Rapid and precise alignment of raw reads against redundant databases with KMA

Clausen PTLC, Aarestrup FM, Lund O

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Abstract

Background As the cost of sequencing has declined, clinical diagnostics based on next generation sequencing (NGS) have become reality. Diagnostics based on sequencing will require rapid and precise mapping against redundant databases because some of the most important determinants, such as antimicrobial resistance and core genome multilocus sequence typing (MLST) alleles, are highly similar to one another. In order to facilitate this, a novel mapping method, KMA (k-mer alignment), was designed. KMA is able to map raw reads directly against redundant databases, it also scales well for large redundant databases. KMA uses k-mer seeding to speed up mapping and the Needleman-Wunsch algorithm to accurately align extensions from k-mer seeds. Multi-mapping reads are resolved using a novel sorting scheme (ConClave scheme), ensuring an accurate selection of templates. Results The functionality of KMA was compared with SRST2, MGmapper, BWA-MEM, Bowtie2, Minimap2 and Salmon, using both simulated data and a dataset of Escherichia coli mapped against resistance genes and core genome MLST alleles. KMA outperforms current methods with respect to both accuracy and speed, while using a comparable amount of memory. Conclusion With KMA, it was possible map raw reads directly against redundant databases with high accuracy, speed and memory efficiency.

Abstract of "Rapid and precise alignment of raw reads against redundant databases with KMA" by Clausen PTLC, Aarestrup FM, Lund O, https://doi.org/10.1186/s12859-018-2336-6, used under its Creative Commons Attribution license (CC-BY); markup removed, otherwise unmodified.

Record

Archive ID
doi:10.1186/s12859-018-2336-6
Published
Aug 29, 2018
Venue
BMC bioinformatics
DOI
10.1186/s12859-018-2336-6
PubMed
30157759
PMC
PMC6116485
License
CC-BY
Provenance
europepmc

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