rNA: a fast and accurate short reads numerical aligner.
basic_science · Level V
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- Record sourced from PubMed, PMID 22084252.
- Also identified by DOI 10.1093/bioinformatics/btr617.
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Abstract
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/. vezzi@appliedgenomics.org; delfabbro@appliedgenomics.org Supplementary data are available at Bioinformatics online.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Sequence Alignment
- Sequence Analysis, DNA
- Software