annotate smart_toolShed/SMART/Java/Python/getDifference.py @ 0:e0f8dcca02ed

Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
author yufei-luo
date Thu, 17 Jan 2013 10:52:14 -0500
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e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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1 #! /usr/bin/env python
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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2 #
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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3 # Copyright INRA-URGI 2009-2010
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4 #
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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5 # This software is governed by the CeCILL license under French law and
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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6 # abiding by the rules of distribution of free software. You can use,
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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7 # modify and/ or redistribute the software under the terms of the CeCILL
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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8 # license as circulated by CEA, CNRS and INRIA at the following URL
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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9 # "http://www.cecill.info".
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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10 #
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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11 # As a counterpart to the access to the source code and rights to copy,
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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12 # modify and redistribute granted by the license, users are provided only
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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13 # with a limited warranty and the software's author, the holder of the
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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14 # economic rights, and the successive licensors have only limited
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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15 # liability.
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16 #
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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17 # In this respect, the user's attention is drawn to the risks associated
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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18 # with loading, using, modifying and/or developing or reproducing the
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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19 # software by the user in light of its specific status of free software,
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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20 # that may mean that it is complicated to manipulate, and that also
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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21 # therefore means that it is reserved for developers and experienced
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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22 # professionals having in-depth computer knowledge. Users are therefore
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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23 # encouraged to load and test the software's suitability as regards their
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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24 # requirements in conditions enabling the security of their systems and/or
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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25 # data to be ensured and, more generally, to use and operate it in the
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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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
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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29 # knowledge of the CeCILL license and that you accept its terms.
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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30 #
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31 """Restrict a transcript list with some parameters (regions)"""
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32
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33 from optparse import OptionParser
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34 from SMART.Java.Python.structure.Transcript import Transcript
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35 from SMART.Java.Python.structure.TranscriptContainer import TranscriptContainer
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36 from SMART.Java.Python.structure.TranscriptListsComparator import TranscriptListsComparator
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37 from commons.core.writer.Gff3Writer import Gff3Writer
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38 from commons.core.parsing.FastaParser import FastaParser
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39 from SMART.Java.Python.misc.Progress import Progress
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40
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41 class DifferenceGetter(object):
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42
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43 def __init__(self, verbosity):
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44 self.verbosity = verbosity
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45 self.annotationParser = None
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46 self.referenceParser = None
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47 self.sequenceParser = None
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48 self.transcriptCount = 1
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49 self.split = False
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50
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51 def createTranscript(self, chromosome, start, end):
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52 transcript = Transcript()
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53 transcript.setChromosome(chromosome)
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54 transcript.setDirection("+")
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55 transcript.setStart(start)
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56 transcript.setEnd(end)
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57 transcript.setName("region_%d" % self.transcriptCount)
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58 transcript.setTagValue("ID", "region_%d" % self.transcriptCount)
e0f8dcca02ed Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
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59 self.transcriptCount += 1
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60 return transcript
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61
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62 def setSplit(self, split):
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63 self.split = split
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64
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65 def setAnnotationFile(self, fileName, format):
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66 if fileName != None:
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67 self.annotationParser = TranscriptContainer(fileName, format, self.verbosity)
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68
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69 def setReferenceFile(self, fileName, format):
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70 if fileName != None:
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71 self.referenceParser = TranscriptContainer(fileName, format, self.verbosity)
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72
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73 def setSequenceFile(self, fileName):
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74 if fileName != None:
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75 self.sequenceParser = FastaParser(fileName, self.verbosity)
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76
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77 def setOutputFile(self, fileName):
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78 self.writer = Gff3Writer(fileName, self.verbosity)
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79
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80 def initialize(self):
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81 self.presence = {}
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82 for chromosome in self.sequenceParser.getRegions():
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83 self.presence[chromosome] = [[1, self.sequenceParser.getSizeOfRegion(chromosome)]]
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84
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85 def readTranscripts(self):
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86 nbTranscripts = self.annotationParser.getNbTranscripts()
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87 progress = Progress(nbTranscripts, "Parsing annotation file" , self.verbosity)
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88 for transcript in self.annotationParser.getIterator():
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89 chromosome = transcript.getChromosome()
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90 toBeDeleted = []
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91 toBeAppended = []
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92 for i, element in enumerate(self.presence[chromosome]):
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93 start, end = element
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94 if start <= transcript.getEnd() and transcript.getStart() <= end:
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95 toBeDeleted.append(i)
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96 if start < transcript.getStart():
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97 toBeAppended.append([start, transcript.getStart() - 1])
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98 if end > transcript.getEnd():
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99 toBeAppended.append([transcript.getEnd() + 1, end])
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100 for i in reversed(toBeDeleted):
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101 del self.presence[chromosome][i]
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102 self.presence[chromosome].extend(toBeAppended)
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103 progress.inc()
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104 progress.done()
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105
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106 def writeOutput(self):
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107 for chromosome in self.presence:
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108 for element in self.presence[chromosome]:
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109 start, end = element
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110 self.writer.addTranscript(self.createTranscript(chromosome, start, end))
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111 self.writer.write()
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112
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113 def compareToSequence(self):
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114 self.initialize()
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115 self.readTranscripts()
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116 self.writeOutput()
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117
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118 def compareToAnnotation(self):
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119 transcriptListComparator = TranscriptListsComparator(None, self.verbosity)
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120 transcriptListComparator.setSplitDifference(self.split)
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121 transcriptListComparator.setInputTranscriptContainer(transcriptListComparator.QUERY, self.annotationParser)
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122 transcriptListComparator.setInputTranscriptContainer(transcriptListComparator.REFERENCE, self.referenceParser)
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123 transcriptListComparator.setOutputWriter(self.writer)
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124 transcriptListComparator.getDifferenceTranscriptList()
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125
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126 def run(self):
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127 if self.referenceParser != None:
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128 self.compareToAnnotation()
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129 else:
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130 self.compareToSequence()
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131
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132
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133 if __name__ == "__main__":
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134
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135 # parse command line
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136 description = "Get Difference v1.0.1: Get all the regions of the genome, except the one given or get all the elements from the first set which does not ovelap with the second set (at the nucleotide level). [Category: Data Comparison]"
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137
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138 parser = OptionParser(description = description)
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139 parser.add_option("-i", "--input1", dest="inputFileName1", action="store", type="string", help="input file [compulsory] [format: file in transcript format given by -f]")
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140 parser.add_option("-f", "--format1", dest="format1", action="store", type="string", help="format [compulsory] [format: transcript file format]")
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141 parser.add_option("-j", "--input2", dest="inputFileName2", action="store", default=None, type="string", help="reference file [format: file in transcript format given by -g]")
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142 parser.add_option("-g", "--format2", dest="format2", action="store", default=None, type="string", help="format of the reference file [format: transcript file format]")
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143 parser.add_option("-s", "--sequence", dest="sequenceFileName", action="store", default=None, type="string", help="sequence file [format: file in FASTA format]")
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144 parser.add_option("-p", "--split", dest="split", action="store_true", default=False, help="when comparing to a set of genomic coordinates, do not join [format: boolean] [default: False")
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145 parser.add_option("-o", "--output", dest="outputFileName", action="store", type="string", help="output file [format: output file in GFF3 format]")
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146 parser.add_option("-v", "--verbosity", dest="verbosity", action="store", default=1, type="int", help="trace level [format: int]")
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147 (options, args) = parser.parse_args()
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148
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149 getter = DifferenceGetter(options.verbosity)
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150 getter.setSplit(options.split)
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151 getter.setAnnotationFile(options.inputFileName1, options.format1)
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152 getter.setSequenceFile(options.sequenceFileName)
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153 getter.setReferenceFile(options.inputFileName2, options.format2)
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154 getter.setOutputFile(options.outputFileName)
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155 getter.run()