Mercurial > repos > xuebing > sharplabtool
view tools/rgenetics/rgPedSub.py @ 1:cdcb0ce84a1b
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author | xuebing |
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date | Fri, 09 Mar 2012 19:45:15 -0500 |
parents | 9071e359b9a3 |
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""" July 1 2009 added relatedness filter - fo/oo or all released under the terms of the LGPL copyright ross lazarus August 2007 for the rgenetics project Special galaxy tool for the camp2007 data Allows grabbing genotypes from an arbitrary region Needs a mongo results file in the location hardwired below or could be passed in as a library parameter - but this file must have a very specific structure rs chrom offset float1...floatn called as <command interpreter="python2.4"> campRGeno2.py $region "$rslist" "$title" $output1 $log_file $userId "$lpedIn" "$lhistIn" </command> """ import sys, array, os, string from rgutils import galhtmlprefix,plinke,readMap progname = os.path.split(sys.argv[0])[1] atrandic = {'A':'1','C':'2','G':'3','T':'4','N':'0','-':'0','1':'1','2':'2','3':'3','4':'4','0':'0'} def doImport(outfile='test',flist=[]): """ import into one of the new html composite data types for Rgenetics Dan Blankenberg with mods by Ross Lazarus October 2007 """ out = open(outfile,'w') out.write(galhtmlprefix % progname) if len(flist) > 0: out.write('<ol>\n') for i, data in enumerate( flist ): out.write('<li><a href="%s">%s</a></li>\n' % (os.path.split(data)[-1],os.path.split(data)[-1])) out.write('</ol>\n') else: out.write('No files found') out.write("</div></body></html>") out.close() def setupPedFilter(relfilter='oo',dfile=None): """ figure out who to drop to satisfy relative filtering note single offspring only from each family id ordering of pdict keys makes this 'random' as the first one only is kept if there are multiple sibs from same familyid. """ dropId = {} keepoff = (relfilter == 'oo') keepfounder = (relfilter == 'fo') pdict = {} for row in dfile: rowl = row.strip().split() if len(rowl) > 6: idk = (rowl[0],rowl[1]) pa = (rowl[0],rowl[2]) # key for father ma = (rowl[0],rowl[3]) # and mother pdict[idk] = (pa,ma) dfile.seek(0) # rewind pk = pdict.keys() for p in pk: parents = pdict[p] if pdict.get(parents[0],None) or pdict.get(parents[1],None): # parents are in this file if keepfounder: dropId[p] = 1 # flag for removal elif keepoff: dropId[p] = 1 # flag for removal if keepoff: # TODO keep only a random offspring if many - rely on pdict keys being randomly ordered...! famseen = {} for p in pk: # look for multiples from same family - drop all but first famid = p[0] if famseen.get(famid,None): dropId[p] = 1 # already got one from this family famseen.setdefault(famid,1) return dropId def writeFped(rslist=[],outdir=None,title='Title',basename='',dfile=None,wewant=[],dropId={},outfile=None,logfile=None): """ fbat format version """ outname = os.path.join(outdir,basename) pedfname = '%s.ped' % outname ofile = file(pedfname, 'w') rsl = ' '.join(rslist) # rslist for fbat ofile.write(rsl) s = 'wrote %d marker header to %s - %s\n' % (len(rslist),pedfname,rsl[:50]) lf.write(s) ofile.write('\n') nrows = 0 for line in dfile: line = line.strip() if not line: continue line = line.replace('D','N') fields = line.split() preamble = fields[:6] idk = (preamble[0],preamble[1]) dropme = dropId.get(idk,None) if not dropme: g = ['%s %s' % (fields[snpcol], fields[snpcol+1]) for snpcol in wewant] g = ' '.join(g) g = g.split() # we'll get there g = [atrandic.get(x,'0') for x in g] # numeric alleles... # hack for framingham ND ofile.write('%s %s\n' % (' '.join(preamble), ' '.join(g))) nrows += 1 ofile.close() loglist = open(logfile,'r').readlines() # retrieve log to add to html file doImport(outfile,[pedfname,],loglist=loglist) return nrows,pedfname def writePed(markers=[],outdir=None,title='Title',basename='',dfile=None,wewant=[],dropId={},outfile=None,logfile=None): """ split out """ outname = os.path.join(outdir,basename) mapfname = '%s.map' % outname pedfname = '%s.ped' % outname ofile = file(pedfname, 'w') # make a map file in the lped library mf = file(mapfname,'w') map = ['%s\t%s\t0\t%d' % (x[0],x[2],x[1]) for x in markers] # chrom,abspos,snp in genomic order mf.write('%s\n' % '\n'.join(map)) mf.close() nrows = 0 for line in dfile: line = line.strip() if not line: continue #line = line.replace('D','N') fields = line.split() preamble = fields[:6] idk = (preamble[0],preamble[1]) dropme = dropId.get(idk,None) if not dropme: g = ['%s %s' % (fields[snpcol], fields[snpcol+1]) for snpcol in wewant] g = ' '.join(g) g = g.split() # we'll get there g = [atrandic.get(x,'0') for x in g] # numeric alleles... # hack for framingham ND ofile.write('%s %s\n' % (' '.join(preamble), ' '.join(g))) nrows += 1 ofile.close() loglist = open(logfile,'r').readlines() # retrieve log to add to html file doImport(outfile,[mapfname,pedfname,logfile]) return nrows,pedfname def subset(): """ ### Sanity check the arguments now passed in as <command interpreter="python"> rgPedSub.py $script_file </command> with <configfiles> <configfile name="script_file"> title~~~~$title output1~~~~$output1 log_file~~~~$log_file userId~~~~$userId outformat~~~~$outformat outdir~~~~$output1.extra_files_path relfilter~~~~$relfilter #if $d.source=='library' inped~~~~$d.lpedIn #else inped~~~~$d.lhistIn.extra_files_path/$d.lhistIn.metadata.base_name #end if #if $m.mtype=='grslist' rslist~~~~$m.rslist region~~~~ #else rslist~~~~ region~~~~$m.region #end if </configfile> </configfiles> """ sep = '~~~~' # arbitrary choice conf = {} if len(sys.argv) < 2: print >> sys.stderr, "No configuration file passed as a parameter - cannot run" sys.exit(1) configf = sys.argv[1] config = file(configf,'r').readlines() for row in config: row = row.strip() if len(row) > 0: try: key,valu = row.split(sep) conf[key] = valu except: pass ss = '%s%s' % (string.punctuation,string.whitespace) ptran = string.maketrans(ss,'_'*len(ss)) ### Figure out what genomic region we are interested in region = conf.get('region','') orslist = conf.get('rslist','').replace('X',' ').lower() orslist = orslist.replace(',',' ').lower() # galaxy replaces newlines with XX - go figure title = conf.get('title','').translate(ptran) # for outputs outfile = conf.get('output1','') outdir = conf.get('outdir','') try: os.makedirs(outdir) except: pass outformat = conf.get('outformat','lped') basename = conf.get('basename',title) logfile = os.path.join(outdir,'%s.log' % title) userId = conf.get('userId','') # for library pedFileBase = conf.get('inped','') relfilter = conf.get('relfilter','') MAP_FILE = '%s.map' % pedFileBase DATA_FILE = '%s.ped' % pedFileBase title = conf.get('title','lped subset') lf = file(logfile,'w') lf.write('config file %s = \n' % configf) lf.write(''.join(config)) c = '' spos = epos = 0 rslist = [] rsdict = {} if region > '': try: # TODO make a regexp? c,rest = region.split(':') c = c.replace('chr','') rest = rest.replace(',','') # remove commas spos,epos = rest.split('-') spos = int(spos) epos = int(epos) s = '## %s parsing chrom %s from %d to %d\n' % (progname,c,spos,epos) lf.write(s) except: s = '##! %s unable to parse region %s - MUST look like "chr8:10,000-100,000\n' % (progname,region) lf.write(s) lf.close() sys.exit(1) else: rslist = orslist.split() # galaxy replaces newlines with XX - go figure rsdict = dict(zip(rslist,rslist)) allmarkers = False if len(rslist) == 0 and epos == 0: # must be a full extract - presumably remove relateds or something allmarkers = True ### Figure out which markers are in this region markers,snpcols,rslist,rsdict = readMap(mapfile=MAP_FILE,allmarkers=allmarkers,rsdict=rsdict,c=c,spos=spos,epos=epos) if len(rslist) == 0: s = '##! %s found no rs numbers in %s\n' % (progname,sys.argv[1:3]) lf.write(s) lf.write('\n') lf.close() sys.exit(1) s = '## %s looking for %d rs (%s....etc)\n' % (progname,len(rslist),rslist[:5]) lf.write(s) try: dfile = open(DATA_FILE, 'r') except: # bad input file name? s = '##! rgPedSub unable to open file %s\n' % (DATA_FILE) lf.write(s) lf.write('\n') lf.close() print >> sys.stdout, s raise sys.exit(1) if relfilter <> 'all': # must read pedigree and figure out who to drop dropId = setupPedFilter(relfilter=relfilter,dfile=dfile) else: dropId = {} wewant = [(6+(2*snpcols[x])) for x in rslist] # # column indices of first geno of each marker pair to get the markers into genomic ### ... and then parse the rest of the ped file to pull out ### the genotypes for all subjects for those markers # /usr/local/galaxy/data/rg/1/lped/ if len(dropId.keys()) > 0: s = '## dropped the following subjects to satisfy requirement that relfilter = %s\n' % relfilter lf.write(s) if relfilter == 'oo': s = '## note that one random offspring from each family was kept if there were multiple offspring\n' lf.write(s) s = 'FamilyId\tSubjectId\n' lf.write(s) dk = dropId.keys() dk.sort() for k in dk: s = '%s\t%s\n' % (k[0],k[1]) lf.write(s) lf.write('\n') lf.close() if outformat == 'lped': nrows,pedfname=writePed(markers=markers,outdir=outdir,title=title,basename=basename,dfile=dfile, wewant=wewant,dropId=dropId,outfile=outfile,logfile=logfile) elif outformat == 'fped': nrows,pedfname=writeFped(rslist=rslist,outdir=outdir,title=title,basename=basename,dfile=dfile, wewant=wewant,dropId=dropId,outfile=outfile,logfile=logfile) dfile.close() if __name__ == "__main__": subset()