I am using HCC1153 and HCC1954 from TCGA Mutation/Variation Calling Benchmark 4 for benchmarking SCNA calling. However, I found some SCNAs reported by COSMIC are germline CNVs (both tumor and normal sample has 0 copy (no reads) by viewing bams with IGV). Can anyone tell me how can I find the ground truth set of SCNAs for these two samples?
Question: Are all CNAs of HCC1153 cell line reported by COSMIC somatic mutations?
3.1 years ago by
lyz10302012 • 330
lyz10302012 • 330 wrote:
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