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BGT: efficient and flexible genotype query across many samples

Summary: BGT is a compact format, a fast command line tool and a simple web application for efficient and convenient query of whole-genome genotypes and frequencies across tens to hundreds of thousands of samples. On real data, it encodes the haplotypes of 32 488 samples across 39.2 million SNPs int...

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書目詳細資料
發表在:Bioinformatics
主要作者: Li, Heng
格式: Artigo
語言:Inglês
出版: Oxford University Press 2016
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5963361/
https://ncbi.nlm.nih.gov/pubmed/26500154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv613
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