Investigating low frequency variants in CAD/MI cases, controls and pedigrees using whole exome sequencing and custom pulldowns
Investigating low frequency variants in CAD/MI cases, controls and pedigrees using whole exome sequencing and custom pulldowns
- 27/04/2017
- 12 samples
- DAC: EGAC00001000103
- Technology: Illumina HiSeq 2000
Wellcome Trust Sanger Institute Data Sharing Policy
https://www.sanger.ac.uk/datasharing/
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 |
|---|---|---|
| EGAS00001000043 | 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 | Quality Report |
Located in
i
|
|---|---|---|---|---|
| EGAF00000078915 | bam | 13.5 GB | Report |
|
| EGAF00000078916 | bam | 12.8 GB | Report |
|
| EGAF00000078917 | bam | 12.9 GB | Report |
|
| EGAF00000078918 | bam | 13.3 GB | Report |
|
| EGAF00000078919 | bam | 13.3 GB | Report |
|
| EGAF00000078920 | bam | 13.4 GB | Report |
|
| EGAF00000078921 | bam | 13.6 GB | Report |
|
| EGAF00000078922 | bam | 17.3 GB | Report |
|
| EGAF00000078923 | bam | 16.1 GB | Report |
|
| EGAF00000078924 | bam | 17.1 GB | Report |
|
| EGAF00000078925 | bam | 17.0 GB | Report |
|
| EGAF00000081183 | bam | 14.4 GB | Report |
|
| 12 Files (174.7 GB) | ||||