SNVHMM: predicting single nucleotide variants from next generation sequencing

BACKGROUND: The rapid development of next generation sequencing (NGS) technology provides a novel avenue for genomic exploration and research. Single nucleotide variants (SNVs) inferred from next generation sequencing are expected to reveal gene mutations in cancer. However, NGS has lower sequence c...

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Detalles Bibliográficos
Autores principales: Bian, Jiawen, Liu, Chenglin, Wang, Hongyan, Xing, Jing, Kachroo, Priyanka, Zhou, Xiaobo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718670/
https://www.ncbi.nlm.nih.gov/pubmed/23855743
http://dx.doi.org/10.1186/1471-2105-14-225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718670/
https://www.ncbi.nlm.nih.gov/pubmed/23855743
http://dx.doi.org/10.1186/1471-2105-14-225

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