Mercurial > repos > miller-lab > genome_diversity
diff calctfreq.py @ 12:4b6590dd7250
Uploaded
author | miller-lab |
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date | Wed, 12 Sep 2012 17:10:26 -0400 |
parents | 2c498d40ecde |
children | d6b961721037 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/calctfreq.py Wed Sep 12 17:10:26 2012 -0400 @@ -0,0 +1,114 @@ +#!/usr/bin/env python +# -*- coding: utf-8 -*- +# +# calcfreq.py +# +# Copyright 2011 Oscar Bedoya-Reina <oscar@niska.bx.psu.edu> +# +# This program is free software; you can redistribute it and/or modify +# it under the terms of the GNU General Public License as published by +# the Free Software Foundation; either version 2 of the License, or +# (at your option) any later version. +# +# This program is distributed in the hope that it will be useful, +# but WITHOUT ANY WARRANTY; without even the implied warranty of +# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the +# GNU General Public License for more details. +# +# You should have received a copy of the GNU General Public License +# along with this program; if not, write to the Free Software +# Foundation, Inc., 51 Franklin Street, Fifth Floor, Boston, +# MA 02110-1301, USA. + +import argparse,os,sys +from decimal import Decimal,getcontext +from LocationFile import LocationFile + +#method to rank the the pthways by mut. freq. +def rankd(ltfreqs): + ordvals=sorted(ltfreqs)#sort and reverse freqs. + #~ + outrnk=[] + tmpFreq0,tmpCount,tmpPthw=ordvals.pop()#the highest possible value + crank=1 + outrnk.append('\t'.join([str(tmpCount),str(tmpFreq0),str(crank),tmpPthw])) + totalnvals=len(ordvals) + cnt=0 + while totalnvals>cnt: + cnt+=1 + tmpFreq,tmpCount,tmpPthw=ordvals.pop() + if tmpFreq!=tmpFreq0: + crank=len(outrnk)+1 + tmpFreq0=tmpFreq + outrnk.append('\t'.join([str(tmpCount),str(tmpFreq),str(crank),tmpPthw])) + return outrnk + + +def main(): + parser = argparse.ArgumentParser(description='Obtain KEGG images from a list of genes.') + parser.add_argument('--input',metavar='input TXT file',type=str,help='the input file with the table in txt format') + parser.add_argument('--output',metavar='output TXT file',type=str,help='the output file with the table in txt format. Column 1 is the count of genes in the list, Column 2 is the percentage of the pathway genes present on the list. Column 3 is the rank based on column 2') + parser.add_argument('--posKEGGclmn',metavar='column number',type=int,help='the column with the KEGG pathway code/name') + parser.add_argument('--KEGGgeneposcolmn',metavar='column number',type=int,help='column with the KEGG gene code') + parser.add_argument('--loc_file',metavar='location file',type=str,help='location file') + parser.add_argument('--species',metavar='species',type=str,help='species') + #~Open arguments + class C(object): + pass + fulargs=C() + parser.parse_args(sys.argv[1:],namespace=fulargs) + #test input vars + inputf,outputf,posKEGGclmn,Kgeneposcolmn=fulargs.input,fulargs.output,fulargs.posKEGGclmn,fulargs.KEGGgeneposcolmn + locf,species=fulargs.loc_file,fulargs.species + #make a dictionary of valid genes + posKEGGclmn-=1 + Kgeneposcolmn-=1 + dKEGGcPthws=dict([(x.split('\t')[Kgeneposcolmn],set(x.split('\t')[posKEGGclmn].split('.'))) for x in open(inputf).read().splitlines()[1:] if x.strip()]) + sdGenes=set([x for x in dKEGGcPthws.keys() if x.find('.')>-1]) + while True:#to correct names with more than one gene + try: + mgenes=sdGenes.pop() + pthwsAssotd=dKEGGcPthws.pop(mgenes) + mgenes=mgenes.split('.') + for eachg in mgenes: + dKEGGcPthws[eachg]=pthwsAssotd + except: + break + #~ Count genes + getcontext().prec=2#set 2 decimal places + + location_file = LocationFile(locf) + prefix, kxml_dir_path, dict_file = location_file.get_values(species) + dPthContsTotls = {} + try: + with open(dict_file) as fh: + for line in fh: + line = line.rstrip('\r\n') + value, key = line.split('\t') + dPthContsTotls[key] = int(value) + except IOError, err: + print >> sys.stderr, 'Error opening dict file {0}: {1}'.format(dict_file, err.strerror) + sys.exit(1) + + dPthContsTmp=dict([(x,0) for x in dPthContsTotls.keys()])#create a list of genes + sdGenes=set([x for x in dKEGGcPthws.keys()])#list of all genes + cntGens=0 + ltGens=len(sdGenes) + while cntGens<ltGens: + cGen=sdGenes.pop() + sKEGGcPthws=dKEGGcPthws.pop(cGen) + for eachP in sKEGGcPthws: + if eachP!='N': + dPthContsTmp[eachP]+=1 + cntGens+=1 + #~ Calculate Freqs. + ltfreqs=[((Decimal(dPthContsTmp[x])/Decimal(dPthContsTotls[x])),Decimal(dPthContsTmp[x]),x) for x in dPthContsTotls] + tabllfreqs='\n'.join(rankd(ltfreqs)) + salef=open(outputf,'w') + salef.write(tabllfreqs) + salef.close() + return 0 + + +if __name__ == '__main__': + main()