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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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Pac Symp Biocomput
Main Authors: Anand, Shankara, Kalesinskas, Laurynas, Smail, Craig, Tanigawa, Yosuke
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6417821/
https://ncbi.nlm.nih.gov/pubmed/30864321
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