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1 # Copyright INRA (Institut National de la Recherche Agronomique)
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2 # http://www.inra.fr
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3 # http://urgi.versailles.inra.fr
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4 #
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5 # This software is governed by the CeCILL license under French law and
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6 # abiding by the rules of distribution of free software. You can use,
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7 # modify and/ or redistribute the software under the terms of the CeCILL
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8 # license as circulated by CEA, CNRS and INRIA at the following URL
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9 # "http://www.cecill.info".
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10 #
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11 # As a counterpart to the access to the source code and rights to copy,
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12 # modify and redistribute granted by the license, users are provided only
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13 # with a limited warranty and the software's author, the holder of the
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14 # economic rights, and the successive licensors have only limited
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15 # liability.
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16 #
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17 # In this respect, the user's attention is drawn to the risks associated
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18 # with loading, using, modifying and/or developing or reproducing the
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19 # software by the user in light of its specific status of free software,
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20 # that may mean that it is complicated to manipulate, and that also
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21 # therefore means that it is reserved for developers and experienced
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22 # professionals having in-depth computer knowledge. Users are therefore
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23 # encouraged to load and test the software's suitability as regards their
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24 # requirements in conditions enabling the security of their systems and/or
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25 # data to be ensured and, more generally, to use and operate it in the
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26 # same conditions as regards security.
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27 #
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28 # The fact that you are presently reading this means that you have had
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29 # knowledge of the CeCILL license and that you accept its terms.
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30
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31
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32 import sys
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33 from commons.core.seq.BioseqDB import BioseqDB
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34 from commons.core.seq.Bioseq import Bioseq
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35 from commons.core.coord.Align import Align
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36 from commons.core.coord.Range import Range
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37 from commons.core.stat.Stat import Stat
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38 from math import log
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39
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40
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41 ## Multiple Sequence Alignment Representation
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42 #
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43 #
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44 class AlignedBioseqDB( BioseqDB ):
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45
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46 def __init__( self, name="" ):
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47 BioseqDB.__init__( self, name )
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48 seqLength = self.getLength()
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49 if self.getSize() > 1:
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50 for bs in self.db[1:]:
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51 if bs.getLength() != seqLength:
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52 print "ERROR: aligned sequences have different length"
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53
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54
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55 ## Get length of the alignment
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56 #
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57 # @return length
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58 # @warning name before migration was 'length'
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59 #
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60 def getLength( self ):
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61 length = 0
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62 if self.db != []:
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63 length = self.db[0].getLength()
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64 return length
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65
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66
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67 ## Get the true length of a given sequence (without gaps)
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68 #
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69 # @param header string header of the sequence to analyze
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70 # @return length integer
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71 # @warning name before migration was 'true_length'
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72 #
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73 def getSeqLengthWithoutGaps( self, header ):
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74 bs = self.fetch( header )
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75 count = 0
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76 for pos in xrange(0,len(bs.sequence)):
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77 if bs.sequence[pos] != "-":
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78 count += 1
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79 return count
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80
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18
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81 def cleanMSA( self ):
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82 #TODO: Refactoring
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83 """clean the MSA"""
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84 i2del = []
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85
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86 # for each sequence in the MSA
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87 for seqi in xrange(0,self.getSize()):
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88 if seqi in i2del:
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89 continue
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90 #define it as the reference
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91 ref = self.db[seqi].sequence
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92 refHeader = self.db[seqi].header
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93 # for each following sequence
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94 for seq_next in xrange(seqi+1,self.getSize()):
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95 if seq_next in i2del:
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96 continue
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97 keep = 0
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98 # for each position along the MSA
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99 for posx in xrange(0,self.getLength()):
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100 seq = self.db[seq_next].sequence
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101 if seq[posx] != '-' and ref[posx] != '-':
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102 keep = 1
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103 break
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104 seqHeader = self.db[seq_next].header
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105 # if there is at least one gap between the ref seq and the other seq
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106 # keep track of the shortest by recording it in "i2del"
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107 if keep == 0:
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108
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109 if self.getSeqLengthWithoutGaps(refHeader) < self.getSeqLengthWithoutGaps(seqHeader):
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110 if seqi not in i2del:
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111 i2del.append( seqi )
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112 else:
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113 if seq_next not in i2del:
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114 i2del.append( seq_next )
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115
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116 # delete from the MSA each seq present in the list "i2del"
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117 for i in reversed(sorted(set(i2del))):
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118 del self.db[i]
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119
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120 self.idx = {}
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121 count = 0
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122 for i in self.db:
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123 self.idx[i.header] = count
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124 count += 1
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125
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6
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126 ## Record the occurrences of symbols (A, T, G, C, N, -, ...) at each site
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127 #
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128 # @return: list of dico whose keys are symbols and values are their occurrences
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129 #
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130 def getListOccPerSite( self ):
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131 lOccPerSite = [] # list of dictionaries, one per position on the sequence
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132 n = 0 # nb of sequences parsed from the input file
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133 firstSeq = True
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134
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135 # for each sequence in the bank
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136 for bs in self.db:
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137 if bs.sequence == None:
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138 break
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139 n += 1
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140
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141 # if it is the first to be parsed, create a dico at each site
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142 if firstSeq:
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143 for i in xrange(0,len(bs.sequence)):
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144 lOccPerSite.append( {} )
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145 firstSeq = False
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146
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147 # for each site, add its nucleotide
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148 for i in xrange(0,len(bs.sequence)):
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149 nuc = bs.sequence[i].upper()
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150 if lOccPerSite[i].has_key( nuc ):
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151 lOccPerSite[i][nuc] += 1
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152 else:
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153 lOccPerSite[i][nuc] = 1
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154
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155 return lOccPerSite
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156
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157 #TODO: review minNbNt !!! It should be at least 2 nucleotides to build a consensus...
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158 ## Make a consensus from the MSA
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159 #
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160 # @param minNbNt: minimum nb of nucleotides to edit a consensus
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161 # @param minPropNt: minimum proportion for the major nucleotide to be used, otherwise add 'N' (default=0.0)
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162 # @param verbose: level of information sent to stdout (default=0/1)
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163 # @return: consensus
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164 #
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165 def getConsensus( self, minNbNt, minPropNt=0.0, verbose=0 , isHeaderSAtannot=False):
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166
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167 maxPropN = 0.40 # discard consensus if more than 40% of N's
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168
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169 nbInSeq = self.getSize()
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170 if verbose > 0:
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171 print "nb of aligned sequences: %i" % ( nbInSeq ); sys.stdout.flush()
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172 if nbInSeq < 2:
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173 print "ERROR: can't make a consensus with less than 2 sequences"
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174 sys.exit(1)
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175 if minNbNt >= nbInSeq:
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176 minNbNt = nbInSeq - 1
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177 print "minNbNt=%i" % ( minNbNt )
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178 if minPropNt >= 1.0:
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179 print "ERROR: minPropNt=%.2f should be a proportion (below 1.0)" % ( minPropNt )
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180 sys.exit(1)
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181
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182 lOccPerSite = self.getListOccPerSite()
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183 nbSites = len(lOccPerSite)
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184 if verbose > 0:
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185 print "nb of sites: %i" % ( nbSites ); sys.stdout.flush()
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186
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187 seqConsensus = ""
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188
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189 # for each site (i.e. each column of the MSA)
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190 nbRmvColumns = 0
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191 countSites = 0
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192 for dNt2Occ in lOccPerSite:
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193 countSites += 1
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194 if verbose > 1:
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195 print "site %s / %i" % ( str(countSites).zfill( len(str(nbSites)) ),
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196 nbSites )
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197 sys.stdout.flush()
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198 occMaxNt = 0 # occurrences of the predominant nucleotide at this site
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199 lBestNt = []
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200 nbNt = 0 # total nb of A, T, G and C (no gap)
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201
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202 # for each distinct symbol at this site (A, T, G, C, N, -,...)
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203 for j in dNt2Occ.keys():
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204 if j != "-":
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205 nbNt += dNt2Occ[j]
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206 if verbose > 1:
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207 print "%s: %i" % ( j, dNt2Occ[j] )
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208 if dNt2Occ[j] > occMaxNt:
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209 occMaxNt = dNt2Occ[j]
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210 lBestNt = [ j ]
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211 elif dNt2Occ[j] == occMaxNt:
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212 lBestNt.append( j )
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213 if nbNt == 0: # some MSA programs can remove some sequences (e.g. Muscle after Recon) or when using Refalign (non-alignable TE fragments put together via a refseq)
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214 nbRmvColumns += 1
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215
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216 if len( lBestNt ) >= 1:
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217 bestNt = lBestNt[0]
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218
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219 # if the predominant nucleotide occurs in less than x% of the sequences, put a "N"
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220 if minPropNt > 0.0 and nbNt != 0 and float(occMaxNt)/float(nbNt) < minPropNt:
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221 bestNt = "N"
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222
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223 if int(nbNt) >= int(minNbNt):
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224 seqConsensus += bestNt
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225 if verbose > 1:
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226 print "-> %s" % ( bestNt )
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227
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228 if nbRmvColumns:
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229 if nbRmvColumns == 1:
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230 print "WARNING: 1 site was removed (%.2f%%)" % (nbRmvColumns / float(nbSites) * 100)
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231 else:
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232 print "WARNING: %i sites were removed (%.2f%%)" % ( nbRmvColumns, nbRmvColumns / float(nbSites) * 100 )
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233 sys.stdout.flush()
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234 if seqConsensus == "":
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235 print "WARNING: no consensus can be built (no sequence left)"
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236 return
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237
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238 propN = seqConsensus.count("N") / float(len(seqConsensus))
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239 if propN >= maxPropN:
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240 print "WARNING: no consensus can be built (%i%% of N's >= %i%%)" % ( propN * 100, maxPropN * 100 )
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241 return
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242 elif propN >= maxPropN * 0.5:
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243 print "WARNING: %i%% of N's" % ( propN * 100 )
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244
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245 consensus = Bioseq()
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246 consensus.sequence = seqConsensus
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247 if isHeaderSAtannot:
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248 header = self.db[0].header
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249 pyramid = header.split("Gr")[1].split("Cl")[0]
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250 pile = header.split("Cl")[1].split(" ")[0]
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251 consensus.header = "consensus=%s length=%i nbAlign=%i pile=%s pyramid=%s" % (self.name, len(seqConsensus), self.getSize(), pile, pyramid)
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252 else:
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253 consensus.header = "consensus=%s length=%i nbAlign=%i" % ( self.name, len(seqConsensus), self.getSize() )
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254
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255 if verbose > 0:
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256
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257 statEntropy = self.getEntropy( verbose - 1 )
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258 print "entropy: %s" % ( statEntropy.stringQuantiles() )
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259 sys.stdout.flush()
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260
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261 return consensus
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262
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263
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264 ## Get the entropy of the whole multiple alignment (only for A, T, G and C)
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265 #
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266 # @param verbose level of verbosity
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267 #
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268 # @return statistics about the entropy of the MSA
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269 #
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270 def getEntropy( self, verbose=0 ):
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271
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272 stats = Stat()
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273
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274 # get the occurrences of symbols at each site
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275 lOccPerSite = self.getListOccPerSite()
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276
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277 countSite = 0
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278
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279 # for each site
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280 for dSymbol2Occ in lOccPerSite:
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281 countSite += 1
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282
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283 # count the number of nucleotides (A, T, G and C, doesn't count gap '-')
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284 nbNt = 0
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285 dATGC2Occ = {}
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286 for base in ["A","T","G","C"]:
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287 dATGC2Occ[ base ] = 0.0
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288 for nt in dSymbol2Occ.keys():
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289 if nt != "-":
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290 nbNt += dSymbol2Occ[ nt ]
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291 checkedNt = self.getATGCNFromIUPAC( nt )
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292 if checkedNt in ["A","T","G","C"] and dSymbol2Occ.has_key( checkedNt ):
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293 dATGC2Occ[ checkedNt ] += 1 * dSymbol2Occ[ checkedNt ]
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294 else: # for 'N'
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295 if dSymbol2Occ.has_key( checkedNt ):
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296 dATGC2Occ[ "A" ] += 0.25 * dSymbol2Occ[ checkedNt ]
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297 dATGC2Occ[ "T" ] += 0.25 * dSymbol2Occ[ checkedNt ]
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298 dATGC2Occ[ "G" ] += 0.25 * dSymbol2Occ[ checkedNt ]
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299 dATGC2Occ[ "C" ] += 0.25 * dSymbol2Occ[ checkedNt ]
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300 if verbose > 2:
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301 for base in dATGC2Occ.keys():
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302 print "%s: %i" % ( base, dATGC2Occ[ base ] )
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303
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304 # compute the entropy for the site
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305 entropySite = 0.0
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306 for nt in dATGC2Occ.keys():
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307 entropySite += self.computeEntropy( dATGC2Occ[ nt ], nbNt )
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308 if verbose > 1:
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309 print "site %i (%i nt): entropy = %.3f" % ( countSite, nbNt, entropySite )
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310 stats.add( entropySite )
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311
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312 return stats
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313
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314
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315 ## Get A, T, G, C or N from an IUPAC letter
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316 # IUPAC = ['A','T','G','C','U','R','Y','M','K','W','S','B','D','H','V','N']
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317 #
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318 # @return A, T, G, C or N
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319 #
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320 def getATGCNFromIUPAC( self, nt ):
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321 iBs = Bioseq()
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322 return iBs.getATGCNFromIUPAC( nt )
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323
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324
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325 ## Compute the entropy based on the occurrences of a certain nucleotide and the total number of nucleotides
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326 #
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327 def computeEntropy( self, nbOcc, nbNt ):
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328 if nbOcc == 0.0:
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329 return 0.0
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330 else:
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331 freq = nbOcc / float(nbNt)
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332 return - freq * log(freq) / log(2)
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333
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334
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335 ## Save the multiple alignment as a matrix with '0' if gap, '1' otherwise
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336 #
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337 def saveAsBinaryMatrix( self, outFile ):
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338 outFileHandler = open( outFile, "w" )
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339 for bs in self.db:
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340 string = "%s" % ( bs.header )
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341 for nt in bs.sequence:
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342 if nt != "-":
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343 string += "\t%i" % ( 1 )
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344 else:
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345 string += "\t%i" % ( 0 )
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346 outFileHandler.write( "%s\n" % ( string ) )
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347 outFileHandler.close()
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348
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349
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350 ## Return a list of Align instances corresponding to the aligned regions (without gaps)
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351 #
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352 # @param query string header of the sequence considered as query
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353 # @param subject string header of the sequence considered as subject
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354 #
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355 def getAlignList( self, query, subject ):
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356 lAligns = []
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357 alignQ = self.fetch( query ).sequence
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358 alignS = self.fetch( subject ).sequence
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359 createNewAlign = True
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360 indexAlign = 0
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361 indexQ = 0
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362 indexS = 0
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363 while indexAlign < len(alignQ):
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364 if alignQ[ indexAlign ] != "-" and alignS[ indexAlign ] != "-":
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365 indexQ += 1
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366 indexS += 1
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367 if createNewAlign:
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368 iAlign = Align( Range( query, indexQ, indexQ ),
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369 Range( subject, indexS, indexS ),
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370 0,
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371 int( alignQ[ indexAlign ] == alignS[ indexAlign ] ),
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372 int( alignQ[ indexAlign ] == alignS[ indexAlign ] ) )
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373 lAligns.append( iAlign )
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374 createNewAlign = False
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375 else:
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376 lAligns[-1].range_query.end += 1
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377 lAligns[-1].range_subject.end += 1
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378 lAligns[-1].score += int( alignQ[ indexAlign ] == alignS[ indexAlign ] )
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379 lAligns[-1].identity += int( alignQ[ indexAlign ] == alignS[ indexAlign ] )
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380 else:
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381 if not createNewAlign:
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382 lAligns[-1].identity = 100 * lAligns[-1].identity / lAligns[-1].getLengthOnQuery()
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383 createNewAlign = True
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384 if alignQ[ indexAlign ] != "-":
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385 indexQ += 1
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386 elif alignS[ indexAlign ] != "-":
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387 indexS += 1
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388 indexAlign += 1
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389 if not createNewAlign:
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390 lAligns[-1].identity = 100 * lAligns[-1].identity / lAligns[-1].getLengthOnQuery()
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391 return lAligns
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392
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393
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394 def removeGaps(self):
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395 for iBs in self.db:
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396 iBs.removeSymbol( "-" )
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397
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398 ## Compute mean per cent identity for MSA.
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399 # First sequence in MSA is considered as reference sequence.
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400 #
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401 #
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402 def computeMeanPcentIdentity(self):
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403 seqRef = self.db[0]
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404 sumPcentIdentity = 0
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405
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406 for seq in self.db[1:]:
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407 pcentIdentity = self._computePcentIdentityBetweenSeqRefAndCurrentSeq(seqRef, seq)
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408 sumPcentIdentity = sumPcentIdentity + pcentIdentity
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409
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410 nbSeq = len(self.db[1:])
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411 meanPcentIdentity = round (sumPcentIdentity/nbSeq)
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412
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413 return meanPcentIdentity
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414
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415 def _computePcentIdentityBetweenSeqRefAndCurrentSeq(self, seqRef, seq):
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416 indexOnSeqRef = 0
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417 sumIdentity = 0
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418 for nuclSeq in seq.sequence:
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419 nuclRef = seqRef.sequence[indexOnSeqRef]
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420
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421 if nuclRef != "-" and nuclRef == nuclSeq:
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422 sumIdentity = sumIdentity + 1
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423 indexOnSeqRef = indexOnSeqRef + 1
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424
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425 return float(sumIdentity) / float(seqRef.getLength()) * 100
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426
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427
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428
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429
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430
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431
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432
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433
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434
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435
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436
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437
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438
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439
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440
|
