Large scale familial CRC exome sequencing study
The burden of rare disruptive mutations to the heritable risk of colorectal cancer
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
---|---|---|---|
EGAD00001002204 | Illumina HiSeq 2500 | 1006 |
Publications | Citations |
---|---|
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
Nat Commun 7: 2016 11883 |
92 |
CanVar: A resource for sharing germline variation in cancer patients.
F1000Res 5: 2016 2813 |
6 |