The software developed is available in this page. This software will help guide the design of any study using RAD sequencing and related methods.
Download python and shell scritps
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pattern_for_genome.sh. This shell script will search all the restriction sites from the input file (patternfilename) in every genome from the input file (genomefilename). As a result this scripts creates
The input arguments are are:
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genomefilename: name of file with table with two columns (1) species code and (2) link to whole genome fasta file (see example/test_pattern_for_genome/example_genome_table )
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patternfilename - name of file with table with tow columns (1) restriction site regular expression and (2) restriction site name (see example/test_pattern_for_genome/patternfilename)
To run, just write on shell
patternforgenome.sh genomefilename patternfilename
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genome_nucleotide_distrib.py.
The input files are:
- genomefilename
- resultsfile
To run, just write on shell
python genomenucleotidedistrib.py genomefilename resultsfile
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sequence_probability.py
To run, just write on shell
python sequenceprobability.py distributionfile patternsfile