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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914019/
https://www.ncbi.nlm.nih.gov/pubmed/24479562
http://dx.doi.org/10.1186/1471-2164-15-85

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914019/
https://www.ncbi.nlm.nih.gov/pubmed/24479562
http://dx.doi.org/10.1186/1471-2164-15-85

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