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16GT: a fast and sensitive variant caller using a 16-genotype probabilistic model
16GT is a variant caller for Illumina whole-genome and whole-exome sequencing data. It uses a new 16-genotype probabilistic model to unify single nucleotide polymorphism and insertion and deletion calling in a single variant calling algorithm. In benchmark comparisons with 5 other widely used varian...
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| Udgivet i: | Gigascience |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5570013/ https://ncbi.nlm.nih.gov/pubmed/28637275 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/gigascience/gix045 |
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