Whole exome sequencing for HELIC
The HELIC study has been whole genome sequencing individuals from 2 Greek isolatedpopulations at 1x depth. The genotype calling process crucially involves a VQSR stepfollowed by imputation-based refinement. We have been investigating optimal ways toincrease calling accuracy. To aid us in setting appropriate parameters for VQSR and otherQC steps, we have carried out whole exome sequencing of a small number ofHELIC samples.
- 12/11/2015
- 5 samples
- DAC: EGAC00001000205
- Technology: Illumina HiSeq 2000
Wellcome Trust Sanger Institute Data Sharing Policy
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| Other |
This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.
| ID | File Type | Size | Located in | |
|---|---|---|---|---|
| EGAF00000507243 | cram | 1.7 GB | ||
| EGAF00000507244 | cram | 1.8 GB | ||
| EGAF00000507245 | cram | 1.6 GB | ||
| EGAF00000507246 | cram | 1.4 GB | ||
| EGAF00000507247 | cram | 1.6 GB | ||
| EGAF00000508780 | cram | 1.7 GB | ||
| EGAF00000508781 | cram | 1.7 GB | ||
| EGAF00000508782 | cram | 1.5 GB | ||
| EGAF00000508783 | cram | 1.4 GB | ||
| EGAF00000508784 | cram | 1.6 GB | ||
| 10 Files (15.9 GB) | ||||