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Large scale familial CRC exome sequencing study

The burden of rare disruptive mutations to the heritable risk of colorectal cancer

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