Var∣Decrypt: a novel and user-friendly tool to explore and prioritize variants in whole-exome sequencing data

BACKGROUND: High-throughput sequencing (HTS) offers unprecedented opportunities for the discovery of causative gene variants in multiple human disorders including cancers, and has revolutionized clinical diagnostics. However, despite more than a decade of use of HTS-based assays, extracting relevant...

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Detalles Bibliográficos
Autores principales: Salma, Mohammad, Alaterre, Elina, Moreaux, Jérôme, Soler, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265870/
https://www.ncbi.nlm.nih.gov/pubmed/37312221
http://dx.doi.org/10.1186/s13072-023-00497-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265870/
https://www.ncbi.nlm.nih.gov/pubmed/37312221
http://dx.doi.org/10.1186/s13072-023-00497-4

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