Mercurial > repos > miller-lab > genome_diversity
annotate cluster_onConnctdComps.py @ 39:e56023008e36 default tip
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author | miller-lab |
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date | Mon, 06 Jul 2015 10:32:24 -0400 |
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1 #!/usr/bin/env python |
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2 # -*- coding: utf-8 -*- |
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3 # |
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4 # Cluster_GOKEGG.py |
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5 # |
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6 # Copyright 2013 Oscar Reina <oscar@niska.bx.psu.edu> |
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7 # |
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8 # This program is free software; you can redistribute it and/or modify |
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9 # it under the terms of the GNU General Public License as published by |
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10 # the Free Software Foundation; either version 2 of the License, or |
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11 # (at your option) any later version. |
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12 # |
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13 # This program is distributed in the hope that it will be useful, |
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14 # but WITHOUT ANY WARRANTY; without even the implied warranty of |
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15 # MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the |
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16 # GNU General Public License for more details. |
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17 # |
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18 # You should have received a copy of the GNU General Public License |
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19 # along with this program; if not, write to the Free Software |
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20 # Foundation, Inc., 51 Franklin Street, Fifth Floor, Boston, |
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21 # MA 02110-1301, USA. |
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22 |
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23 import argparse |
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24 import os |
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25 from networkx import connected_components,Graph,clustering |
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26 from numpy import percentile |
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27 from decimal import Decimal,getcontext |
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28 from itertools import permutations,combinations |
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29 import sys |
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30 |
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31 def rtrnClustrsOnCltrCoff(dNodesWeightMin,threshold,perctile=True): |
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32 """ |
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33 From a file with three columns: nodeA, nodeB and a score, it returns |
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34 the strong and weak connected components produced when the edges |
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35 below the percentage threshold (or value) are excluded. |
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36 """ |
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37 #~ |
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38 Gmin = Graph() |
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39 for nodeA,nodeB in dNodesWeightMin: |
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40 wMin=dNodesWeightMin[nodeA,nodeB] |
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41 Gmin.add_edge(nodeA,nodeB,weight=wMin) |
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42 #~ |
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43 clstrCoffcMin=clustering(Gmin,weight='weight') |
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44 #~ |
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45 if perctile: |
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46 umbralMin=percentile(clstrCoffcMin.values(),threshold) |
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47 else: |
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48 umbralMin=threshold |
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49 #~ |
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50 GminNdsRmv=[x for x in clstrCoffcMin if clstrCoffcMin[x]<umbralMin] |
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51 #~ |
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52 Gmin.remove_nodes_from(GminNdsRmv) |
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53 #~ |
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54 dTermCmptNumbWkMin=rtrndata(Gmin) |
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55 #~ |
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56 salelClustr=[] |
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57 srtdterms=sorted(dTermCmptNumbWkMin.keys()) |
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58 for echTerm in srtdterms: |
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59 try: |
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60 MinT=dTermCmptNumbWkMin[echTerm] |
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61 except: |
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62 MinT='-' |
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63 salelClustr.append('\t'.join([echTerm,MinT])) |
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64 #~ |
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65 return salelClustr |
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66 |
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67 def rtrndata(G): |
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68 """ |
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69 returna list of terms and its clustering, as well as clusters from |
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70 a networkx formatted file. |
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71 """ |
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72 #~ |
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73 cntCompnts=0 |
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74 dTermCmptNumbWk={} |
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75 for echCompnt in connected_components(G): |
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76 cntCompnts+=1 |
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77 #print '.'.join(echCompnt) |
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78 for echTerm in echCompnt: |
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79 dTermCmptNumbWk[echTerm]=str(cntCompnts) |
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80 #~ |
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81 return dTermCmptNumbWk |
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82 |
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83 def rtrnCATcENSEMBLc(inCATfile,classClmns,ENSEMBLTcolmn,nonHdr=True): |
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84 """ |
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85 return a dictionary of all the categories in an input file with |
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86 a set of genes. Takes as input a file with categories an genes. |
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87 """ |
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88 dCAT={} |
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89 dENSEMBLTCAT={} |
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90 for eachl in open(inCATfile,'r'): |
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91 if nonHdr and eachl.strip(): |
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92 ENSEMBLT=eachl.splitlines()[0].split('\t')[ENSEMBLTcolmn] |
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93 sCAT=set() |
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94 for CATcolmn in classClmns: |
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95 sCAT.update(set([x for x in eachl.splitlines()[0].split('\t')[CATcolmn].split('.')])) |
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96 sCAT=sCAT.difference(set(['','U','N'])) |
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97 if len(sCAT)>0: |
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98 dENSEMBLTCAT[ENSEMBLT]=sCAT |
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99 for CAT in sCAT: |
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100 try: |
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101 dCAT[CAT].add(ENSEMBLT) |
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102 except: |
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103 dCAT[CAT]=set([ENSEMBLT]) |
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104 nonHdr=True |
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105 #~ |
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106 dCAT=dict([(x,len(dCAT[x])) for x in dCAT.keys()]) |
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107 #~ |
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108 return dCAT,dENSEMBLTCAT |
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109 |
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110 |
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111 def calcDistance(sCAT1,sCAT2): |
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112 """ |
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113 takes as input two set of genesin different categories and returns |
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114 a value 1-percentage of gene shared cat1->cat2, and cat2->cat1. |
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115 """ |
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116 getcontext().prec=5 |
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117 lgensS1=Decimal(len(sCAT1)) |
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118 lgensS2=Decimal(len(sCAT2)) |
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119 shrdGns=sCAT1.intersection(sCAT2) |
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120 lenshrdGns=len(shrdGns) |
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121 #~ |
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122 dC1C2=1-(lenshrdGns/lgensS1) |
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123 dC2C1=1-(lenshrdGns/lgensS2) |
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124 #~ |
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125 return dC1C2,dC2C1 |
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126 |
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127 def rtnPrwsdtncs(dCAT,dENSEMBLTCAT): |
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128 """ |
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129 return a mcl formated pairwise distances from a list of categories |
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130 """ |
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131 #~ |
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132 getcontext().prec=5 |
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133 dCATdst={} |
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134 lENSEMBL=dENSEMBLTCAT.keys() |
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135 l=len(lENSEMBL) |
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136 c=0 |
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137 for ENSEMBL in lENSEMBL: |
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138 c+=1 |
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139 lCAT=dENSEMBLTCAT.pop(ENSEMBL) |
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140 for CAT1,CAT2 in combinations(lCAT, 2): |
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141 try: |
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142 dCATdst[CAT1,CAT2]+=1 |
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143 except: |
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144 dCATdst[CAT1,CAT2]=1 |
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145 try: |
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146 dCATdst[CAT2,CAT1]+=1 |
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147 except: |
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148 dCATdst[CAT2,CAT1]=1 |
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149 #~ |
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150 dNodesWeightMin={} |
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151 l=len(dCATdst) |
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152 for CAT1,CAT2 in dCATdst.keys(): |
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153 shrdGns=dCATdst.pop((CAT1,CAT2)) |
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154 dC1C2=float(shrdGns) |
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155 nodeA,nodeB=sorted([CAT1,CAT2]) |
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156 try: |
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157 cscor=dNodesWeightMin[nodeA,nodeB] |
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158 if cscor>=dC1C2: |
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159 dNodesWeightMin[nodeA,nodeB]=dC1C2 |
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160 except: |
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161 dNodesWeightMin[nodeA,nodeB]=dC1C2 |
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162 # |
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163 return dNodesWeightMin |
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164 |
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165 def parse_class_columns(val, max_col): |
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166 int_list = [] |
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167 |
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168 for elem in [x.strip() for x in val.split(',')]: |
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169 if elem[0].lower() != 'c': |
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170 print >> sys.stderr, "bad column format:", elem |
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171 sys.exit(1) |
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172 |
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173 int_val = as_int(elem[1:]) |
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174 |
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175 if int_val is None: |
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176 print >> sys.stderr, "bad column format:", elem |
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177 sys.exit(1) |
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178 elif not 1 <= int_val <= max_col: |
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179 print >> sys.stderr, "column out of range:", elem |
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180 sys.exit(1) |
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181 |
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182 int_list.append(int_val - 1) |
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183 |
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184 return int_list |
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185 |
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186 def as_int(val): |
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187 try: |
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188 return int(val) |
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189 except ValueError: |
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190 return None |
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191 else: |
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192 raise |
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193 |
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194 def main(): |
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195 """ |
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196 """ |
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197 #~ bpython cluster_onConnctdComps.py --input=../conctFinal_CEU.tsv --outfile=../borrar.txt --threshold=90 --ENSEMBLTcolmn=1 --classClmns='20 22' |
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198 parser = argparse.ArgumentParser(description='Returns the count of genes in ...') |
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199 parser.add_argument('--input',metavar='input TXT file',type=str,help='the input file with the table in txt format.',required=True) |
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200 parser.add_argument('--input_columns',metavar='input INT value',type=int,help='the number of columns in the input file.',required=True) |
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201 parser.add_argument('--outfile',metavar='input TXT file',type=str,help='the output file with the connected components.',required=True) |
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202 parser.add_argument('--threshold',metavar='input FLOAT value',type=float,help='the threshold to disconnect the nodes.',required=True) |
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203 parser.add_argument('--ENSEMBLTcolmn',metavar='input INT file',type=int,help='the column with the ENSEMBLE code in the input.',required=True) |
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204 parser.add_argument('--classClmns',metavar='input STR value',type=str,help='the list of columns with the gene categories separated by space.',required=True) |
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205 args = parser.parse_args() |
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206 infile = args.input |
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207 threshold = args.threshold |
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208 outfile = args.outfile |
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209 ENSEMBLTcolmn = args.ENSEMBLTcolmn |
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210 classClmns = parse_class_columns(args.classClmns, args.input_columns) |
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211 #~ |
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212 dCAT,dENSEMBLTCAT=rtrnCATcENSEMBLc(infile,classClmns,ENSEMBLTcolmn) |
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213 dNodesWeightMin=rtnPrwsdtncs(dCAT,dENSEMBLTCAT) |
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214 salelClustr=rtrnClustrsOnCltrCoff(dNodesWeightMin,threshold) |
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215 #~ |
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216 with open(outfile, 'w') as salef: |
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217 print >> salef, '\n'.join(salelClustr) |
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218 #~ |
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219 #~ |
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220 |
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221 if __name__ == '__main__': |
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222 main() |
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223 |