Abstract
RNA sequencing (RNA-Seq) has emerged as a powerful and increasingly cost-effective technology for analysis of transcriptomes. RNA-Seq has several significant advantages over gene expression microarrays, including its high sensitivity and accuracy, broad dynamic range, nucleotide-level resolution, ability to detect novel mRNA transcripts, and ability to analyze pre-mRNA alternative splicing. A major application of RNA-Seq is to detect differential alternative splicing, i.e., differences in exon splicing patterns among different biological conditions. We recently developed a statistical method multivariate analysis of transcript splicing (MATS) for detecting differential alternative splicing events from RNA-Seq data. Here, we describe a computational pipeline RNASeq-MATS based on the MATS algorithm. This pipeline automatically detects and analyzes differential alternative splicing events corresponding to all major types of alternative splicing patterns from RNA-Seq data.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Wang ET, Sandberg R, Luo S, Khrebtukova I, Zhang L, Mayr C et al (2008) Alternative isoform regulation in human tissue transcriptomes. Nature 456(7221):470–476
Cooper TA, Wan L, Dreyfuss G (2009) RNA and disease. Cell 136(4):777–793
Wang Z, Gerstein M, Snyder M (2009) RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet 10(1):57–63
Griffith M, Griffith OL, Mwenifumbo J, Goya R, Morrissy AS, Morin RD et al (2010) Alternative expression analysis by RNA sequencing. Nat Methods 7(10):843–847
Katz Y, Wang ET, Airoldi EM, Burge CB (2010) Analysis and design of RNA sequencing experiments for identifying isoform regulation. Nat Methods 7(12):1009–1015
Brooks AN, Yang L, Duff MO, Hansen KD, Park JW, Dudoit S et al (2011) Conservation of an RNA regulatory map between Drosophila and mammals. Genome Res 21(2):193–202
Shen S, Park JW, Huang J, Dittmar KA, Lu ZX, Zhou Q et al (2012) MATS: a bayesian framework for flexible detection of differential alternative splicing from RNA-Seq data. Nucleic Acids Res 40(8):e61
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N et al (2009) The sequence alignment/map format and SAMtools. Bioinformatics 25(16):2078–2079
Langmead B, Trapnell C, Pop M, Salzberg SL (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10(3):R25
Trapnell C, Pachter L, Salzberg SL (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25(9):1105–1111
Trapnell C, Williams BA, Pertea G, Mortazavi A, Kwan G, van Baren MJ et al (2010) Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol 28(5):511–515
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media New York
About this protocol
Cite this protocol
Park, J.W., Tokheim, C., Shen, S., Xing, Y. (2013). Identifying Differential Alternative Splicing Events from RNA Sequencing Data Using RNASeq-MATS. In: Shomron, N. (eds) Deep Sequencing Data Analysis. Methods in Molecular Biology, vol 1038. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-514-9_10
Download citation
DOI: https://doi.org/10.1007/978-1-62703-514-9_10
Published:
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-1-62703-513-2
Online ISBN: 978-1-62703-514-9
eBook Packages: Springer Protocols