Annotation-free quantification of RNA splicing using LeafCutter

被引:392
作者
Li, Yang I. [1 ,6 ]
Knowles, David A. [1 ,2 ,3 ]
Humphrey, Jack [4 ,5 ]
Barbeira, Alvaro N. [6 ]
Dickinson, Scott P. [6 ]
Im, Hae Kyung [6 ]
Pritchard, Jonathan K. [1 ,7 ,8 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[4] UCL Genet Inst, Gower St, London, England
[5] UCL Inst Neurol, Dept Neurodegenerat Dis, London, England
[6] Univ Chicago, Dept Med, Sect Genet Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[7] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[8] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTOME; GENOME; ROBUST; EVOLUTION; MODEL; GENE;
D O I
10.1038/s41588-017-0004-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The excision of introns from pre-mRNA is an essential step in mRNA processing. We developed LeafCutter to study sample and population variation in intron splicing. LeafCutter identifies variable splicing events from short-read RNA-seq data and finds events of high complexity. Our approach obviates the need for transcript annotations and circumvents the challenges in estimating relative isoform or exon usage in complex splicing events. LeafCutter can be used both to detect differential splicing between sample groups and to map splicing quantitative trait loci (sQTLs). Compared with contemporary methods, our approach identified 1.4-2.1 times more sQTLs, many of which helped us ascribe molecular effects to disease-associated variants. Transcriptome-wide associations between LeafCutter intron quantifications and 40 complex traits increased the number of associated disease genes at a 5% false discovery rate by an average of 2.1-fold compared with that detected through the use of gene expression levels alone. LeafCutter is fast, scalable, easy to use, and available online.
引用
收藏
页码:151 / +
页数:9
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