Population-specific genetic variation in large sequencing data sets: why more data is still better

被引:17
作者
van Rooij, Jeroen G. J. [1 ,2 ]
Jhamai, Mila [1 ]
Arp, Pascal P. [1 ]
Nouwens, Stephan C. A. [1 ]
Verkerk, Marijn [1 ]
Hofman, Albert [3 ,4 ]
Ikram, M. Arfan [2 ,3 ]
Verkerk, Annemieke J. [1 ]
van Meurs, Joyce B. J. [1 ]
Rivadeneira, Fernando [1 ]
Uitterlinden, Andre G. [1 ,2 ]
Kraaij, Robert [1 ]
机构
[1] Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
[2] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[3] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands
[4] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
关键词
D O I
10.1038/ejhg.2017.110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have generated a next-generation whole-exome sequencing data set of 2628 participants of the population-based Rotterdam Study cohort, comprising 669 737 single-nucleotide variants and 24 019 short insertions and deletions. Because of broad and deep longitudinal phenotyping of the Rotterdam Study, this data set permits extensive interpretation of genetic variants on a range of clinically relevant outcomes, and is accessible as a control data set. We show that next-generation sequencing data sets yield a large degree of population-specific variants, which are not captured by other available large sequencing efforts, being ExAC, ESP, 1000G, UK10K, GoNL and DECODE.
引用
收藏
页码:1173 / 1175
页数:3
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