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High-throughput screening of prostate cancer risk loci by single nucleotide polymorphisms sequencing
Autor:
Zhang, P. (Peng), Xia, J.-H. (Ji-Han), Zhu, J. (Jing), Gao, P. (Ping), Tian, Y.-J. (Yi-Jun), Du, M. (Meijun), Guo, Y.-C. (Yong-Chen), Suleman, S. (Sufyan), Zhang, Q. (Qin), Kohli, M. (Manish), Tillmans, L. S. (Lori S.), Thibodeau, S. N. (Stephen N.), French, A. J. (Amy J.), Cerhan, J. R. (James R.), Wang, L.-D. (Li-Dong), Wei, G.-H. (Gong-Hong), Wang, L. (Liang)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::761d526f6fe5c53ee926c03c5329b8e1
http://urn.fi/urn:nbn:fi-fe2018081433653
http://urn.fi/urn:nbn:fi-fe2018081433653