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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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| Publicado no: | BMC Syst Biol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | 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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