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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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| Publicado no: | Front Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5909048/ https://ncbi.nlm.nih.gov/pubmed/29706990 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00123 |
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