Article

Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets

2017-03-22

Abstract excerpt

Somatic copy number variations (CNVs) play a crucial role in development of many human cancers. The broad availability of next-generation sequencing data has enabled the development of algorithms to computationally infer CNV profiles from a variety of data types including exome and targeted sequence data; currently the most prevalent types of cancer genomics data. However, systemic evaluation and comparison of the...

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Literature Corpus work: 84ad6bf6-1f50-5d7b-acff-28202fdf48c4
DOI: 10.1101/119636

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