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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...
Autores principales: | Sedlazeck, Fritz Joachim, Talloji, Prabhavathi, von Haeseler, Arndt, Bachmair, Andreas |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2013
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Materias: | |
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 |
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