Skip to main content

Scrible: Ultra-Accurate Error-Correction of Pooled Sequenced Reads

  • Conference paper
  • First Online:
Book cover Algorithms in Bioinformatics (WABI 2015)

Part of the book series: Lecture Notes in Computer Science ((LNBI,volume 9289))

Included in the following conference series:

Abstract

We recently proposed a novel clone-by-clone protocol for de novo genome sequencing that leverages combinatorial pooling design to overcome the limitations of DNA barcoding when multiplexing a large number of samples on second-generation sequencing instruments. Here we address the problem of correcting the short reads obtained from our sequencing protocol. We introduce a novel algorithm called Scrible that exploits properties of the pooling design to accurately identify/correct sequencing errors and minimize the chance of “over-correcting”. Experimental results on synthetic data on the rice genome demonstrate that our method has much higher accuracy in correcting short reads compared to state-of-the-art error-correcting methods. On real data on the barley genome we show that Scrible significantly improves the decoding accuracy of short reads to individual BACs.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight 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

References

  1. Duma, D., et al.: Accurate decoding of pooled sequenced data using compressed sensing. In: Darling, A., Stoye, J. (eds.) WABI 2013. LNCS, vol. 8126, pp. 70–84. Springer, Heidelberg (2013)

    Chapter  Google Scholar 

  2. Earl, D., et al.: Assemblathon 1: a competitive assessment of de novo short read assembly methods. Genome Res. 21(12), 2224–2241 (2011)

    Article  Google Scholar 

  3. Engler, F., et al.: Locating sequence on FPC maps and selecting a minimal tiling path. Genome Res. 13(9), 2152–2163 (2003)

    Article  Google Scholar 

  4. Ilie, L., et al.: HiTEC: accurate error correction in high-throughput sequencing data. Bioinform. 27(3), 295–302 (2011)

    Article  Google Scholar 

  5. Ilie, L., Molnar, M.: RACER: rapid and accurate correction of errors in reads. Bioinform. 29(19), 2490–2493 (2013)

    Article  Google Scholar 

  6. Kelley, D.R., et al.: Quake: quality-aware detection and correction of sequencing errors. Genome Biol. 11(11), R116 (2010)

    Article  Google Scholar 

  7. Langmead, B., et al.: Ultrafast and memory-efficient alignment of short dna sequences to the human genome. Genome Biol. 10(3), R25 (2009)

    Article  Google Scholar 

  8. Lonardi, S., et al.: Combinatorial pooling enables selective sequencing of the barley gene space. PLoS Comput. Biol. 9(4), e1003010 (2013)

    Article  MathSciNet  Google Scholar 

  9. Lonardi, S., et al.: When less is more: "slicing" sequencing data improves read decoding accuracy and De Novo assembly quality. Bioinform. 31, 12 (2015). doi:10.1093/bioinformatics/btv311

    Article  Google Scholar 

  10. Mirebrahim, H., et al.: De Novo meta-assembly of ultra-deep sequencing data. Bioinform. 31(12), i9–i16 (2015)

    Article  Google Scholar 

  11. Russell, S., Norvig, P., et al.: Artificial Intelligence: A Modern Approach. Prentice-Hall Inc, Upper Saddle River, NJ, USA (1996). ch. 3

    MATH  Google Scholar 

  12. Salmela, L., Schroder, J.: Correcting errors in short reads by multiple alignments. Bioinform. 27(11), 1455–1461 (2011)

    Article  Google Scholar 

  13. Schroder, J., et al.: SHREC: a short-read error correction method. Bioinform. 25, 2157–2163 (2009)

    Article  Google Scholar 

  14. Simpson, J.T., Durbin, R.: Efficient de novo assembly of large genomes using compressed data structures. Genome Res. 22(3), 549–556 (2012)

    Article  Google Scholar 

  15. The International Barley Genome Sequencing Consortium: Nature. A physical, genetic and functional sequence assembly of the barley genome. 491(7426), 711–716 (2012)

    Google Scholar 

  16. Thierry-Mieg, N.: A new pooling strategy for high-throughput screening: the shifted transversal design. BMC Bioinform. 7, 28 (2006)

    Article  Google Scholar 

  17. Yang, X., et al.: Reptile: representative tiling for short read error correction. Bioinform. 26(20), 2526–2533 (2010)

    Article  Google Scholar 

  18. Zerbino, D., Birney, E.: Velvet: Algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 8(5), 821–829 (2008)

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Denise Duma .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2015 Springer-Verlag Berlin Heidelberg

About this paper

Cite this paper

Duma, D., Cordero, F., Beccuti, M., Ciardo, G., Close, T.J., Lonardi, S. (2015). Scrible: Ultra-Accurate Error-Correction of Pooled Sequenced Reads. In: Pop, M., Touzet, H. (eds) Algorithms in Bioinformatics. WABI 2015. Lecture Notes in Computer Science(), vol 9289. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-48221-6_12

Download citation

  • DOI: https://doi.org/10.1007/978-3-662-48221-6_12

  • Published:

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-48220-9

  • Online ISBN: 978-3-662-48221-6

  • eBook Packages: Computer ScienceComputer Science (R0)

Publish with us

Policies and ethics