Liver DX5+ NK cells
|
strain: B6
tissue: liver
cell type: DX5+NK1.1+CD3-
|
Gene expression in DX5+ NK
|
Sample_geo_accession | GSM1060691
| Sample_status | Public on Jan 09 2013
| Sample_submission_date | Jan 08 2013
| Sample_last_update_date | Jan 09 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | DX5-NK1.1+CD3- cells and DX5+NK1.1+CD3- cells were sorted from the liver of naive B6 wild-type mice by FACS Aria.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted from each sample using Trizol (Qiagen) according to the manufacturer's protocol. RNA was then further purified using RNeasy Mini Kit (Qiagen).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cRNA were labeled by using One-Cycle Target Labeling and Control Reagents, Affymetrix, P/N 900493,and then purified by using QIAGEN RNeasy Total RNA Isolation kit.
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Mouse430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip® Scanner 3000.
| Sample_data_processing | Raw data were normalized by MAS 5.0 algorithm,GCOS1.4.
| Sample_platform_id | GPL1261
| Sample_contact_name | Hui,,Peng
| Sample_contact_institute | University of Science and Technology of China
| Sample_contact_address | 443 Huangshan Road
| Sample_contact_city | Hefei
| Sample_contact_zip/postal_code | 230027
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1060nnn/GSM1060691/suppl/GSM1060691_DX5+_NK.CEL.gz
| Sample_series_id | GSE43339
| Sample_data_row_count | 45101
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