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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Chen, Wei, Li, Bingshan, Zeng, Zhen, Sanna, Serena, Sidore, Carlo, Busonero, Fabio, Kang, Hyun Min, Li, Yun, Abecasis, Gonçalo R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Cold Spring Harbor Laboratory Press 2013
Gaiak:
Method
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3530674/
https://ncbi.nlm.nih.gov/pubmed/23064751
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.142455.112
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