Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.

Nucleic Acids Res · 2016 · PMC5772337 · PMID 27260798

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highly significantno p-value reported

The method used in this work has allowed us discover both known and novel cancer predisposing CNVRs, but the highly significant CNVRs might still contain copy number polymorphism.

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