Utilizing RNA-Seq data for de novo coexpression network inference

被引:134
作者
Iancu, Ovidiu D. [1 ]
Kawane, Sunita [2 ]
Bottomly, Daniel [2 ]
Searles, Robert
Hitzemann, Robert [1 ,3 ]
McWeeney, Shannon [2 ,4 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Oregon Clin & Translat Res Inst, Portland, OR 97239 USA
[3] Vet Affairs Med Ctr, Res Serv, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Dept Biostat Publ Hlth & Preventat Med, Portland, OR 97239 USA
关键词
GENE-EXPRESSION; ORGANIZATION; PACKAGE; TOOL;
D O I
10.1093/bioinformatics/bts245
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Motivation: RNA-Seq experiments have shown great potential for transcriptome profiling. While sequencing increases the level of biological detail, integrative data analysis is also important. One avenue is the construction of coexpression networks. Because the capacity of RNA-Seq data for network construction has not been previously evaluated, we constructed a coexpression network using striatal samples, derived its network properties and compared it with microarray-based networks. Results: The RNA-Seq coexpression network displayed scale-free, hierarchical network structure. We detected transcripts groups (modules) with correlated profiles; modules overlap distinct ontology categories. Neuroanatomical data from the Allen Brain Atlas reveal several modules with spatial colocalization. The network was compared with microarray-derived networks; correlations from RNA-Seq data were higher, likely because greater sensitivity and dynamic range. Higher correlations result in higher network connectivity, heterogeneity and centrality. For transcripts present across platforms, network structure appeared largely preserved. From this study, we present the first RNA-Seq data de novo network inference.
引用
收藏
页码:1592 / 1597
页数:6
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