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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...
Autores principales: | Beyens, Matthias, Boeckx, Nele, Van Camp, Guy, Op de Beeck, Ken, Vandeweyer, Geert |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
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 |
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