rNA: a fast and accurate short reads numerical aligner

Bioinformatics. 2012 Jan 1;28(1):123-4. doi: 10.1093/bioinformatics/btr617. Epub 2011 Nov 13.

Abstract

Summary: The advent of high-throughput sequencers (HTS) introduced the need of new tools in order to analyse the large amount of data that those machines are able to produce. The mandatory first step for a wide range of analyses is the alignment of the sequences against a reference genome. We present a major update to our rNA (randomized Numerical Aligner) tool. The main feature of rNA is the fact that it achieves an accuracy greater than the majority of other tools in a feasible amount of time. rNA executables and source codes are freely downloadable at http://iga-rna.sourceforge.net/.

Contact: vezzi@appliedgenomics.org; delfabbro@appliedgenomics.org

Supplementary information: Supplementary data are available at Bioinformatics online.

MeSH terms

  • High-Throughput Nucleotide Sequencing / methods*
  • Humans
  • Sequence Alignment / methods*
  • Sequence Analysis, DNA / methods*
  • Software*