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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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| Опубликовано в: : | BMC Syst Biol |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6249733/ https://ncbi.nlm.nih.gov/pubmed/30463556 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12918-018-0623-5 |
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