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Detalle de: Acceleration of short and long DNA read mapping without loss of accuracy using suffix array

Title Acceleration of short and long DNA read mapping without loss of accuracy using suffix array
Abstract

HPG Aligner applies suffix arrays for DNA read mapping. This implementation produces a highly sensitive and extremely fast mapping of DNA reads that scales up almost linearly with read length. The approach presented here is faster (over 20× for long reads) and more sensitive (over 98% in a wide range of read lengths) than the current state-of-the-art mappers. HPG Aligner is not only an optimal alternative for current sequencers but also the only solution available to cope with longer reads and growing throughputs produced by forthcoming sequencing technologies. Availability and implementation: https://github.com/opencb/hpg-aligner. Contact: jdopazo@cipf.es or imedina@ebi.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.

Apa Reference Tárraga, J., Arnau, V., Martínez, H., Moreno, R., Cazorla, D., Salavert-Torres, J., Blanquer-Espert, I., Dopazo, J. & Medina, I. (2014). Acceleration of short and long DNA read mapping without loss of accuracy using suffix array. Bioinformatics, 30(23), 3396-3398. 10.1093/bioinformatics/btu553
Doi 10.1093/bioinformatics/btu553
Publication Date 20 Aug 2014
Publication Type Article
Researcher Vicente Arnau Lombart
Ontology Sequence Alignment, Mapping, Long-read sequencing
Research Groups
Tools

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