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A probabilistic method for the detection and genotyping of small indels from population-scale sequence data
Motivation: High-throughput sequencing technologies have made population-scale studies of human genetic variation possible. Accurate and comprehensive detection of DNA sequence variants is crucial for the success of these studies. Small insertions and deletions represent the second most frequent cla...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3137221/ https://ncbi.nlm.nih.gov/pubmed/21653520 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr344 |
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