Mercurial > repos > urgi-team > teiso
diff TEisotools-1.0/commons/core/seq/SequenceModificationsCollection.py @ 6:20ec0d14798e draft
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author | urgi-team |
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date | Wed, 20 Jul 2016 05:00:24 -0400 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/TEisotools-1.0/commons/core/seq/SequenceModificationsCollection.py Wed Jul 20 05:00:24 2016 -0400 @@ -0,0 +1,312 @@ +#!/usr/bin/env python + +# Copyright INRA (Institut National de la Recherche Agronomique) +# http://www.inra.fr +# http://urgi.versailles.inra.fr +# +# 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 +import time +import shutil +from commons.core.seq.BioseqDB import BioseqDB +from commons.core.seq.SequenceModifications import SequenceModifications +from commons.core.checker.RepetException import RepetException + +class SequenceModificationsCollection(object): + + def __init__(self): + self._lSeqModif = [] + + def __str__(self): + result = "" + for iSeqModif in self._lSeqModif: + result += "%s\n" % iSeqModif.__str__() + return result + + def __eq__(self, o): + if type(o) is type(self): + self.sort() + o.sort() + return self._lSeqModif == o._lSeqModif + return False + + def __ne__(self, o): + return not self.__eq__(o) + + def clear(self): + self._lSeqModif = [] + + def add(self, iSeqModif, override = False): + for seqModif in self._lSeqModif: + if seqModif.getOriginalHeader() == iSeqModif.getOriginalHeader(): + if override: + self._lSeqModif.pop(self._lSeqModif.index(seqModif)) + else: + raise RepetException("ERROR: '%s' already in SequenceModificationsCollection" % iSeqModif.getOriginalHeader()) + + self._lSeqModif.append(iSeqModif) + + def get(self, header, mutated = False): + for iSeqModif in self._lSeqModif: + if mutated: + linkToGoodMethod = iSeqModif.getMutatedHeader + else: + linkToGoodMethod = iSeqModif.getOriginalHeader + + if linkToGoodMethod() == header: + return iSeqModif + return None + + def getHeadersList(self, mutated = False): + lHeaders = [] + if mutated: + for iSeqModif in self._lSeqModif: + lHeaders.append(iSeqModif.getMutatedHeader()) + else: + for iSeqModif in self._lSeqModif: + lHeaders.append(iSeqModif.getOriginalHeader()) + lHeaders.sort(key = lambda header: header.lower()) + return lHeaders + + def sort(self): + self._lSeqModif.sort(key = lambda seqMod: seqMod.getOriginalHeader().lower(), reverse = False) + + def writeMutations(self, fileName, outFormat = ""): + self.sort() + with open(fileName, "w") as fH: + if outFormat.lower() in ["gff", "gff3"]: + fH.write("##gff-version 3\n") + for iSeqModif in self._lSeqModif: + for mutation in iSeqModif.getMutations(): + pos = mutation[0] + old = mutation[1] + new = mutation[2] + fH.write("%s\tMutateSequence\tSNP\t%i\t%i\t.\t.\t.\tName=SNP_%i;REF=%s;ALT=%s\n" % (iSeqModif.getOriginalHeader(), pos, pos, pos, old, new)) + else: + fH.write("#Mutations:\n") + fH.write("seqName\tposition\toldNt\tnewNt\n") + for iSeqModif in self._lSeqModif: + for mutation in iSeqModif.getMutations(): + fH.write("%s\t%i\t%s\t%s\n" % (iSeqModif.getOriginalHeader(), mutation[0], mutation[1], mutation[2])) + + def writeInsertions(self, fileName, outFormat = ""): + self.sort() + with open(fileName, "w") as fH: + if outFormat.lower() in ["gff", "gff3"]: + fH.write("##gff-version 3\n") + for iSeqModif in self._lSeqModif: + for iRange in iSeqModif.getInsertions(): + if iRange.getSeqname() != ".": + fH.write("%s\tMutateSequence\tinsertion\t%s\t%s\t.\t.\t.\tName=insertion_%s-%s;insert=%s\n" % (iSeqModif.getOriginalHeader(), iRange.getStart(), iRange.getEnd(), iRange.getStart(), iRange.getEnd(), iRange.getSeqname())) + else: + fH.write("%s\tMutateSequence\tinsertion\t%s\t%s\t.\t.\t.\tName=insertion_%s-%s\n" % (iSeqModif.getOriginalHeader(), iRange.getStart(), iRange.getEnd(), iRange.getStart(), iRange.getEnd())) + else: + fH.write("#Insertions:\n") + fH.write("seqName\tstart\tend\tinsertedSeqName\n") + for iSeqModif in self._lSeqModif: + for iRange in iSeqModif.getInsertions(): + fH.write("%s\t%i\t%i\t%s\n" % (iSeqModif.getOriginalHeader(), iRange.getStart(), iRange.getEnd(), iRange.getSeqname())) + + def writeDeletions(self, fileName, outFormat = ""): + self.sort() + with open(fileName, "w") as fH: + if outFormat.lower() in ["gff", "gff3"]: + fH.write("##gff-version 3\n") + for iSeqModif in self._lSeqModif: + for iRange in iSeqModif.getDeletions(): + fH.write("%s\tMutateSequence\tdeletion\t%s\t%s\t.\t.\t.\tName=deletion_%s-%s\n" % (iSeqModif.getOriginalHeader(), iRange.getStart(), iRange.getEnd(), iRange.getStart(), iRange.getEnd())) + else: + fH.write("#Deletions:\n") + fH.write("seqName\tstart\tend\n") + for iSeqModif in self._lSeqModif: + for iRange in iSeqModif.getDeletions(): + fH.write("%s\t%i\t%i\n" % (iSeqModif.getOriginalHeader(), iRange.getStart(), iRange.getEnd())) + + def write(self, mutationsFileName = "", insertionsFileName = "", deletionsFileName = "", outFormat = ""): + self.sort() + self.writeMutations(mutationsFileName, outFormat) + self.writeInsertions(insertionsFileName, outFormat) + self.writeDeletions(deletionsFileName, outFormat) + + def writeVCF(self, VCFFileName, fastaFileName, software = "MutateSequences"): + self.sort() + tmpVCFFileName = "%s.tmp" % VCFFileName + VCFFH = open(tmpVCFFileName, "w") + VCFFH.write("##fileformat=VCFv4.1\n") + VCFFH.write("##fileDate=%s\n" % time.strftime("%Y%m%d")) + VCFFH.write("##reference=%s\n" % os.path.abspath(fastaFileName)) + VCFFH.write("##INFO=<ID=SVLEN,Number=.,Type=Integer,Description=\"Difference in length between REF and ALT alleles\">\n") + VCFFH.write("##INFO=<ID=SVTYPE,Number=1,Type=String,Description=\"Type of structural variant\">\n") + VCFFH.write("##INFO=<ID=ALTSTART,Number=1,Type=Integer,Description=\"ALT start position on query sequence\">\n") + VCFFH.write("##INFO=<ID=SOFTWARE,Number=1,Type=String,Description=\"Software used to generate this VCF\">\n") + VCFFH.write("##INFO=<ID=INSERTED,Number=1,Type=String,Description=\"Inserted sequence name\">\n") + VCFFH.write("#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\n") + + iBSDB = BioseqDB(fastaFileName) + + for iSeqModif in self._lSeqModif: + for mutation in iSeqModif.getMutations(): + pos = mutation[0] + old = mutation[1] + new = mutation[2] + VCFFH.write("%s\t%s\t.\t%s\t%s\t.\t.\tAN=2;REF=%s;ALT=%s;SOFTWARE=%s\n" % (iSeqModif.getOriginalHeader(), pos, old, new, old, new, software)) + + for insRange in iSeqModif.getInsertions(): + if insRange.getStart() != 1: + refSeq = iBSDB.fetch(iSeqModif.getOriginalHeader()).getNtFromPosition(insRange.getStart() - 1) + altSeq = "." + + INFO = "SVTYPE=INS;AN=2;SVLEN=%d;SOFTWARE=%s" % (insRange.getEnd() - insRange.getStart() + 1, software) + if insRange.getSeqname() != ".": + INFO += ";INSERTED=%s" % insRange.getSeqname() + VCFLine = "%s\t%d\t.\t%s\t%s\t%s\t%s\t%s\n" % (iSeqModif.getOriginalHeader(), insRange.getStart() - 1, refSeq, altSeq, ".", ".", INFO) + + else: + refSeq = iBSDB.fetch(iSeqModif.getOriginalHeader()).getNtFromPosition(insRange.getStart()) + refSeq = "." + altSeq = "." + + INFO = "SVTYPE=INS;AN=2;SVLEN=%d;SOFTWARE=%s" % (insRange.getEnd() - insRange.getStart() + 1, software) + if insRange.getSeqname() != ".": + INFO += ";INSERTED=%s" % insRange.getSeqname() + VCFLine = "%s\t%d\t.\t%s\t%s\t%s\t%s\t%s\n" % (iSeqModif.getOriginalHeader(), insRange.getStart(), refSeq, altSeq, ".", ".", INFO) + + VCFFH.write(VCFLine) + + for delRange in iSeqModif.getDeletions(): + if delRange.getStart() != 1: + refSeq = iBSDB.fetch(iSeqModif.getOriginalHeader()).subseq(delRange.getStart() - 1, delRange.getEnd()).getSequence() + altSeq = refSeq[0] + + INFO = "SVTYPE=DEL;AN=2;SVLEN=-%d;SOFTWARE=%s" % (len(refSeq)-1, software) + VCFLine = "%s\t%d\t.\t%s\t%s\t%s\t%s\t%s\n" % (iSeqModif.getOriginalHeader(), delRange.getStart() - 1, refSeq, altSeq, ".", ".", INFO) + + else: + refSeq = iBSDB.fetch(iSeqModif.getOriginalHeader()).subseq(delRange.getStart(), delRange.getEnd() + 1).getSequence() + altSeq = refSeq[-1] + altSeq = "." + + INFO = "SVTYPE=DEL;AN=2;SVLEN=-%d;SOFTWARE=%s" % (len(refSeq)-1, software) + VCFLine = "%s\t%d\t.\t%s\t%s\t%s\t%s\t%s\n" % (iSeqModif.getOriginalHeader(), delRange.getStart(), refSeq, altSeq, ".", ".", INFO) + + VCFFH.write(VCFLine) + + #This command line can sort this VCF file properly. But can't manage to launch it properly through os.system or subprocess... +# cmd = "(head -n 9 %s && tail -n +10 %s | head -n -1 | sort -f -k1,1 -k2,2n) > %s" % (tmpVCFFileName, tmpVCFFileName, VCFFileName) + shutil.move(tmpVCFFileName, VCFFileName) + + def getCollectionBasedOnMutatedSequence(self): + transformedSeqModifCollec = SequenceModificationsCollection() + + for header in self.getHeadersList(): + currentSeqModif = self.get(header) + + lModifsTuples = [("insertion", iRange) for iRange in currentSeqModif.getInsertions()] + for iRange in currentSeqModif.getDeletions(): + lModifsTuples.append(("deletion", iRange)) + lModifsTuples.sort(key = lambda modifTuple: modifTuple[1].getStart(), reverse = False) + + sumIns = 0 + sumDel = 0 + + iseqModif = SequenceModifications(currentSeqModif.getMutatedHeader(), currentSeqModif.getOriginalHeader()) + for modifTuple in lModifsTuples: + varType = modifTuple[0] + varRange = modifTuple[1] + + if varType == "insertion": + iseqModif.addDeletion(varRange.getStart() + sumIns - sumDel, varRange.getEnd() + sumIns - sumDel) + sumIns += varRange.getLength() + + if varType == "deletion": + iseqModif.addInsertion(varRange.getStart() + sumIns - sumDel, varRange.getEnd() + sumIns - sumDel) + sumDel += varRange.getLength() + + for tSnp in currentSeqModif.getMutations(): + iseqModif.addMutation((tSnp[0], tSnp[2], tSnp[1])) + + iseqModif.sort() + transformedSeqModifCollec.add(iseqModif) + + transformedSeqModifCollec.sort() + + return transformedSeqModifCollec + + def loadSeqModifCollectionFromFiles(self, inInsertionsFileName, inDeletionsFileName, inSNPsFileName, SNPsrate = "0.020000"): + self.clear() + + with open(inInsertionsFileName, "r") as f: + line = f.readline() + while line: + if "seqName" not in line and "#" not in line: + splittedLine = line.split() + seqname = splittedLine[0] + start = int(splittedLine[1]) + end = int(splittedLine[2]) + insertedSeqName = splittedLine[3] + + if self.get(seqname) is None: + self.add(SequenceModifications(seqname)) + self.get(seqname).setMutatedHeader("%s_mutated_%s" % (seqname, SNPsrate)) + self.get(seqname).addInsertion(start, end, insertedSeqName) + line = f.readline() + + with open(inDeletionsFileName, "r") as f: + line = f.readline() + while line: + if "seqName" not in line and "#" not in line: + splittedLine = line.split() + seqname = splittedLine[0] + start = int(splittedLine[1]) + end = int(splittedLine[2]) + + if self.get(seqname) is None: + self.add(SequenceModifications(seqname)) + self.get(seqname).setMutatedHeader("%s_mutated_%s" % (seqname, SNPsrate)) + self.get(seqname).addDeletion(start, end) + line = f.readline() + + with open(inSNPsFileName, "r") as f: + line = f.readline() + while line: + if "seqName" not in line and "#" not in line: + splittedLine = line.split() + seqname = splittedLine[0] + position = int(splittedLine[1]) + oldNt = splittedLine[2] + newNt = splittedLine[3] + + if self.get(seqname) is None: + self.add(SequenceModifications(seqname)) + self.get(seqname).setMutatedHeader("%s_mutated_%s" % (seqname, SNPsrate)) + self.get(seqname).addMutation((position, oldNt, newNt)) + line = f.readline() + + for header in self.getHeadersList(): + self.get(header).sort() + self.sort() \ No newline at end of file