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vi-HMM: a novel HMM-based method for sequence variant identification in short-read data
Abstract Background Accurate and reliable identification of sequence variants, including single nucleotide polymorphisms (SNPs) and insertion-deletion polymorphisms (INDELs), plays a fundamental role in next-generation sequencing (NGS) applications. Existing methods for calling these variants often...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMC
2019-02-01
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| Serier: | Human Genomics |
| Fag: | |
| Online adgang: | http://link.springer.com/article/10.1186/s40246-019-0194-6 |
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