PureCN: copy number calling and SNV classification using targeted short read sequencing.

Riester, Markus; Singh, Angad P; Brannon, A Rose; Yu, Kun; Campbell, Catarina D; Chiang, Derek Y; Morrissey, Michael P

Riester, Markus; Singh, Angad P; Brannon, A Rose; Yu, Kun; Campbell, Catarina D; Chiang, Derek Y; Morrissey, Michael P.

Afiliação

Riester M; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Singh AP; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Brannon AR; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Yu K; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Campbell CD; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Chiang DY; Novartis Institutes for BioMedical Research, Cambridge, MA USA.
Morrissey MP; Novartis Institutes for BioMedical Research, Cambridge, MA USA.

Source Code Biol Med ; 11: 13, 2016.

Article em En | MEDLINE | ID: mdl-27999612

Palavras-chave

Cell lines; Copy number; Heterogeneity; Hybrid capture; Loss of heterozygosity; Ploidy; Purity; Whole exome sequencing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Source Code Biol Med Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido

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