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vi-HMM: a novel HMM-based method for sequence variant identification in short-read data
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 make sim...
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| 發表在: | Hum Genomics |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2019
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6387560/ https://ncbi.nlm.nih.gov/pubmed/30795817 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-019-0194-6 |
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