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RFcaller: a machine learning approach combined with read-level features to detect somatic mutations
The cost reduction in sequencing and the extensive genomic characterization of a wide variety of cancers are expanding tumor sequencing to a wide number of research groups and the clinical practice. Although specific pipelines have been generated for the identification of somatic mutations, their re...
Autores principales: | Díaz-Navarro, Ander, Bousquets-Muñoz, Pablo, Nadeu, Ferran, López-Tamargo, Sara, Beà, Silvia, Campo, Elias, Puente, Xose S |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227442/ https://www.ncbi.nlm.nih.gov/pubmed/37260508 http://dx.doi.org/10.1093/nargab/lqad056 |
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