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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Detalles Bibliográficos
Autores principales: Sedlazeck, Fritz Joachim, Talloji, Prabhavathi, von Haeseler, Arndt, Bachmair, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580289/
https://www.ncbi.nlm.nih.gov/pubmed/23246509
http://dx.doi.org/10.1016/j.ygeno.2012.12.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580289/
https://www.ncbi.nlm.nih.gov/pubmed/23246509
http://dx.doi.org/10.1016/j.ygeno.2012.12.001

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