Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel

被引：0
|
作者：
Mitt, Mario [1 ,2 ]
Kals, Mart [1 ,3 ]
Parn, Kalle [1 ,4 ]
Gabriel, Stacey B. [5 ]
Lander, Eric S. [5 ]
Palotie, Aarno [4 ,5 ]
Ripatti, Samuli [4 ]
Morris, Andrew P. [1 ,6 ]
Metspalu, Andres [1 ,2 ]
Esko, Tonu [1 ,5 ]
Magi, Reedik [1 ]
Palta, Priit [1 ,4 ]
机构：
[1] Univ Tartu, Estonian Genome Ctr, Tartu, Estonia
[2] Univ Tartu, Inst Mol & Cell Biol, Dept Biotechnol, Tartu, Estonia
[3] Univ Tartu, Inst Math & Stat, Tartu, Estonia
[4] Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki, Finland
[5] Broad Inst MIT & Harvard, Cambridge, MA USA
[6] Univ Liverpool, Dept Biostat, Liverpool, Merseyside, England
来源：
HUMAN HEREDITY | 2016年 / 81卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
P22
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收藏
页码：235 / 235
页数：1
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