| Literature DB >> 22084252 |
Francesco Vezzi1, Cristian Del Fabbro, Alexandru I Tomescu, Alberto Policriti.
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.Entities:
Mesh:
Year: 2011 PMID: 22084252 DOI: 10.1093/bioinformatics/btr617
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937