LitVar: a semantic search engine for linking genomic variant data in PubMed and PMC

The identification and interpretation of genomic variants play a key role in the diagnosis of genetic diseases and related research. These tasks increasingly rely on accessing relevant manually curated information from domain databases (e.g. SwissProt or ClinVar). However, due to the sheer volume of...

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Detalles Bibliográficos
Autores principales: Allot, Alexis, Peng, Yifan, Wei, Chih-Hsuan, Lee, Kyubum, Phan, Lon, Lu, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Web Server Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030971/
https://www.ncbi.nlm.nih.gov/pubmed/29762787
http://dx.doi.org/10.1093/nar/gky355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030971/
https://www.ncbi.nlm.nih.gov/pubmed/29762787
http://dx.doi.org/10.1093/nar/gky355

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