sWGS of CRC patients

Dataset ID Technology Samples
EGAD00001006101 Illumina MiSeq,NextSeq 550 52

Dataset Description

Paired end (47/98) and single end (51/98) shallow whole genome sequencing (sWGS) data for the identification of somatic copy number alterations (SCNA) and the estimation of tumor fractions in plasma DNA of colorectal cancer (CRC) patients.

Data Use Conditions


See further information on Data Use Conditions

Label Code Version Modifier
disease specific research DUO:0000007 2019-01-07 MONDO:0005575