Inferring phenotypes from substance use via collaborative matrix completion

BACKGROUND: Although substance use disorders (SUDs) are heritable, few genetic risk factors for them have been identified, in part due to the small sample sizes of study populations. To address this limitation, researchers have aggregated subjects from multiple existing genetic studies, but these su...

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Detalles Bibliográficos
Autores principales: Lu, Jin, Sun, Jiangwen, Wang, Xinyu, Kranzler, Henry, Gelernter, Joel, Bi, Jinbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249733/
https://www.ncbi.nlm.nih.gov/pubmed/30463556
http://dx.doi.org/10.1186/s12918-018-0623-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249733/
https://www.ncbi.nlm.nih.gov/pubmed/30463556
http://dx.doi.org/10.1186/s12918-018-0623-5

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