Inferring Variation in Copy Number Using High Throughput Sequencing Data in R

Inference of copy number variation presents a technical challenge because variant callers typically require the copy number of a genome or genomic region to be known a priori. Here we present a method to infer copy number that uses variant call format (VCF) data as input and is implemented in the R...

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Detalles Bibliográficos
Autores principales: Knaus, Brian J., Grünwald, Niklaus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909048/
https://www.ncbi.nlm.nih.gov/pubmed/29706990
http://dx.doi.org/10.3389/fgene.2018.00123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909048/
https://www.ncbi.nlm.nih.gov/pubmed/29706990
http://dx.doi.org/10.3389/fgene.2018.00123

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