Abstract
We present a new, accurate and efficient tool for mapping short reads obtained from the Illumina Genome Analyzer following sodium bisulfite conversion. Our tool, BRAT, supports single and paired-end reads and handles input files containing reads and mates of different lengths. BRAT is faster, maps more unique paired-end reads and has higher accuracy than existing programs. The software package includes tools to end-trim low-quality bases of the reads and to report nucleotide counts for mapped reads on the reference genome. Availability: The source code is freely available for download at http://compbio.cs.ucr.edu/brat/ and is distributed as Open Source software under the GPLv3.0. Contact: elenah@cs.ucr.edu Contact: elenah@cs.ucr.edu © The Author 2009. Published by Oxford University Press.
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CITATION STYLE
Harris, E. Y., Ponts, N., Levchuk, A., Le Roch, K., & Lonardi, S. (2009). BRAT: Bisulfite-treated reads analysis tool. Bioinformatics, 26(4), 572–573. https://doi.org/10.1093/bioinformatics/btp706
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