Genotype calling and haplotyping in parent-offspring trios

Emerging sequencing technologies allow common and rare variants to be systematically assayed across the human genome in many individuals. In order to improve variant detection and genotype calling, raw sequence data are typically examined across many individuals. Here, we describe a method for genot...

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Detalles Bibliográficos
Autores principales: Chen, Wei, Li, Bingshan, Zeng, Zhen, Sanna, Serena, Sidore, Carlo, Busonero, Fabio, Kang, Hyun Min, Li, Yun, Abecasis, Gonçalo R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530674/
https://www.ncbi.nlm.nih.gov/pubmed/23064751
http://dx.doi.org/10.1101/gr.142455.112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530674/
https://www.ncbi.nlm.nih.gov/pubmed/23064751
http://dx.doi.org/10.1101/gr.142455.112

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