Description
The Subread package is developed in The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia. It consists of a suite of programs for processing next-gen sequencing data.
Home Page
http://bioinf.wehi.edu.au/subread-package/
Documentation
http://bioinf.wehi.edu.au/subread-package/SubreadUsersGuide.pdf
License
subread is free to use under GNU General Public License version 3.0 (GPLv3).
Usage
Use
module avail subread
to see which versions of subread are available. Use
module load subread/version
Build an index for the reference genome (you may provide a single FASTA file including all the reference sequences):
subread-buildindex -o my_index chr1.fa chr2.fa ...
Map single-end reads using 5 threads:
subread-align -T 5 -i my_index -r reads.txt -o subread_results.sam
Detect indels of up to 16bp:
subread-align -I 16 -i my_index -r reads.txt -o subread_results.sam
Report up to three best mapping locations:
subread-align -B 3 -i my_index -r reads.txt -o subread_results.sam
Report uniquely mapped reads only:
subread-align -u -i my_index -r reads.txt -o subread_results.sam
Map paired-end reads:
subread-align -d 50 -D 600 -i my_index -r reads1.txt -R reads2.txt -o subread_results_PE.samDetect fusions in genomic DNA sequencing data:
subread-align --reportFusions -d 50 -D 600 -i my_index -r reads1.txt -R reads2.txt -o subread_results.sam
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