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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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| I publikationen: | Bioinformatics |
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| Huvudupphovsman: | |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2016
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| Ämnen: | |
| Länkar: | 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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