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FMLRC: Hybrid long read error correction using an FM-index.

Jeremy R Wang1, James Holt2, Leonard McMillan2

  • 1Department of Genetics, University of North Carolina at Chapel Hill, CB 3280, 3144 Genome Sciences Building, 250 Bell Tower Dr, Chapel Hill, 27599, NC, USA. jeremy_wang@med.unc.edu.

BMC Bioinformatics
|February 11, 2018
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Summary
This summary is machine-generated.

This study introduces a novel hybrid method for correcting long read sequencing errors using short reads. The approach enhances genome assembly contiguity and throughput, making long read technologies more economically viable for complex genomes.

Keywords:
BWTFM-IndexHybrid error correctionLong readPacbiode novo assembly

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Long read sequencing offers improved genome assembly continuity and accuracy despite high error rates.
  • Current long read technologies face limitations in cost and throughput for complex genomes.
  • Hybrid assembly strategies, using long reads for scaffolding and short reads for accuracy, present a potential solution.

Purpose of the Study:

  • To develop and evaluate a novel hybrid method for correcting long read sequencing errors.
  • To improve the efficiency and accuracy of de novo genome assembly using long and short reads.
  • To enhance the economic viability of long read sequencing technologies.

Main Methods:

  • A novel method employing a multi-string Burrows-Wheeler Transform with an auxiliary FM-index was developed.
  • The method corrects errors in long reads by utilizing complementary short read data.
  • Performance was evaluated against existing hybrid error-correction and de novo assembly methods.

Main Results:

  • The novel method efficiently produces high-quality corrected long reads, surpassing existing hybrid approaches.
  • Resulting de novo assemblies exhibit significantly improved contiguity compared to state-of-the-art methods.
  • Increased throughput of corrected long reads was demonstrated.

Conclusions:

  • The developed method accurately corrects long read sequence data using short reads.
  • The approach leads to more contiguous de novo assemblies with higher throughput.
  • Improved computational efficiency and throughput make long read sequencing more economically accessible.