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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)

1 Dataset 2 Publications

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	1006 Familial early onset gemrline CRC patients sequenced by the Molecular and Population Genetics group of the Institute of Cancer Research	Illumina HiSeq 2500	1006

Publications	Citations
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer. Chubb D, Broderick P, Dobbins SE, Frampton M, Kinnersley B, Penegar S, Price A, Ma YP, Sherborne AL, Palles C, Timofeeva MN, Bishop DT, Dunlop MG, Tomlinson I, Houlston RS. Nat Commun 7: 2016 11883	93
CanVar: A resource for sharing germline variation in cancer patients. Chubb D, Broderick P, Dobbins SE, Houlston RS. F1000Res 5: 2016 2813	8