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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...

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Detalles Bibliográficos
Autores principales: Díaz-Navarro, Ander, Bousquets-Muñoz, Pablo, Nadeu, Ferran, López-Tamargo, Sara, Beà, Silvia, Campo, Elias, Puente, Xose S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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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