Bioinformatics · 2019 · 1.3K citations · 12 references
Life SciencesBioinformaticsBiologyGenome AssemblyGenomicsSequence AnalysisDe Novo Genome AssemblyGenome SequencingLong-read AssemblyNext-generation SequencingSequence AssemblyShort-read AssemblyBase-level PolishingGenome PolishingK-mer-based PolishingLong-read PolishingShort-read Genome AssemblyShort-read Polishing
MOTIVATION: Although long-read sequencing technologies can produce genomes with long contiguity, they suffer from high error rates. Thus, we developed NextPolish, a tool that efficiently corrects sequence errors in genomes assembled with long reads. This new tool consists of two interlinked modules that are designed to score and count K-mers from high quality short reads, and to polish genome assemblies containing large numbers of base errors. RESULTS: When evaluated for the speed and efficiency using human and a plant (Arabidopsis thaliana) genomes, NextPolish outperformed Pilon by correcting sequence errors faster, and with a higher correction accuracy. AVAILABILITY AND IMPLEMENTATION: NextPolish is implemented in C and Python. The source code is available from https://github.com/Nextomics/NextPolish. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
12
Fast and accurate short read alignment with Burrows–Wheeler transform
Heng Li, Richard Durbin · Bioinformatics · 2009 · 62.8K citations · Full text
Minimap2: pairwise alignment for nucleotide sequences
Heng Li · Bioinformatics · 2018 · 16.8K citations · Full text
Bruce J. Walker, Thomas Abeel, Terrance Shea et al. · PLoS ONE · 2014 · 10.2K citations · Full text
HiC-Pro: an optimized and flexible pipeline for Hi-C data processing
Nicolas Servant, Nelle Varoquaux, Bryan R. Lajoie et al. · Genome biology · 2015 · 2.9K citations · Full text