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Benefit-of-doubt (BOD) scoring: A sequencing-based method for SNP candidate assessment from high to medium read number data sets

Identification of single nucleotide polymorphisms (SNPs) is a key element in sequence-based genetic analysis. Next generation sequencing offers a cost-effective basis to generate the necessary, large sequence data sets, and bioinformatic methods are being developed to process sequencing machine read...

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Detalhes bibliográficos
Main Authors: Sedlazeck, Fritz Joachim, Talloji, Prabhavathi, von Haeseler, Arndt, Bachmair, Andreas
Formato: Artigo
Idioma:Inglês
Publicado em: Academic Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3580289/
https://ncbi.nlm.nih.gov/pubmed/23246509
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2012.12.001
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