Transcript expression-aware annotation improves rare variant interpretation

The acceleration of DNA sequencing in samples from patients and population studies has resulted in extensive catalogues of human genetic variation, but the interpretation of rare genetic variants remains problematic. A notable example of this challenge is the existence of disruptive variants in dosa...

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Detalles Bibliográficos
Autores principales: Cummings, Beryl B., Karczewski, Konrad J., Kosmicki, Jack A., Seaby, Eleanor G., Watts, Nicholas A., Singer-Berk, Moriel, Mudge, Jonathan M., Karjalainen, Juha, Satterstrom, F. Kyle, O’Donnell-Luria, Anne H., Poterba, Timothy, Seed, Cotton, Solomonson, Matthew, Alföldi, Jessica, Daly, Mark J., MacArthur, Daniel G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334198/
https://www.ncbi.nlm.nih.gov/pubmed/32461655
http://dx.doi.org/10.1038/s41586-020-2329-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334198/
https://www.ncbi.nlm.nih.gov/pubmed/32461655
http://dx.doi.org/10.1038/s41586-020-2329-2

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