A comparative evaluation of hybrid error correction methods for error-prone long reads.

Genome Biol

Department of Internal Medicine, University of Iowa, Iowa City, IA, 52242, USA.

Published: February 2019

Background: Third-generation sequencing technologies have advanced the progress of the biological research by generating reads that are substantially longer than second-generation sequencing technologies. However, their notorious high error rate impedes straightforward data analysis and limits their application. A handful of error correction methods for these error-prone long reads have been developed to date. The output data quality is very important for downstream analysis, whereas computing resources could limit the utility of some computing-intense tools. There is a lack of standardized assessments for these long-read error-correction methods.

Results: Here, we present a comparative performance assessment of ten state-of-the-art error-correction methods for long reads. We established a common set of benchmarks for performance assessment, including sensitivity, accuracy, output rate, alignment rate, output read length, run time, and memory usage, as well as the effects of error correction on two downstream applications of long reads: de novo assembly and resolving haplotype sequences.

Conclusions: Taking into account all of these metrics, we provide a suggestive guideline for method choice based on available data size, computing resources, and individual research goals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362602PMC
http://dx.doi.org/10.1186/s13059-018-1605-zDOI Listing

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