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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...
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| Pubblicato in: | BMC Bioinformatics |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7890800/ https://ncbi.nlm.nih.gov/pubmed/33602113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-021-03995-y |
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