pyAmpli: an amplicon-based variant filter pipeline for targeted resequencing data

BACKGROUND: Haloplex targeted resequencing is a popular method to analyze both germline and somatic variants in gene panels. However, involved wet-lab procedures may introduce false positives that need to be considered in subsequent data-analysis. No variant filtering rationale addressing amplicon e...

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Detalles Bibliográficos
Autores principales: Beyens, Matthias, Boeckx, Nele, Van Camp, Guy, Op de Beeck, Ken, Vandeweyer, Geert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729461/
https://www.ncbi.nlm.nih.gov/pubmed/29237398
http://dx.doi.org/10.1186/s12859-017-1985-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729461/
https://www.ncbi.nlm.nih.gov/pubmed/29237398
http://dx.doi.org/10.1186/s12859-017-1985-1

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