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SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPs
Genetic variations of the human genome are linked to many disease phenotypes. While whole-genome sequencing and genome-wide association studies (GWAS) have uncovered a number of genotype-phenotype associations, their functional interpretation remains challenging given most single nucleotide polymorp...
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| Publié dans: | Pac Symp Biocomput |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6417821/ https://ncbi.nlm.nih.gov/pubmed/30864321 |
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