Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hong Wen"'
Rare variant association analysis in case-parents studies by allowing for missing parental genotypes
Publikováno v:
BMC Genetics
BMC Genetics, Vol 19, Iss 1, Pp 1-8 (2018)
BMC Genetics, Vol 19, Iss 1, Pp 1-8 (2018)
Background The development of next-generation sequencing technologies has facilitated the identification of rare variants. Family-based design is commonly used to effectively control for population admixture and substructure, which is more prominent
Autor:
Ji-Rong, Long, Lan-Juan, Zhao, Peng-Yuan, Liu, Yan, Lu, Volodymyr, Dvornyk, Hui, Shen, Yong-Jun, Liu, Yuan-Yuan, Zhang, Dong-Hai, Xiong, Peng, Xiao, Hong-Wen, Deng
Publikováno v:
BMC Genetics, Vol 5, Iss 1, p 11 (2004)
BMC Genetics
BMC Genetics
Background The adequacy of association studies for complex diseases depends critically on the existence of linkage disequilibrium (LD) between functional alleles and surrounding SNP markers. Results We examined the patterns of LD and haplotype distri
Autor:
Hong-Wen Deng, Peng Xiao, Robert R. Recker, Yong Jun Liu, Hui Shen, Sonia M. Rocha-Sanchez, Lan Juan Zhao, Yuan Yuan Zhang, Jirong Long, Volodymyr Dvornyk, Dong Hai Xiong, Pengyuan Liu
Publikováno v:
BMC Genetics. 5:4
Public SNP databases are frequently used to choose SNPs for candidate genes in the association and linkage studies of complex disorders. However, their utility for such studies of diseases with ethnic-dependent background has never been evaluated. To
Autor:
Dvornyk, Volodymyr, Ji-Rong Long, Dong-Hai Xiong, Peng-Yuan Liu, Lan-Juan Zhao, Hui Shen, Yuan-Yuan Zhang, Yong-Jun Liu, Rocha-Sanchez, Sonia, Peng Xiao, Recker, Robert R., Hong-Wen Deng
Publikováno v:
BMC Genetics; 2004, Vol. 5, p4-15, 15p, 7 Charts, 2 Graphs
Autor:
Shen Hui, Dvornyk Volodymyr, Lu Yan, Liu Peng-Yuan, Zhao Lan-Juan, Long Ji-Rong, Liu Yong-Jun, Zhang Yuan-Yuan, Xiong Dong-Hai, Xiao Peng, Deng Hong-Wen
Publikováno v:
BMC Genetics, Vol 5, Iss 1, p 11 (2004)
Abstract Background The adequacy of association studies for complex diseases depends critically on the existence of linkage disequilibrium (LD) between functional alleles and surrounding SNP markers. Results We examined the patterns of LD and haploty
Externí odkaz:
https://doaj.org/article/e1bf999eb277476a9ed9cd99e0715af0
Autor:
Xiao Peng, Rocha-Sanchez Sonia, Liu Yong-Jun, Zhang Yuan-Yuan, Shen Hui, Zhao Lan-Juan, Liu Peng-Yuan, Xiong Dong-Hai, Long Ji-Rong, Dvornyk Volodymyr, Recker Robert R, Deng Hong-Wen
Publikováno v:
BMC Genetics, Vol 5, Iss 1, p 4 (2004)
Abstract Background Public SNP databases are frequently used to choose SNPs for candidate genes in the association and linkage studies of complex disorders. However, their utility for such studies of diseases with ethnic-dependent background has neve
Externí odkaz:
https://doaj.org/article/f1d0acb19e3d42ee91e954168532189e
Autor:
Long JR; Osteoporosis Research Center, Creighton University, Omaha, NE 68131, USA. jrlongyou@creighton.edu, Zhao LJ, Liu PY, Lu Y, Dvornyk V, Shen H, Liu YJ, Zhang YY, Xiong DH, Xiao P, Deng HW
Publikováno v:
BMC genetics [BMC Genet] 2004 May 24; Vol. 5, pp. 11. Date of Electronic Publication: 2004 May 24.