Clustering of mRNA-Seq data based on alternative splicing patterns

被引:4
|
作者
Johnson, Marla [1 ]
Purdom, Elizabeth [2 ]
机构
[1] Univ Calif Berkeley, Div Biostat, 367 Evans Hall Berkeley, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Stat, 367 Evans Hall Berkeley, Berkeley, CA 94720 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Alternative splicing; Clustering; mRNA-Seq; ISOFORM EXPRESSION; SF3B1; MUTATIONS; MACHINERY; PATHWAY;
D O I
10.1093/biostatistics/kxw044
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sequencing of messenger RNA (mRNA) can provide estimates of the levels of individual isoforms within the cell. It remains to adapt many standard statistical methods commonly used for analyzing gene expression levels to take advantage of this additional information. One novel question is whether we can find clusters of samples that are distinguished not by their gene expression but by their isoform usage. We propose a novel approach for clustering mRNA-Seq data that identifies such clusters. We show via simulation that our methods are more sensitive to finding clusters based on isoform usage than standard clustering techniques. We demonstrate its performance by finding a technical artifact that resulted in different batches having different isoform usage patterns, and illustrate its usage on several The Cancer Genome Atlas datasets.
引用
收藏
页码:295 / 307
页数:13
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