Single-Nucleotide Polymorphisms Sequencing Identifies Candidate Functional Variants at Prostate Cancer Risk Loci

Genome-wide association studies have identified over 150 risk loci that increase prostate cancer risk. However, few causal variants and their regulatory mechanisms have been characterized. In this study, we utilized our previously developed single-nucleotide polymorphisms sequencing (SNPs-seq) techn...

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Detalles Bibliográficos
Autores principales: Zhang, Peng, Tillmans, Lori S., Thibodeau, Stephen N., Wang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678189/
https://www.ncbi.nlm.nih.gov/pubmed/31323811
http://dx.doi.org/10.3390/genes10070547

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678189/
https://www.ncbi.nlm.nih.gov/pubmed/31323811
http://dx.doi.org/10.3390/genes10070547

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