A computational method for genotype calling in family-based sequencing data

BACKGROUND: As sequencing technologies can help researchers detect common and rare variants across the human genome in many individuals, it is known that jointly calling genotypes across multiple individuals based on linkage disequilibrium (LD) can facilitate the analysis of low to modest coverage s...

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Vydáno v:BMC Bioinformatics
Hlavní autoři: Chang, Lun-Ching, Li, Bingshan, Fang, Zhou, Vrieze, Scott, McGue, Matt, Iacono, William G., Tseng, George C., Chen, Wei
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Methodology Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4715317/
https://ncbi.nlm.nih.gov/pubmed/26772743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-0880-5
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