Skip to main content

Identification, Quantification, and Testing of Alternative Splicing Events from RNA-Seq Data Using SplAdder

  • Protocol
  • First Online:
Variant Calling

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2493))

  • 1750 Accesses

Abstract

Alternative splicing (AS) is a regulatory process during mRNA maturation that shapes higher eukaryotes’ complex transcriptomes. High-throughput sequencing of RNA (RNA-Seq) allows for measurements of AS transcripts at an unprecedented depth and diversity. The ever-expanding catalog of known AS events provides biological insights into gene regulation, population genetics, or in the context of disease. Here, we present an overview on the usage of SplAdder, a graph-based alternative splicing toolbox, which can integrate an arbitrarily large number of RNA-Seq alignments and a given annotation file to augment the shared annotation based on RNA-Seq evidence. The shared augmented annotation graph is then used to identify, quantify, and confirm alternative splicing events based on the RNA-Seq data. Splice graphs for individual alignments can also be tested for significant quantitative differences between other samples or groups of samples.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 249.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

Notes

  1. 1.

    http://www.ensembl.org/info/website/upload/gff.html.

References

  1. Wang ET, Sandberg R, Luo S et al (2008) Alternative isoform regulation in human tissue transcriptomes. Nature 456:470–476

    Article  CAS  Google Scholar 

  2. Pan Q, Shai O, Lee LJ et al (2008) Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat Genet 40:1413–1415

    Article  CAS  Google Scholar 

  3. Kahles A, Ong CS, Zhong Y, Rätsch G (2016) SplAdder: identification, quantification and testing of alternative splicing events from RNA-Seq data. Bioinformatics 32:1840–1847

    Article  CAS  Google Scholar 

  4. Dobin A, Davis CA, Schlesinger F et al (2013) STAR: ultrafast universal RNA-seq aligner. Bioinformatics 29:15–21

    CAS  PubMed  Google Scholar 

  5. Kim D, Paggi JM, Park C et al (2019) Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. Nat Biotechnol 37:907–915

    Article  CAS  Google Scholar 

  6. Frankish A, Diekhans M, Ferreira A-M et al (2019) GENCODE reference annotation for the human and mouse genomes. Nucleic Acids Res 47:D766–D773

    Article  CAS  Google Scholar 

  7. Yates AD, Achuthan P, Akanni W et al (2020) Ensembl 2020. Nucleic Acids Res 48:D682–D688

    Article  CAS  Google Scholar 

  8. Li H, Handsaker B, Wysoker A, Fennell T (2009) The sequence alignment/map format and SAMtools. Bioinformatics 25:2078–2079

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to André Kahles .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2022 The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Markolin, P., Rätsch, G., Kahles, A. (2022). Identification, Quantification, and Testing of Alternative Splicing Events from RNA-Seq Data Using SplAdder. In: Ng, C., Piscuoglio, S. (eds) Variant Calling. Methods in Molecular Biology, vol 2493. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2293-3_11

Download citation

  • DOI: https://doi.org/10.1007/978-1-0716-2293-3_11

  • Published:

  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-2292-6

  • Online ISBN: 978-1-0716-2293-3

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics