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FiNGS: high quality somatic mutations using filters for next generation sequencing
BACKGROUND: Somatic variant callers are used to find mutations in sequencing data from cancer samples. They are very sensitive and have high recall, but also may produce low precision data with a large proportion of false positives. Further ad hoc filtering is commonly performed after variant callin...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890800/ https://www.ncbi.nlm.nih.gov/pubmed/33602113 http://dx.doi.org/10.1186/s12859-021-03995-y |