Variant calling in low-coverage whole genome sequencing of a Native American population sample

BACKGROUND: The reduction in the cost of sequencing a human genome has led to the use of genotype sampling strategies in order to impute and infer the presence of sequence variants that can then be tested for associations with traits of interest. Low-coverage Whole Genome Sequencing (WGS) is a sampl...

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Detalhes bibliográficos
Main Authors: Bizon, Chris, Spiegel, Michael, Chasse, Scott A, Gizer, Ian R, Li, Yun, Malc, Ewa P, Mieczkowski, Piotr A, Sailsbery, Josh K, Wang, Xiaoshu, Ehlers, Cindy L, Wilhelmsen, Kirk C
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3914019/
https://ncbi.nlm.nih.gov/pubmed/24479562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-85
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