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

页码：10 / 22

页数：13

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