Ena-DATASET-UH-tumorgenomics-02-04-2019-10:42:45:666-263 - samples

ABSTRACT: The data consists of 47 exome-sequenced synchronous colorectal cancers from 23 patients. The exomes of corresponding normal samples were used to remove germline variants. All patients are Finnish (white Caucasian). All except one patient (sync_11 who belongs to a LS family) were assumed sporadic. The sequence data was produced with Illumina HiSeq 4000.

PROVIDER: EGAD00001004884 | EGA |

REPOSITORIES: EGA