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Evaluating the accuracy of variant calling methods using the frequency of parent‐offspring genotype mismatch
The use of next‐generation sequencing (NGS) data sets has increased dramatically over the last decade, but there have been few systematic analyses quantifying the accuracy of the commonly used variant caller programs. Here we used a familial design consisting of diploid tissue from a single lodgepol...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544674/ https://www.ncbi.nlm.nih.gov/pubmed/35510784 http://dx.doi.org/10.1111/1755-0998.13628 |