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royshtsccodes061217.py
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royshtsccodes061217.py
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from __future__ import division
import re, sys, math, operator, copy,collections
import numpy as np
from itertools import groupby
def ProcessCLI(args):
pbi,scaf=readgff(args[1])
htscd=createHTSC(args[2],pbi)
htsc=[]
for s1 in htscd.keys():
LL=[]
for s2 in htscd[s1].keys():
#print s1,s2, len(htscd[s1][s2])
LL+=[htscd[s1][s2]]
htsc+=[LL]
#print LL
fillht(htsc,args[2],pbi)
return
# bestHits= readpsl(args[2],scaf_pb)
#for k in bestHits:
# print ' \t'.join([str(i) for i in list(k)])
def getInt(pb):
return [int(i) for i in re.split(r'(\d+)',pb) if len(i) >0 and i.isdigit()][0]
def getdup1(lst):
d={}
for key, value in lst:
d[key] = d.get(key, []) + [value]
for k in d:
if len(d[k])==1:
print k, ','.join(d[k])
else:
print 'dup:', k, '-->', ' '.join(d[k])
#return pdup(d)
def domainsplit_tandemdup_ohno(htscList,en_psl,gff):#if a single protein is hit by multiple other proteins when we compare pairs
#of scaffolds, we infer that there is a tandem duplication, or a domain splitting of one large protein, and choose a single
#best mate to form the ohnologan
bestmultL=[]
noscorebestmultL=[]
casesL=[]
for htsc in htscList:
doubles0=[]; doubles1=[]; mult={}
for tup in htsc:
if tup[0] not in doubles0:
doubles0+=[tup[0]]
else:
mult.add(tup[0])
if tup[1] not in doubles1:
doubles1+=[tup[1]]
else:
mult.add(tup[1])
for tup in htsc:
if tup[0] in mult:
if tup[0] not in doublesD.keys():
doublesD[tup[0]]=set()
else:
doublesD[tup[0]].add(tup[1])
else:
continue
if tup[1] in mult:
if tup[1] not in doublesD.keys():
doublesD[tup[1]]=set()
else:
doublesD[tup[1]].add(tup[0])
else:
continue
for k in doublesD.keys():
klen=0
vlentot=0
with open(gff,'r') as gfile:
for line in gfile:
if k in re.split('\W+',line[8]):
klen+=float((math.fabs(line[4] - line[3])))
for v in doublesD[k]:
if v in re.split('\W+',line[8]):
vlentot+=float((math.fabs(line[4] - line[3])))
if klen/vlentot > 1.5:
casesL+=[(k,doublesD[k],"tandem duplication")]
else:
casesL+=[(k,doublesD[k]),"domain split"]
#dummy=[]
with open(en_psl,'r') as psl:
for line in psl:
if ((line[0] == k and line[2] in doublesD[k]) or (line[0] in doublesD[k] and line[2]==k)) and line[1]!=line[3]:
bestmultL.append((line[0],line[2],(float(line[-3]),float(line[-2]))))#we now have a tuple with the ohnologan, & its bitscore&ev
noscorebestmultL.append((line[0],line[2]))
#bestmultL+=bestdoubles; #noscorebestmultL+=
return bestmultL, noscorebestmultL, casesL
##################################################################################################
#what we need to do now:
#1) the items in bestmultL are (p1, p2, (bscore,escore)) triples
#so, let's make 2-part tuples: for t in bmL: twomultL.append((t{0], t[1]))
#then: for htsc in htscList:
#build a list of mults
#for t in htsc:
#if t has a mult and t not in bmL and (t[1], t[0]) not in bmL:
#delete the tuple from htsc---it was a tandem duplication or a split domain, so that isn't an ohnolog
#if we need to know which was the case, we also have a list somewhere saying that (t[0], t[1], t[2]) was one of those cases
#where t[0] is 1 protein,t[1] is the set of other proteins in the gff that it hits, and t[2] is a string indicated which case
def remove_ds_td_extras(htscList, nsbmL):#see comments above
singly=htscList.copy()
for htsc in singly:
doubles0=[]; doubles1=[]; mult={}
for tup in htsc:
if tup[0] not in doubles0:
doubles0+=[tup[0]]
else:
mult.add(tup[0])
if tup[1] not in doubles1:
doubles1+=[tup[1]]
else:
mult.add(tup[0])
for tup in htsc:
for p in tup:
if p in mult:
if tup or (tup[1],tup[0]) in nsbmL:
continue
else:
#################################################
#DELETE THE TUPLE FROM THE htsc!!!!!!!!!!!!!!!!!!!!!!!!!
#But will this f**k up the indexing by which the for loop works? I hope not
#we will have to delete by value, not by index, that is for sure
#maybe use:
htsc.remove(tup)
return singly
def fillht(htscL, en_pslout_file,pbi):#infer synteny if hits between pairs of scaffolds are uniformly decreasing
#or uniformly increasing; if there are gaps in the synteny find appropriate hits that fill the holes and mark the pairs as
#ohnologans
'''now Roy must make copy of htscL and add the filled holes directly to it'''
holesList=[];l2hL=[];l2thhL=[];twohitsholesList=[]
hole1way=[]
newhtscList=[q for q in htscL]
for LT in newhtscList:
for htsc in LT:
newhits=set()
if len(htsc)>2:
print htsc[0]
return
for i in range(1,len(htsc)-1):
if getInt(htsc[i-1][0])< getInt(htsc[i][0]) and getInt(htsc[i][0])< getInt(htsc[i+1][0]):
if getInt(htsc[i-1][1])< getInt(htsc[i][1]) and getInt(htsc[i][1])< getInt(htsc[i+1][1]):
if getInt(htsc[i-1][0])<(getInt(htsc[i][0])-1) and getInt(htsc[i-1][1])<(getInt(htsc[i][1])-1):#if there is a hole on BOTH scafs
#there was a gap on the scaffold. now we want to fill it in.
'''if getInt(htsc[i-1][0])-(getInt(htsc[i][0])-1) == getInt(htsc[i-1][1])-getInt(htsc[i][1]):
#if the gaps are the same length on both scaffolds, we try to fill in the holes one at a time
for index,protein_int in enumerate(range((getInt(htsc[i-1][0])+1),getInt(htsc[i][0]))):
for line in en_pslout:
line=line.rstrip().split()
if (getInt(line[0]==protein_int) and getInt(line[2])==(getInt(htsc[i-1][1])+(index+1))\#if the pair exists at all in the
or getInt(line[2]==protein_int) and getInt(line[0])==(getInt(htsc[i-1][1])+(index+1))):#enriched psl output
##ADD THAT PAIR TO THE LIST OF OHNOLOGANS
##BUT IT DON'T KNOW WHAT THAT LIST IS CALLED---HELP ME, ETIENNE
elif getInt(htsc[i-1][0])-(getInt(htsc[i][0])-1) != getInt(htsc[i-1][1])-getInt(htsc[i][1]):'''
indivcol1=set(range(getInt(htsc[i-1][0])+1),getInt(htsc[i][0]))
indivcol2=set(range(getInt(htsc[i-1][1])+1),getInt(htsc[i][1]))
mycol=indivcol1.union(indivcol2)
dummy=[]
with open(en_pslout_file,'r') as en_pslout:
for line in en_pslout:
line=line.rstrp().split()
if getInt(line[0]) in mycol and getInt(line[1]) in mycol and pbi[line[0]]!=pbi[line[1]]:
dummy.append((line[0],line[1],(float(line[-3]),float(line[-2]))))#we now have a tuple with the ohnologan, & its bitscore&ev
dummy_s=sorted(dummy,key=lambda tup:(tup[2][0]),reverse=True)
allowed=set()#this code makes sure that we don't keep duplicates of a reciprocal hit
kill_it=[]
for tup in dummy_s:
if tup[0] not in allowed or tup[1] not in allowed:
allowed.add(tup[0]);allowed.add(tup[1])
else:
kill_it.append(tup)
for tupk in kill_it:
dummy_s.remove(tupk)
#dummy_top=dummy_s[0:(max(len(indivcol1),len(indivcol2))+1)]
length2=[(trip[0],trip[1]) for trip in dummy_s]
'''for trip in dummy_top:
length2.append((trip[0],trip[1]))'''
l2hL+=[length2]
newhits.add(length2)
holesList+=[dummy_top]
elif getInt(htsc[i-1][1])> getInt(htsc[i][1]) and getInt(htsc[i][1])> getInt(htsc[i+1][1]):#case: scafs in reverse order
if getInt(htsc[i-1][0])<(getInt(htsc[i][0])-1) and getInt(htsc[i-1][1])>(getInt(htsc[i][1])+1):#if there is a hole on BOTH scafs
indivcol1=set(range(getInt(htsc[i-1][0])+1),getInt(htsc[i][0]))
indivcol2=set(range(getInt(htsc[i-1][1])-1),getInt(htsc[i][1]),-1)
mycol=indivcol1.union(indivcol2)
dummy=[]
with open(en_pslout_file,'r') as en_pslout:
for line in en_pslout:
if getInt(line[0]) in mycol and getInt(line[1]) in mycol and pbi[line[0]]!=pbi[line[1]]:
dummy.append((line[0],line[1],(float(line[-3]),float(line[-2]))))#we now have a tuple with the ohnologan, & its bitscore&ev
dummy_s=sorted(dummy,key=lambda tup:(tup[2][0]),reverse=True)
allowed=set()
kill_it=[]
for tup in dummy_s:
if tup[0] not in allowed or tup[1] not in allowed:
allowed.add(tup[0]);allowed.add(tup[1])
else:
kill_it.append(tup)
for tupk in kill_it:
dummy_s.remove(tupk)
#dummy_top=dummy_s[0:(max(len(indivcol1),len(indivcol2))+1)]
length2=[(trip[0],trip[1]) for trip in dummy_s]
'''for trip in dummy_top:
length2.append((trip[0],trip[1]))'''
l2hL+=[length2]
newhits.add(length2)
holesList+=[dummy_top]
elif len(htsc)==2:
for i in range(1,2):
if getInt(htsc[i-1][0])< getInt(htsc[i][0]):
if getInt(htsc[i-1][1])< getInt(htsc[i][1]):
if getInt(htsc[i-1][0])<(getInt(htsc[i][0])-1) and getInt(htsc[i-1][1])<(getInt(htsc[i][1])-1):#if there is a hole on BOTH scafs
#there was a gap on the scaffold. now we want to fill it in.
indivcol1=set(range(getInt(htsc[i-1][0])+1),getInt(htsc[i][0]))
indivcol2=set(range(getInt(htsc[i-1][1])+1),getInt(htsc[i][1]))
mycol=indivcol1.union(indivcol2)
dummy=[]
with open(en_pslout_file,'r') as en_pslout:
for line in en_pslout:
line=line.rstrip().split()
if getInt(line[0]) in mycol and getInt(line[1]) in mycol and pbi[line[0]]!=pbi[line[1]]:
dummy.append((line[0],line[1],(float(line[-3]),float(line[-2]))))#we now have a tuple with the ohnologan, & its bitscore&ev
dummy_s=sorted(dummy,key=lambda tup:(tup[2][0]),reverse=True)
allowed=set()
kill_it=[]
for tup in dummy_s:
if tup[0] not in allowed or tup[1] not in allowed:
allowed.add(tup[0]);allowed.add(tup[1])
else:
kill_it.append(tup)
for tupk in kill_it:
dummy_s.remove(tupk)
#dummy_top=dummy_s[0:(max(len(indivcol1),len(indivcol2))+1)]
length2=[(trip[0],trip[1]) for trip in dummy_s]
'''for trip in dummy_top:
length2.append((trip[0],trip[1]))'''
l2thhL+=[length2]
newhits.add(length2)
twohitsholesList+=[dummy_top]
elif getInt(htsc[i-1][1])> getInt(htsc[i][1]) and getInt(htsc[i][1])> getInt(htsc[i+1][1]):#case: scafs in reverse order
if getInt(htsc[i-1][0])<(getInt(htsc[i][0])-1) and getInt(htsc[i-1][1])>(getInt(htsc[i][1])+1):#if there is a hole on BOTH scafs
indivcol1=set(range(getInt(htsc[i-1][0])+1),getInt(htsc[i][0]))
indivcol2=set(range(getInt(htsc[i-1][1])-1),getInt(htsc[i][1]),-1)
mycol=indivcol1.union(indivcol2)
dummy=[]
with open(en_pslout_file,'r') as en_pslout:
for line in en_pslout:
if getInt(line[0]) in mycol and getInt(line[1]) in mycol and pbi[line[0]]!=pbi[line[1]]:#line[1]!=line[3]:
dummy.append((line[0],line[1],(float(line[-3]),float(line[-2]))))#we now have a tuple with the ohnologan, & its bitscore&ev
dummy_s=sorted(dummy,key=lambda tup:(tup[2][0]),reverse=True)
allowed=set()
kill_it=[]
for tup in dummy_s:
if tup[0] not in allowed or tup[1] not in allowed:
allowed.add(tup[0]);allowed.add(tup[1])
else:
kill_it.append(tup)
for tupk in kill_it:
dummy_s.remove(tupk)
#dummy_top=dummy_s[0:(max(len(indivcol1),len(indivcol2))+1)]
length2=[(trip[0],trip[1]) for trip in dummy_s]
'''for trip in dummy_top:
length2.append((trip[0],trip[1]))'''
l2thhL+=[length2]
newhits.add(length2)
twohitsholesList+=[dummy_top] #i think this will make thhL a list of lists, one list for each sca-sca pair
#which may be good, or bad, but it is easy to change
#twohitsholesList+=sorted(dummy,key=lambda tup:(tup[2][0]),reverse=True)[0:(min(len(indivcol1),len(indivcol2))+1)]
for t in newhits:
htsc+=[t]
htsc=sorted(htsc,key=lambda tup: (tup[0]))
return holesList, l2hL, twohitsholesList, l2thhL, htscList
def printht(htsc):
md=[]
ml=[]
if len(htsc)>2:
for i in range(1,len(htsc)-1):
if getInt(htsc[i-1][0])< getInt(htsc[i][0]) and getInt(htsc[i][0])< getInt(htsc[i+1][0]):
if getInt(htsc[i-1][1])< getInt(htsc[i][1]) and getInt(htsc[i][1])< getInt(htsc[i+1][1]):
if i==1:
ml+=[htsc[i-1],htsc[i],htsc[i+1]]
elif i>1:
ml+=[htsc[i+1]]
elif getInt(htsc[i-1][1])> getInt(htsc[i][1]) and getInt(htsc[i][1])> getInt(htsc[i+1][1]):
if i==1:
ml+=[htsc[i-1],htsc[i],htsc[i+1]]
elif i>1:
ml+=[htsc[i+1]]
else:
print 'failed:', htsc[i]
print ml
elif len(htsc)==2:
if getInt(htsc[0][0])< getInt(htsc[1][0]):
if getInt(htsc[0][1])> getInt(htsc[1][1]):
md+=[htsc[0]]
md+=[htsc[1]]
elif getInt(htsc[0][1])<getInt(htsc[1][1]):
md+=[htsc[0]]
md+=[htsc[1]]
print md
else:
print 'single : ', htsc
def getdup2(lst):
d={}
dd={}
for key, value in lst:
d[value] = d.get(value, []) + [key]
for k in d.keys():
if len(d[k])==1:
print ','.join(d[k]), k
else:
print 'dup: ',','.join( d[k]),"-->", k
def getdupboth(lst):
d1={}
d2={}
for k,v in lst:
if k in d1:
d1[k]+=[v]
else:
d1[k]=[v]
if v in d2 :
d2[v]+=[k]
else:
d2[v]+=[k]
for k1 in d1:
print k1,':',d1[k1]
for k2 in d2:
#if len(d2[k2])==1:
print d2[k2],':',k2
def pdup(d):
for k in d:
if len(d[k])==1:
print (k,d[k])
else:
print 'dup:',(k,d[k])
def prTp(lst):
for k in lst:
print k[0],k[1]
def getCts(lst):
recip=[]
recipC=0
oneway=[]
onewayC=0
clst=copy.copy(lst)
recip_seen=[]
for (k,v) in clst:
if (v,k) in clst:
if (v,k) not in recip_seen:
recip_seen.append((k,v))
recip_seen.append((v,k))
recipC+=1
elif (v,k) not in clst:
oneway.append((k,v))
onewayC+=1
# print 'Reciprocal hits : ', len(recip_seen),recipC
# print 'One way Hits : ', len(oneway), onewayC
def getDistrib(lst,diPL):
d=[]
seen=[]
for k,v in lst:
if (v,k) not in seen:
t=float(diPL[k]) / float(diPL[v])
if t > 1.0:
t=1/t
d.append(t)
seen.append((k,v))
return d
#Read in and update the psl output and find hits
def readpsl(pslout,pbidict):
bhits=[]
hits=collections.OrderedDict()
phits=collections.OrderedDict()
scaffolds={}
Lengthprot={}
ps=collections.OrderedDict()
with open(pslout,'r') as file:
for line in file:
line=line.rstrip().split()
ov=max([ int(i) for i in re.split(r'(\d+)',line[-1]) if len(i)>0 and i.isdigit()])
if float(line[4])>40.0 and ov/min(float(line[5]),float(line[6]))>=0.12:
if line[0]!=line[2]:
if line[1] not in hits.keys():
hits[line[1]]=[line[3]]
else:
hits[line[1]].append(line[3])
if line[0] not in phits.keys():
phits[line[0]]={line[2]:line[-2]}
else:
phits[line[0]][line[2]]=line[-2]
if line[1] not in scaffolds.keys():
scaffolds[line[1]]=[line[0]]
else:
scaffolds[line[1]].append(line[0])
if line[3] not in scaffolds.keys():
scaffolds[line[3]]=[line[2]]
else:
scaffolds[line[3]].append(line[2])
if line[1] in ps:
if line[3] in ps[line[1]].keys():
ps[line[1]][line[3]]+=[(line[0],line[2],line[-2])]
else:
ps[line[1]][line[3]]=[(line[0],line[2],line[-2])]
else:
ps[line[1]]={}
ps[line[1]][line[3]]=[(line[0],line[2],line[-2])]
if line[0] not in Lengthprot:
Lengthprot[line[0]]=int(line[5])
if line[2] not in Lengthprot:
Lengthprot[line[2]]=int(line[6])
for key in hits:
kval=collections.Counter(hits[key])
hits[key]=dict([a,-math.log(float(x)/sum(kval.values()))] for a, x in kval.iteritems())
for k1 in hits:
for k2 in hits[k1]:
score1=0
score2=0
try:
score1=hits[k1][k2]
except:
score1=10
try:
score2=hits[k2][k1]
except:
score2=10
score=score1+score2
bhits.append((k1,k2,score))
ghits=collections.OrderedDict()
for p1 in phits.keys():
minval=min([float(phits[p1][p2]) for p2 in phits[p1].keys()])
uplimit=float(minval*10**10)
check=0
for p2 in phits[p1]:
if float(phits[p1][p2]) <=uplimit:
if p1 not in ghits.keys():
ghits[p1]={}
ghits[p1][p2]=float(phits[p1][p2])
else:
ghits[p1][p2]=float(phits[p1][p2])
if float(phits[p1][p2])==minval and check==0:
print p1,p2
check=1
betterHits=collections.OrderedDict()
pairs=[]
return
for g in ghits.keys():
score=15.0
bh=None
if pbidict[g] not in betterHits.keys():
betterHits[pbidict[g]]={}
# print 'P1: ', g
for g2 in ghits[g].keys():
# print 'P2',g2, ghits[g][g2],hits[pbidict[g]][pbidict[g2]]
if hits[pbidict[g]][pbidict[g2]]<score:
bh=g2
score=hits[pbidict[g]][pbidict[g2]]
pairs.append((g,bh))
if pbidict[bh] not in betterHits[pbidict[g]].keys():
betterHits[pbidict[g]][pbidict[bh]]=[(g,bh)]
else:
betterHits[pbidict[g]][pbidict[bh]].append((g,bh))
getCts(pairs)
# print getDistrib(pairs,Lengthprot)
for k in betterHits.keys():
for g in betterHits[k].keys():
htsc=sorted(betterHits[k][g],key=lambda tup: (tup[0]))
gh=[]
## get scaffolds dictionary
def readScaf(psl):
scaffolds={}
filename=open(psl,"r")
for line in filename:
line=line.rstrip().split()
if line[1] in scaffolds and line[3] in scaffolds[line[1]]:
scaffolds[line[1]][line[3]]+=[(line[0],line[2],line[-2])]
else:
scaffolds[line[1]]={line[3]:[(line[0],line[2],line[-2])]}
## create htsc from best hits ouput
def createHTSC(bihits,pbidict):
sca_sca_hits=collections.OrderedDict()
with open(bihits,'r')as file:
for line in file:
line=line.rstrip().split()
if pbidict[line[0]] not in sca_sca_hits.keys():
sca_sca_hits[pbidict[line[0]]]=collections.OrderedDict()
if pbidict[line[1]] not in sca_sca_hits[pbidict[line[0]]].keys():
sca_sca_hits[pbidict[line[0]]][pbidict[line[1]]]=[(line[0],line[1])]
else:
sca_sca_hits[pbidict[line[0]]][pbidict[line[1]]].append((line[0],line[1]))
else:
if pbidict[line[1]] not in sca_sca_hits[pbidict[line[0]]].keys():
sca_sca_hits[pbidict[line[0]]][pbidict[line[1]]]=[(line[0],line[1])]
else:
sca_sca_hits[pbidict[line[0]]][pbidict[line[1]]].append((line[0],line[1]))
return sca_sca_hits
#Read he gff3 files and create a dictionary: scaffolds: list of proteins
def readgff(f):
filename = open(f, "r")
scaffolds=collections.OrderedDict()
pbi=collections.OrderedDict()
for line in filename:
line=line.strip().split()
if line[0][:8]=='scaffold' and line[2]=='mRNA':
#pt=re.split(r'[=;\s]',line[8])[1]
pbi[re.split(r'[=;\s]',line[8])[1]]=line[0]
if line[0] not in scaffolds.keys():
scaffolds[line[0]]=[re.split(r'[=;\s]',line[8])[1]]
else:
scaffolds[line[0]].append(re.split(r'[=;\s]',line[8])[1])
for k in scaffolds.keys():
scaffolds[k]=sorted(scaffolds[k])
return pbi,scaffolds
if __name__ == '__main__':
ProcessCLI(sys.argv)