bowtie
Overview
Bowtie is an ultrafast, memory-efficient short read aligner geared toward quickly aligning large sets of short DNA sequences (reads) to large genomes.
Version 0.12.9 & 1.0.0 binaries are available on the iCSF.
Restrictions on use
All users may access and use Bowtie. The software is open source. Users should consult the following file for further information: $BOWTIE_HOME/$BOWTIE_VER/COPYING
For citation information see the Bowtie website.
Set up procedure
To use the software you will need to load the modulefile:
module load apps/binapps/bowtie/1.0.0
module load apps/binapps/bowtie/0.12.9
Indexes – No pre-built indexes have been installed. Users should download and build their own indexes and set the variable BOWTIE_INDEXES on the command line or in .bashrc . For example, in your scratch area:
export BOWTIE_INDEXES=$HOME/scratch/my_indexes
Running the application
Examples
- Build the
AF293
reference into the build formatcontig1.build
bowtie-build AF293_REF.fasta contig1.build
- Run bowtie to build a file of reads that don’t map to contig1 (
AF293
):bowtie -S -q contig1.build C023MABXX_3_5_1.fastq 351.sam --un unmapped351.fastq