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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Detalles Bibliográficos
Autores principales: Anand, Shankara, Kalesinskas, Laurynas, Smail, Craig, Tanigawa, Yosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417821/
https://www.ncbi.nlm.nih.gov/pubmed/30864321

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417821/
https://www.ncbi.nlm.nih.gov/pubmed/30864321

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