Next-generation sequencing approaches for genetic mapping of complex diseases

被引：13
|
作者：
Casals, Ferran [1 ,2 ]
Idaghdour, Youssef [1 ,2 ]
Hussin, Julie [1 ,3 ]
Awadalla, Philip [1 ,2 ]
机构：
[1] Univ Montreal, Ctr Rech, Ctr Hosp Univ St Justine, Montreal, PQ, Canada
[2] Univ Montreal, Dept Pediat, Fac Med, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Dept Biochim, Fac Med, Montreal, PQ H3C 3J7, Canada
来源：
JOURNAL OF NEUROIMMUNOLOGY | 2012年 / 248卷 / 1-2期
关键词：
Next-generation sequencing; Complex disease; Genomics; GENOME-WIDE ASSOCIATION; SINGLE-NUCLEOTIDE POLYMORPHISMS; AUTISM SPECTRUM DISORDERS; QUANTITATIVE-TRAIT LOCI; DE-NOVO MUTATIONS; MULTIPLE-SCLEROSIS; RARE VARIANTS; HIGH-THROUGHPUT; STRUCTURAL VARIATION; GENOTYPE IMPUTATION;
D O I：
10.1016/j.jneuroim.2011.12.017
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
The advent of next generation sequencing technologies has opened new possibilities in the analysis of human disease. In this review we present the main next-generation sequencing technologies, with their major contributions and possible applications to the study of the genetic etiology of complex diseases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码：10 / 22
页数：13
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