High-throughput screening of prostate cancer risk loci by single nucleotide polymorphisms sequencing

Functional characterization of disease-causing variants at risk loci has been a significant challenge. Here we report a high-throughput single-nucleotide polymorphisms sequencing (SNPs-seq) technology to simultaneously screen hundreds to thousands of SNPs for their allele-dependent protein-binding d...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Nat Commun
Main Authors: Zhang, Peng, Xia, Ji-Han, Zhu, Jing, Gao, Ping, Tian, Yi-Jun, Du, Meijun, Guo, Yong-Chen, Suleman, Sufyan, Zhang, Qin, Kohli, Manish, Tillmans, Lori S., Thibodeau, Stephen N., French, Amy J., Cerhan, James R., Wang, Li-Dong, Wei, Gong-Hong, Wang, Liang
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2018
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5964124/
https://ncbi.nlm.nih.gov/pubmed/29789573
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-04451-x
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados