Mercurial > repos > bioit_sciensano > phagetermvirome
view _modules/IData_handling.py @ 1:ee73cdf35532 draft default tip
"planemo upload"
author | bioit_sciensano |
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date | Fri, 11 Mar 2022 16:02:03 +0000 |
parents | 69e8f12c8b31 |
children |
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## @file IData_handling.py # # VL: Gather here the classes and functions useful for handling input data. from __future__ import print_function import gzip from _modules.utilities import reverseComplement,changeCase from time import gmtime, strftime import datetime try: import cPickle as pickle except ImportError: # python 3.x import pickle ## This class encapsulates the reference sequences, the host sequence if any and all useful information about the sequences. # # It is used both for searching the read extracts in the sequences and for exploiting the results class refData: def __init__(self,refseq_list,seed,hostseq): self.refseq_list=refseq_list self.seed=seed self.hostseq=hostseq if hostseq!="": self.refseq_list.insert(0,hostseq) self.nb_sequences=len(refseq_list) def getIdxSeq(self,refseq): idx=-1 found=False for s in self.refseq_list: idx += 1 if s==refseq: found=True break if not found: raise RuntimeError("Couldn't find sequence in list of ref sequences.") return idx def IdxIsHostseq(self,idx_seq): if (((self.hostseq == "") and (idx_seq <= self.nb_sequences - 1)) or ( (self.hostseq != "") and (idx_seq >0))): return False return True def getSeqSizesList(self): seq_sizes_list = [] for seq in self.refseq_list: seq_sizes_list.append(len(seq)) return seq_sizes_list ## Base class for handling read extracts. # # This class should not be used directly. class ReadExtracts: def __init__(self,seed): self.seed = seed self.r_extracts_list = [] self.nb_reads = 0 self.nb_extracts=0 ## Returns the list of read extracts from the loaded dataset, the number of reads and the total number of extracts def getRExtracts(self): return self.r_extracts_list,self.nb_reads,self.nb_extracts ## Class containing all the read extracts (PE reads) that must be mapped against a sequence. class readExtractsPE(ReadExtracts): def __init__(self,seed): self.__init__(seed) def addRead(self, whole_PE1,whole_PE2): self.r_extracts_list.append(whole_PE1[:self.seed]) self.r_extracts_list.append(whole_PE1[-self.seed:]) self.r_extracts_list.append(whole_PE2[:self.seed]) self.r_extracts_list.append(reverseComplement(whole_PE2)[:self.seed]) self.r_extracts_list.append(reverseComplement(whole_PE2)[-self.seed:]) self.nb_reads += 1 self.nb_extracts += 5 # Number of extracts per read: 2 extracts for PE1 and 3 for PE2. ## Class containing all the read extracts (single reads) that must be mapped against a sequence. class readsExtractsS(ReadExtracts): def __init__(self,seed): ReadExtracts.__init__(self,seed) ## Adds a read to the list of extracts # # @param whole_read The read as extracted from the fastq file # @param no_pair This paramenter s only used to make the distinction between Single and paired. # Note VL: I didn't use meta programming here because I thought that it would have a negative impact on performance. # TODO: test it when all the rest works. def addRead(self,whole_read,no_pair=""): read_part = whole_read[:self.seed] self.r_extracts_list.append(read_part) self.r_extracts_list.append(whole_read[-self.seed:]) self.r_extracts_list.append(reverseComplement(whole_read)[:self.seed]) self.r_extracts_list.append(reverseComplement(whole_read)[-self.seed:]) self.nb_reads+=1 self.nb_extracts += 4 ## use objects of this class to store read offset (PE1 and PE2) in files. class ReadInfo: def __init__(self, off_PE1,whole_read,seed,off_PE2=None): self.offset1=off_PE1 self.offset2=off_PE2 self.corlen = len(whole_read) - seed ## Gets the number of reads in the fastq file # def getNbReads(fastq): # with open(fastq) as f: # for i, l in enumerate(f): # pass # nb_r=i+1 # nb_r=nb_r/4 # return nb_r ## loads a chunk of reads for mapping on GPU. # Yields a ReadExtracts object plus a dictionnary of ReadInfo. # keeps in memory the parsing state of the file. # @param ch_size is in number of reads # @reset_ids indicates whether or not we want read index to be reset to 0 at the beginning of each chunk. def getChunk(fastq,seed,paired,ch_siz,reset_ids=True): new_chunk = False d_rinfo=dict() idx_read=0 off2=None filin = open(fastq) line = filin.readline() read_paired="" if paired != "": RE=readExtractsPE(seed) filin_paired = open(paired) line_paired = filin_paired.readline() else: RE=readsExtractsS(seed) start = False num_line=0 while line: # Read sequence read = line.split("\n")[0].split("\r")[0] if paired != "": read_paired = line_paired.split("\n")[0].split("\r")[0] if (read[0] == '@' and num_line%4 == 0): # make sure we don't take into account a quality score instead of a read. start = True off1=filin.tell() line = filin.readline() if paired != "": off2=filin_paired.tell() line_paired = filin_paired.readline() continue if (start == True): start = False readlen = len(read) if readlen < seed: line = filin.readline() if paired !="": line_paired = filin_paired.readline() # also skip PE2 in that case continue RE.addRead(read,read_paired) d_rinfo[idx_read]=ReadInfo(off1,read,seed,off2) if (idx_read>0 and ((idx_read+1)%(ch_siz)==0)): yield RE,d_rinfo if (reset_ids): idx_read=0 new_chunk=True if paired != "": RE = readExtractsPE(seed) else: RE = readsExtractsS(seed) d_rinfo = dict() if not new_chunk: idx_read+=1 else: new_chunk=False line = filin.readline() if paired!="": line_paired = filin_paired.readline() filin.close() if paired !="": filin_paired.close() yield RE, d_rinfo ## dumps a dictionnary of ReadInfo objects indexed on read index. # # @param d_rinfo dictionnary to dump # @param fic filename (incl. full path) where to dump def dump_d_rinfo(d_rinfo,fic): with open(fic, 'wb') as fp: pickle.dump(d_rinfo, fp, protocol=pickle.HIGHEST_PROTOCOL) ## Loads a dictionnary of ReadInfo objects. def load_d_rinfo(fic): with open(fic, 'rb') as fp: d_rinfo = pickle.load(fp) return d_rinfo ## loads all extracts of reads into a list for processing on GPU. # # returns 1 or 2 readExtracts objects plus a dictionnary of ReadInfo. def getAllReads(fastq,seed,paired): d_rinfo=dict() idx_read=0 off2=None filin = open(fastq) line = filin.readline() read_paired="" if paired != "": RE=readExtractsPE(seed) filin_paired = open(paired) line_paired = filin_paired.readline() else: RE=readsExtractsS(seed) start = False num_line=0 while line: # Read sequence read = line.split("\n")[0].split("\r")[0] if paired != "": read_paired = line_paired.split("\n")[0].split("\r")[0] if (read[0] == '@' and num_line%4 == 0): # make sure we don't take into account a quality score instead of a read. start = True off1=filin.tell() line = filin.readline() if paired != "": off2=filin_paired.tell() line_paired = filin_paired.readline() continue if (start == True): start = False readlen = len(read) if readlen < seed: line = filin.readline() if paired !="": line_paired = filin_paired.readline() # also skip PE2 in that case continue RE.addRead(read,read_paired) d_rinfo[idx_read]=ReadInfo(off1,read,seed,off2) idx_read+=1 line = filin.readline() if paired!="": line_paired = filin_paired.readline() filin.close() if paired !="": filin_paired.close() return RE,d_rinfo ## use this class to retrieve reads from fastq file. class ReadGetter: ## constructor # # @param fastq Name of the fastq file that contains the read # @param d_rinfo A dictionnary of ReadInfo objects that contains the offset indicating where the read starts in the file. # @param paired The name of the file containing the PE2 (defaults to ""). def __init__(self,fastq,d_rinfo,paired=""): self.filin=open(fastq) self.d_rinfo=d_rinfo self.paired=paired if paired!="": self.filinp=open(fastq) def getOneRead(self,idx_read): read_paired="" self.filin.seek(self.d_rinfo[idx_read].offset1) read=self.filin.readline() if self.paired!="": self.filinp.seek(self.d_rinfo[idx_read].offset2) read_paired = self.filinp.readline() return read,read_paired ### READS Functions def totReads(filin): """Verify and retrieve the number of reads in the fastq file before alignment""" if filin.endswith('.gz'): filein = gzip.open(filin, 'rb') else: filein = open(filin, 'r') line = 0 while filein.readline(): line += 1 seq = float(round(line / 4)) filein.close() return seq ### SEQUENCE parsing function def genomeFastaRecovery(filin, limit_reference, edge, host_test = 0): """Get genome sequence from fasta file""" print("recovering genome from: ",filin) print(strftime("%a, %d %b %Y %H:%M:%S +0000", gmtime())) if filin == "": return "", "", "" infile = open(filin, 'r') name = [] genome = [] genome_line = "" genome_rejected = 0 for line in infile: if line[0] == ">": if name != []: if len(genome_line) >= limit_reference: genome.append(genome_line[-edge:] + genome_line + genome_line[:edge]) else: genome_rejected += 1 name = name[:-1] genome_line = "" name.append(line[1:].split('\r')[0].split('\n')[0]) else: genome_line += changeCase(line).replace(' ', '').split('\r')[0].split('\n')[0] if len(genome_line) >= limit_reference: genome.append(genome_line[-edge:] + genome_line + genome_line[:edge]) genome_line = "" else: genome_rejected += 1 name = name[:-1] infile.close() if host_test: return "".join(genome) else: return genome, name, genome_rejected close(filin)