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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Detalles Bibliográficos
Autores principales: Tang, Man, Hasan, Mohammad Shabbir, Zhu, Hongxiao, Zhang, Liqing, Wu, Xiaowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Primary Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387560/
https://www.ncbi.nlm.nih.gov/pubmed/30795817
http://dx.doi.org/10.1186/s40246-019-0194-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387560/
https://www.ncbi.nlm.nih.gov/pubmed/30795817
http://dx.doi.org/10.1186/s40246-019-0194-6

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