eDiVA—Classification and prioritization of pathogenic variants for clinical diagnostics

Mendelian diseases have shown to be an and efficient model for connecting genotypes to phenotypes and for elucidating the function of genes. Whole‐exome sequencing (WES) accelerated the study of rare Mendelian diseases in families, allowing for directly pinpointing rare causal mutations in genic reg...

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Detalles Bibliográficos
Autores principales: Bosio, Mattia, Drechsel, Oliver, Rahman, Rubayte, Muyas, Francesc, Rabionet, Raquel, Bezdan, Daniela, Domenech Salgado, Laura, Hor, Hyun, Schott, Jean‐Jacques, Munell, Francina, Colobran, Roger, Macaya, Alfons, Estivill, Xavier, Ossowski, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Informatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767450/
https://www.ncbi.nlm.nih.gov/pubmed/31026367
http://dx.doi.org/10.1002/humu.23772

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767450/
https://www.ncbi.nlm.nih.gov/pubmed/31026367
http://dx.doi.org/10.1002/humu.23772

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