GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation

BACKGROUND: Variant interpretation is the main bottleneck in medical genomic sequencing efforts. This usually involves genome analysts manually searching through a multitude of independent databases, often with the aid of several, mostly independent, computational tools. To streamline variant interp...

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Detalles Bibliográficos
Autores principales: Manshaei, Roozbeh, DeLong, Sean, Andric, Veronica, Joshi, Esha, Okello, John B. A., Dhir, Priya, Somerville, Cherith, Farncombe, Kirsten M., Kalbfleisch, Kelsey, Jobling, Rebekah K., Scherer, Stephen W., Kim, Raymond H., Hosseini, S. Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857790/
https://www.ncbi.nlm.nih.gov/pubmed/35180879
http://dx.doi.org/10.1186/s12920-022-01166-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857790/
https://www.ncbi.nlm.nih.gov/pubmed/35180879
http://dx.doi.org/10.1186/s12920-022-01166-3

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