Mercurial > repos > yufei-luo > s_mart
diff smart_toolShed/SMART/Java/Python/CollapseReads.py @ 0:e0f8dcca02ed
Uploaded S-MART tool. A toolbox manages RNA-Seq and ChIP-Seq data.
author | yufei-luo |
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date | Thu, 17 Jan 2013 10:52:14 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/smart_toolShed/SMART/Java/Python/CollapseReads.py Thu Jan 17 10:52:14 2013 -0500 @@ -0,0 +1,174 @@ +#! /usr/bin/env python +# +# Copyright INRA-URGI 2009-2010 +# +# This software is governed by the CeCILL license under French law and +# abiding by the rules of distribution of free software. You can use, +# modify and/ or redistribute the software under the terms of the CeCILL +# license as circulated by CEA, CNRS and INRIA at the following URL +# "http://www.cecill.info". +# +# As a counterpart to the access to the source code and rights to copy, +# modify and redistribute granted by the license, users are provided only +# with a limited warranty and the software's author, the holder of the +# economic rights, and the successive licensors have only limited +# liability. +# +# In this respect, the user's attention is drawn to the risks associated +# with loading, using, modifying and/or developing or reproducing the +# software by the user in light of its specific status of free software, +# that may mean that it is complicated to manipulate, and that also +# therefore means that it is reserved for developers and experienced +# professionals having in-depth computer knowledge. Users are therefore +# encouraged to load and test the software's suitability as regards their +# requirements in conditions enabling the security of their systems and/or +# data to be ensured and, more generally, to use and operate it in the +# same conditions as regards security. +# +# The fact that you are presently reading this means that you have had +# knowledge of the CeCILL license and that you accept its terms. +# +import os +from optparse import OptionParser, OptionGroup +from commons.core.parsing.ParserChooser import ParserChooser +from commons.core.writer.Gff3Writer import Gff3Writer +from SMART.Java.Python.structure.Transcript import Transcript +from SMART.Java.Python.ncList.NCListFilePickle import NCListFileUnpickle +from SMART.Java.Python.ncList.FileSorter import FileSorter +from SMART.Java.Python.misc.Progress import Progress + + +class CollapseReads(object): + """ + Merge two reads if they have exactly the same genomic coordinates + """ + + def __init__(self, verbosity = 0): + self.verbosity = verbosity + self.inputReader = None + self.outputWriter = None + self.strands = True + self.nbRead = 0 + self.nbWritten = 0 + self.nbMerges = 0 + self.splittedFileNames = {} + + def __del__(self): + for fileName in self.splittedFileNames.values(): + os.remove(fileName) + + def close(self): + self.outputWriter.close() + + def setInputFile(self, fileName, format): + parserChooser = ParserChooser(self.verbosity) + parserChooser.findFormat(format, "transcript") + self.parser = parserChooser.getParser(fileName) + self.sortedFileName = "%s_sorted.pkl" % (os.path.splitext(fileName)[0]) + + def setOutputFile(self, fileName): + self.outputWriter = Gff3Writer(fileName, self.verbosity) + + def getNbElements(self): + return self.parser.getNbTranscripts() + + def _sortFile(self): + fs = FileSorter(self.parser, self.verbosity-4) + fs.perChromosome(True) + fs.setOutputFileName(self.sortedFileName) + fs.sort() + self.splittedFileNames = fs.getOutputFileNames() + self.nbElementsPerChromosome = fs.getNbElementsPerChromosome() + self.nbRead = fs.getNbElements() + + def _iterate(self, chromosome): + progress = Progress(self.nbElementsPerChromosome[chromosome], "Checking chromosome %s" % (chromosome), self.verbosity) + transcripts = [] + parser = NCListFileUnpickle(self.splittedFileNames[chromosome], self.verbosity) + for newTranscript in parser.getIterator(): + newTranscripts = [] + for oldTranscript in transcripts: + if self._checkOverlap(newTranscript, oldTranscript): + self._merge(newTranscript, oldTranscript) + elif self._checkPassed(newTranscript, oldTranscript): + self._write(oldTranscript) + else: + newTranscripts.append(oldTranscript) + newTranscripts.append(newTranscript) + transcripts = newTranscripts + progress.inc() + for transcript in transcripts: + self._write(transcript) + progress.done() + + def _merge(self, transcript1, transcript2): + self.nbMerges += 1 + transcript2.setDirection(transcript1.getDirection()) + transcript1.merge(transcript2) + + def _write(self, transcript): + self.nbWritten += 1 + self.outputWriter.addTranscript(transcript) + + def _checkOverlap(self, transcript1, transcript2): + if transcript1.getStart() != transcript2.getStart() or transcript1.getEnd() != transcript2.getEnd(): + return False + return (not self.strands or transcript1.getDirection() == transcript2.getDirection()) + + def _checkPassed(self, transcript1, transcript2): + return (transcript2.getStart() < transcript1.getStart()) + + def collapseChromosome(self, chromosome): + progress = Progress(table.getNbElements(), "Analysing chromosome %s" % (chromosome), self.verbosity) + command = "SELECT * FROM %s ORDER BY start ASC, end DESC" % (table.name) + transcriptStart = None + transcriptEnd = None + transcriptDirection = None + currentTranscript = None + if self.strands: + command += ", direction" + for index, transcript in table.selectTranscripts(command, True): + self.nbRead += 1 + if not self.strands: + transcript.setDirection("+") + if transcriptStart != transcript.getStart() or transcriptEnd != transcript.getEnd() or transcriptDirection != transcript.getDirection(): + self.writeTranscript(currentTranscript) + transcriptStart = transcript.getStart() + transcriptEnd = transcript.getEnd() + transcriptDirection = transcript.getDirection() + currentTranscript = transcript + else: + currentTranscript.setTagValue("nbElements", (currentTranscript.getTagValue("nbElements") + 1) if "nbElements" in currentTranscript.getTagNames() else 1) + progress.inc() + self.writeTranscript(currentTranscript) + progress.done() + + def collapse(self): + self._sortFile() + for chromosome in sorted(self.nbElementsPerChromosome.keys()): + self._iterate(chromosome) + self.outputWriter.close() + if self.verbosity > 1: + print "# reads read: %d" % (self.nbRead) + print "# reads written: %d (%.2f%%)" % (self.nbWritten, float(self.nbWritten) / self.nbRead * 100) + print "# reads merges: %d" % (self.nbMerges) + +if __name__ == "__main__": + + # parse command line + description = "Collapse Reads v1.0.3: Merge two reads if they have exactly the same genomic coordinates. [Category: Merge]" + + parser = OptionParser(description = description) + parser.add_option("-i", "--input", dest="inputFileName", action="store", type="string", help="input file [compulsory] [format: file in mapping format given by -f]") + parser.add_option("-f", "--format", dest="format", action="store", type="string", help="format of the file [compulsory] [format: mapping file format]") + parser.add_option("-o", "--output", dest="outputFileName", action="store", type="string", help="output file [compulsory] [format: output file in GFF3 format]") + parser.add_option("-s", "--strands", dest="strands", action="store_true", default=False, help="merge elements on 2 different strands [format: bool] [default: false]") + parser.add_option("-v", "--verbosity", dest="verbosity", action="store", default=1, type="int", help="trace level [default: 1] [format: int]") + (options, args) = parser.parse_args() + + collapser = CollapseReads(options.verbosity) + collapser.setInputFile(options.inputFileName, options.format) + collapser.setOutputFile(options.outputFileName) + collapser.strands = not options.strands + collapser.collapse() + collapser.close()