BWA is a program for aligning sequencing reads against a large reference genome (e.g. human genome). It has two major components, one for read shorter than 150bp and the other for longer reads.
Features
- Support Illumina, SOLiD, 454, Sanger reads, PacBio reads and assembly contigs
- Gapped alignment and paired-end mapping
- Accurate, fast and lightweight
Categories
Bio-InformaticsLicense
MIT License, GNU General Public License version 3.0 (GPLv3)Follow Burrows-Wheeler Aligner
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