DynMap is an efficient, accurate, and sensitive tool for aligning short reads, obtained from next-generation sequencing, to multiple closely-related genomes. The programme can handle an enormous amount of single-end reads generated by the next-generation Illumina/Solexa Genome Analyzer.
Dr. Solon P. Pissis
- C Compiler
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Tomas Flouri, Costas S. Iliopoulos, and Solon P. Pissis.
DynMap : mapping short reads to multiple related genomes.
In Proceedings of the Second ACM International Conference on Bioinformatics and Computational Biology (ACM-BCB 2011), pp. 330-334, 2011. ACM Digital Library