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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

Project Activity

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Categories

Bio-Informatics

License

MIT License, GNU General Public License version 3.0 (GPLv3)

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Additional Project Details

Operating Systems

Linux, BSD

Languages

English

Intended Audience

Science/Research

User Interface

Command-line

Programming Language

C

Related Categories

C Bio-Informatics Software

Registered

2009-09-01
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