Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jim Eberle"'
Autor:
Eunice Prakash, Andrew Boudreau, Ronald W. Davis, Tiffany Brundage, Hywel B. Jones, Paul Hardenbol, Maneesh Jain, Oleg Iartchouk, Fuli Yu, Ron Fitzgerald, Xin Miao, Sy Ghose, Richard A. Gibbs, Eugeni Namsaraev, Xiuhua Lu, George Karlin-Neumann, Karen Tran, Ayca Erbilgin, Carsten Bruckner, Zhiyong Wang, Jim Eberle, Steve Chow, Jennifer MacKenzie, Bridget Moore, Martin Moorhead, Mat Falkowski, John W. Belmont, Shiran Pasternak, Thomas D. Willis
Publikováno v:
Genome research. 15(2)
Complex human diseases are known to have a significant genetic component. Despite some important successes (Altshuler et al. 2000; Hugot et al. 2001), the elucidation of the underlying genetic determinants have proven resistant to standard methods. L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc8bfacfe00740ef728f5ebdbd8af9bd
https://pubmed.ncbi.nlm.nih.gov/15687290
https://pubmed.ncbi.nlm.nih.gov/15687290
Autor:
Thomas D. Willis, Ronald W. Davis, Kee Wong, Jim Eberle, Malek Faham, Eugeni Namsaraev, Jianbiao Zheng, Martin Moorhead, Yvonne R. Thorstenson, Hossein Fakhrai-Rad, Kent Suyenaga, Ted Jones
Publikováno v:
Genome research. 14(7)
A targeted discovery effort is required to identify low frequency single nucleotide polymorphisms (SNPs) in human coding and regulatory regions. We here describe combining mismatch repair detection (MRD) with dideoxy terminator sequencing to detect S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36cc21abb4baf1981c1d43998953e0c
https://pubmed.ncbi.nlm.nih.gov/15231755
https://pubmed.ncbi.nlm.nih.gov/15231755