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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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Bibliografische gegevens
Gepubliceerd in:Pac Symp Biocomput
Hoofdauteurs: Anand, Shankara, Kalesinskas, Laurynas, Smail, Craig, Tanigawa, Yosuke
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2019
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6417821/
https://ncbi.nlm.nih.gov/pubmed/30864321
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