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PMID: 23155066 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

DiffSplice: the genome-wide detection of differential splicing events with RNA-seq.

Nucleic acids research ·Vol. 41 ·No. 2 ·2013-01-00 ·Pages e39

Hu Y, Huang Y, Du Y, Orellana CF, Singh D, Johnson AR, Monroy A, Kuan PF, Hammond SM, Makowski L, Randell SH, Chiang DY, Hayes DN, Jones C, Liu Y, Prins JF, Liu J

Abstract

The RNA transcriptome varies in response to cellular differentiation as well as environmental factors, and can be characterized by the diversity and abundance of transcript isoforms. Differential transcription analysis, the detection of differences between the transcriptomes of different cells, may improve understanding of cell differentiation and development and enable the identification of biomarkers that classify disease types. The availability of high-throughput short-read RNA sequencing technologies provides in-depth sampling of the transcriptome, making it possible to accurately detect the differences between transcriptomes. In this article, we present a new method for the detection and visualization of differential transcription. Our approach does not depend on transcript or gene annotations. It also circumvents the need for full transcript inference and quantification, which is a challenging problem because of short read lengths, as well as various sampling biases. Instead, our method takes a divide-and-conquer approach to localize the difference between transcriptomes in the form of alternative splicing modules (ASMs), where transcript isoforms diverge. Our approach starts with the identification of ASMs from the splice graph, constructed directly from the exons and introns predicted from RNA-seq read alignments. The abundance of alternative splicing isoforms residing in each ASM is estimated for each sample and is compared across sample groups. A non-parametric statistical test is applied to each ASM to detect significant differential transcription with a controlled false discovery rate. The sensitivity and specificity of the method have been assessed using simulated data sets and compared with other state-of-the-art approaches. Experimental validation using qRT-PCR confirmed a selected set of genes that are differentially expressed in a lung differentiation study and a breast cancer data set, demonstrating the utility of the approach applied on experimental biological data sets. The software of DiffSplice is available at http://www.netlab.uky.edu/p/bioinfo/DiffSplice.

MeSH Terms
Alternative Splicing Breast Neoplasms/genetics,metabolism Cell Differentiation Female Gene Expression Profiling Genome, Human Humans Lung/cytology,metabolism Sequence Analysis, RNA Software Transcriptome
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Hu Yin
Department of Computer Science, University of Kentucky, Lexington, KY 40506, USA.
Huang Yan
Du Ying
Orellana Christian F
Singh Darshan
Johnson Amy R
Monroy Anaïs
Kuan Pei-Fen
Hammond Scott M
Makowski Liza
Randell Scott H
Chiang Derek Y
Hayes D Neil
Jones Corbin
Liu Yufeng
Prins Jan F
Liu Jinze
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
1362-4962
Published
2013-01-00
Epub
2012-00-15
Pages
e39
Language
English
Region
England
NLM ID
0411011
PMCID
PMC3553996
Subset
IM
Grants
NCI NIH HHS · U24-CA143848 · United States
NCI NIH HHS · 3U24-CA143848-02S1 · United States
NCI NIH HHS · P30 CA016086 · United States
NIAAA NIH HHS · AA017376 · United States
NCI NIH HHS · R01-CA149569-03 · United States
NHLBI NIH HHS · RC1-HL100108 · United States
NHGRI NIH HHS · R01 HG006272 · United States
NHGRI NIH HHS · R01-HG006272 · United States
NCI NIH HHS · R01 CA149569 · United States
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