Methylation risk scores are associated with a collection of phenotypes within electronic health record systems

Inference of clinical phenotypes is a fundamental task in precision medicine, and has therefore been heavily investigated in recent years in the context of electronic health records (EHR) using a large arsenal of machine learning techniques, as well as in the context of genetics using polygenic risk...

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Detalles Bibliográficos
Autores principales: Thompson, Mike, Hill, Brian L., Rakocz, Nadav, Chiang, Jeffrey N., Geschwind, Daniel, Sankararaman, Sriram, Hofer, Ira, Cannesson, Maxime, Zaitlen, Noah, Halperin, Eran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411568/
https://www.ncbi.nlm.nih.gov/pubmed/36008412
http://dx.doi.org/10.1038/s41525-022-00320-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411568/
https://www.ncbi.nlm.nih.gov/pubmed/36008412
http://dx.doi.org/10.1038/s41525-022-00320-1

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