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Phenotype-driven gene prioritization for rare diseases using graph convolution on heterogeneous networks
BACKGROUND: One of the major goals of genomic medicine is the identification of causal genomic variants in a patient and their relation to the observed clinical phenotypes. Prioritizing the genomic variants by considering only the genotype information usually identifies a few hundred potential varia...
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| Publicado no: | BMC Med Genomics |
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| 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/PMC6035401/ https://ncbi.nlm.nih.gov/pubmed/29980210 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-018-0372-8 |
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