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SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
We develop a statistical tool SNVer for calling common and rare variants in analysis of pooled or individual next-generation sequencing (NGS) data. We formulate variant calling as a hypothesis testing problem and employ a binomial–binomial model to test the significance of observed allele frequency...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201884/ https://www.ncbi.nlm.nih.gov/pubmed/21813454 http://dx.doi.org/10.1093/nar/gkr599 |