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breseq

breseq is a computational pipeline for finding mutations relative to a reference sequence in short-read DNA re-sequencing data for haploid microbial-sized genomes. breseq is a command line tool implemented in C++ and R. It will compile and function on a variety of Unix platforms, including MacOSX and Cygwin. It reports single-nucleotide mutations, point insertions and deletions, large deletions, and new junctions supported by mosaic reads (such as those produced by new mobile element insertions) in an annotated HTML format.

Latest version from GitHub

Previous Versions:

Previous versions from 0.24rc6 to 0.25d (barricklab.org)

Previous versions up to 0.24rc6 (Google Code)

FASTQ reads for E. coli strain REL8593A (200M)

Reference genome (REL606)

Example of breseq output

Feedback and Bug Reporting

Please report bugs on GitHub.

Tutorial input and results files for breseq book chapter

Deatherage, D.E., Barrick, J.E.. (2014) Identification of mutations in laboratory-evolved microbes from next-generation sequencing data using breseq. Methods Mol. Biol. 1151:165-188. «PubMed»

Download Link	Size	Description
Clonal_Sample.tgz	267M	Input files for clonal sample
Clonal_Output.tgz	1.2M	Output files for clonal sample
Population_Sample.tgz	1.4G	Input files for time-course of population samples
Population_Output.tgz	11M	Output files for time-course of population samples, including comparison
Mutation_Examples.tgz	199K	Examples of using unassigned evidence to predict complex mutations
Poor_Evidence_Examples.tgz	139K	Example output showing characteristics of poor evidence