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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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| Veröffentlicht in: | BMC Syst Biol |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
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| Schlagworte: | |
| Online Zugang: | 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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