Comparison of genetic variants in matched samples using thesaurus annotation

<strong>Motivation:</strong> Calling changes in DNA, e.g. as a result of somatic events in cancer, requires analysis of multiple matched sequenced samples. Events in low-mappability regions of the human genome are difficult to encode in variant call files and have been under-reported as...

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Detalhes bibliográficos
Principais autores: Nijman, S, Konopka, T
Formato: Journal article
Publicado em: Oxford University Press 2015