sWGS for genome-wide copy number profiling

Dataset ID Technology Samples
EGAD00001006384 Illumina MiSeq,NextSeq 550 45

Dataset Description

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 metastatic colorectal cancer patients (mCRC).

Data Use Conditions


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