BMC Bioinformatics (Nov 2012)

Improved base-calling and quality scores for 454 sequencing based on a Hurdle Poisson model

  • Beuf Kristof,
  • Schrijver Joachim,
  • Thas Olivier,
  • Criekinge Wim,
  • Irizarry Rafael A,
  • Clement Lieven

DOI
https://doi.org/10.1186/1471-2105-13-303
Journal volume & issue
Vol. 13, no. 1
p. 303

Abstract

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Abstract Background 454 pyrosequencing is a commonly used massively parallel DNA sequencing technology with a wide variety of application fields such as epigenetics, metagenomics and transcriptomics. A well-known problem of this platform is its sensitivity to base-calling insertion and deletion errors, particularly in the presence of long homopolymers. In addition, the base-call quality scores are not informative with respect to whether an insertion or a deletion error is more likely. Surprisingly, not much effort has been devoted to the development of improved base-calling methods and more intuitive quality scores for this platform. Results We present HPCall, a 454 base-calling method based on a weighted Hurdle Poisson model. HPCall uses a probabilistic framework to call the homopolymer lengths in the sequence by modeling well-known 454 noise predictors. Base-calling quality is assessed based on estimated probabilities for each homopolymer length, which are easily transformed to useful quality scores. Conclusions Using a reference data set of the Escherichia coli K-12 strain, we show that HPCall produces superior quality scores that are very informative towards possible insertion and deletion errors, while maintaining a base-calling accuracy that is better than the current one. Given the generality of the framework, HPCall has the potential to also adapt to other homopolymer-sensitive sequencing technologies.