Mercurial > repos > galaxyp > retrieve_ensembl_bed
diff bedutil.py @ 0:da1b538b87e5 draft
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/proteogenomics/retrieve_ensembl_bed commit 88cf1e923a8c9e5bc6953ad412d15a7c70f054d1
author | galaxyp |
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date | Mon, 22 Jan 2018 13:13:47 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/bedutil.py Mon Jan 22 13:13:47 2018 -0500 @@ -0,0 +1,515 @@ +#!/usr/bin/env python +""" +# +#------------------------------------------------------------------------------ +# University of Minnesota +# Copyright 2016, Regents of the University of Minnesota +#------------------------------------------------------------------------------ +# Author: +# +# James E Johnson +# +#------------------------------------------------------------------------------ +""" + +from __future__ import print_function + +import sys + +from Bio.Seq import reverse_complement, translate + + +def bed_from_line(line, ensembl=False, seq_column=None): + fields = line.rstrip('\r\n').split('\t') + if len(fields) < 12: + return None + (chrom, chromStart, chromEnd, name, score, strand, + thickStart, thickEnd, itemRgb, + blockCount, blockSizes, blockStarts) = fields[0:12] + bed_entry = BedEntry(chrom=chrom, chromStart=chromStart, chromEnd=chromEnd, + name=name, score=score, strand=strand, + thickStart=thickStart, thickEnd=thickEnd, + itemRgb=itemRgb, + blockCount=blockCount, + blockSizes=blockSizes.rstrip(','), + blockStarts=blockStarts.rstrip(',')) + if seq_column is not None and -len(fields) <= seq_column < len(fields): + bed_entry.seq = fields[seq_column] + if ensembl and len(fields) >= 20: + bed_entry.second_name = fields[12] + bed_entry.cds_start_status = fields[13] + bed_entry.cds_end_status = fields[14] + bed_entry.exon_frames = fields[15].rstrip(',') + bed_entry.biotype = fields[16] + bed_entry.gene_name = fields[17] + bed_entry.second_gene_name = fields[18] + bed_entry.gene_type = fields[19] + return bed_entry + + +def as_int_list(obj): + if obj is None: + return None + if isinstance(obj, list): + return [int(x) for x in obj] + elif isinstance(obj, str): + return [int(x) for x in obj.split(',')] + else: # python2 unicode? + return [int(x) for x in str(obj).split(',')] + + +class BedEntry(object): + def __init__(self, chrom=None, chromStart=None, chromEnd=None, + name=None, score=None, strand=None, + thickStart=None, thickEnd=None, itemRgb=None, + blockCount=None, blockSizes=None, blockStarts=None): + self.chrom = chrom + self.chromStart = int(chromStart) + self.chromEnd = int(chromEnd) + self.name = name + self.score = int(score) if score is not None else 0 + self.strand = '-' if str(strand).startswith('-') else '+' + self.thickStart = int(thickStart) if thickStart else self.chromStart + self.thickEnd = int(thickEnd) if thickEnd else self.chromEnd + self.itemRgb = str(itemRgb) if itemRgb is not None else r'100,100,100' + self.blockCount = int(blockCount) + self.blockSizes = as_int_list(blockSizes) + self.blockStarts = as_int_list(blockStarts) + self.second_name = None + self.cds_start_status = None + self.cds_end_status = None + self.exon_frames = None + self.biotype = None + self.gene_name = None + self.second_gene_name = None + self.gene_type = None + self.seq = None + self.cdna = None + self.pep = None + # T26C + self.aa_change = [] + # p.Trp26Cys g.<pos><ref>><alt> # g.1304573A>G + self.variants = [] + + def __str__(self): + return '%s\t%d\t%d\t%s\t%d\t%s\t%d\t%d\t%s\t%d\t%s\t%s' % ( + self.chrom, self.chromStart, self.chromEnd, + self.name, self.score, self.strand, + self.thickStart, self.thickEnd, str(self.itemRgb), self.blockCount, + ','.join([str(x) for x in self.blockSizes]), + ','.join([str(x) for x in self.blockStarts])) + + def get_splice_junctions(self): + splice_juncs = [] + for i in range(self.blockCount - 1): + splice_junc = "%s:%d_%d"\ + % (self.chrom, + self.chromStart + self.blockSizes[i], + self.chromStart + self.blockStarts[i+1]) + splice_juncs.append(splice_junc) + return splice_juncs + + def get_exon_seqs(self): + if not self.seq: + return None + exons = [] + for i in range(self.blockCount): + exons.append(self.seq[self.blockStarts[i]:self.blockStarts[i] + + self.blockSizes[i]]) + if self.strand == '-': # reverse complement + exons.reverse() + for i, s in enumerate(exons): + exons[i] = reverse_complement(s) + return exons + + def get_spliced_seq(self, strand=None): + if not self.seq: + return None + seq = ''.join(self.get_exon_seqs()) + if strand and self.strand != strand: + seq = reverse_complement(seq) + return seq + + def get_cdna(self): + if not self.cdna: + self.cdna = self.get_spliced_seq() + return self.cdna + + def get_cds(self): + cdna = self.get_cdna() + if cdna: + if self.chromStart == self.thickStart\ + and self.chromEnd == self.thickEnd: + return cdna + pos = [self.cdna_offset_of_pos(self.thickStart), + self.cdna_offset_of_pos(self.thickEnd)] + if 0 <= min(pos) <= max(pos) <= len(cdna): + return cdna[min(pos):max(pos)] + return None + + def set_cds(self, cdna_start, cdna_end): + cdna_len = sum(self.blockSizes) + if 0 <= cdna_start < cdna_end <= cdna_len: + cds_pos = [self.pos_of_cdna_offet(cdna_start), + self.pos_of_cdna_offet(cdna_end)] + if all(cds_pos): + self.thickStart = min(cds_pos) + self.thickEnd = max(cds_pos) + return self + return None + + def trim_cds(self, basepairs): + if self.chromStart <= self.thickStart < self.thickEnd <= self.chromEnd: + cds_pos = [self.cdna_offset_of_pos(self.thickStart), + self.cdna_offset_of_pos(self.thickEnd)] + if basepairs > 0: + return self.set_cds(min(cds_pos) + basepairs, max(cds_pos)) + else: + return self.set_cds(min(cds_pos), max(cds_pos) + basepairs) + return None + + def get_cds_bed(self): + cds_pos = [self.cdna_offset_of_pos(self.thickStart), + self.cdna_offset_of_pos(self.thickEnd)] + return self.trim(min(cds_pos), max(cds_pos)) + + def get_cigar(self): + cigar = '' + r = range(self.blockCount) + xl = None + for x in r: + if xl is not None: + intronSize = abs(self.blockStarts[x] - self.blockSizes[xl] + - self.blockStarts[xl]) + cigar += '%dN' % intronSize + cigar += '%dM' % self.blockSizes[x] + xl = x + return cigar + + def get_cigar_md(self): + cigar = '' + md = '' + r = range(self.blockCount) + xl = None + for x in r: + if xl is not None: + intronSize = abs(self.blockStarts[x] - self.blockSizes[xl] + - self.blockStarts[xl]) + cigar += '%dN' % intronSize + cigar += '%dM' % self.blockSizes[x] + xl = x + md = '%d' % sum(self.blockSizes) + return (cigar, md) + + def get_translation(self, sequence=None): + translation = None + seq = sequence if sequence else self.get_spliced_seq() + if seq: + seqlen = len(seq) / 3 * 3 + if seqlen >= 3: + translation = translate(seq[:seqlen]) + return translation + + def get_translations(self): + translations = [] + seq = self.get_spliced_seq() + if seq: + for i in range(3): + translation = self.get_translation(sequence=seq[i:]) + if translation: + translations.append(translation) + return translations + + def pos_of_cdna_offet(self, offset): + if offset is not None and 0 <= offset < sum(self.blockSizes): + r = list(range(self.blockCount)) + rev = self.strand == '-' + if rev: + r.reverse() + nlen = 0 + for x in r: + if offset < nlen + self.blockSizes[x]: + if rev: + return self.chromStart + self.blockStarts[x]\ + + self.blockSizes[x] - (offset - nlen) + else: + return self.chromStart + self.blockStarts[x]\ + + (offset - nlen) + nlen += self.blockSizes[x] + return None + + def cdna_offset_of_pos(self, pos): + if not self.chromStart <= pos < self.chromEnd: + return -1 + r = list(range(self.blockCount)) + rev = self.strand == '-' + if rev: + r.reverse() + nlen = 0 + for x in r: + bStart = self.chromStart + self.blockStarts[x] + bEnd = bStart + self.blockSizes[x] + if bStart <= pos < bEnd: + return nlen + (bEnd - pos if rev else pos - bStart) + nlen += self.blockSizes[x] + + def apply_variant(self, pos, ref, alt): + pos = int(pos) + if not ref or not alt: + print("variant requires ref and alt sequences", file=sys.stderr) + return + if not self.chromStart <= pos <= self.chromEnd: + print("variant not in entry %s: %s %d < %d < %d" % + (self.name, self.strand, + self.chromStart, pos, self.chromEnd), + file=sys.stderr) + print("%s" % str(self), file=sys.stderr) + return + if len(ref) != len(alt): + print("variant only works for snp: %s %s" % (ref, alt), + file=sys.stderr) + return + if not self.seq: + print("variant entry %s has no seq" % self.name, file=sys.stderr) + return + """ + if self.strand == '-': + ref = reverse_complement(ref) + alt = reverse_complement(alt) + """ + bases = list(self.seq) + offset = pos - self.chromStart + for i in range(len(ref)): + # offset = self.cdna_offset_of_pos(pos+i) + if offset is not None: + bases[offset+i] = alt[i] + else: + print("variant offset %s: %s %d < %d < %d" % + (self.name, self.strand, self.chromStart, + pos+1, self.chromEnd), file=sys.stderr) + print("%s" % str(self), file=sys.stderr) + self.seq = ''.join(bases) + self.variants.append("g.%d%s>%s" % (pos+1, ref, alt)) + + def get_variant_bed(self, pos, ref, alt): + pos = int(pos) + if not ref or not alt: + print("variant requires ref and alt sequences", file=sys.stderr) + return None + if not self.chromStart <= pos <= self.chromEnd: + print("variant not in entry %s: %s %d < %d < %d" % + (self.name, self.strand, + self.chromStart, pos, self.chromEnd), + file=sys.stderr) + print("%s" % str(self), file=sys.stderr) + return None + if not self.seq: + print("variant entry %s has no seq" % self.name, file=sys.stderr) + return None + tbed = BedEntry(chrom=self.chrom, + chromStart=self.chromStart, chromEnd=self.chromEnd, + name=self.name, score=self.score, strand=self.strand, + thickStart=self.chromStart, thickEnd=self.chromEnd, + itemRgb=self.itemRgb, + blockCount=self.blockCount, + blockSizes=self.blockSizes, + blockStarts=self.blockStarts) + bases = list(self.seq) + offset = pos - self.chromStart + tbed.seq = ''.join(bases[:offset] + list(alt) + + bases[offset+len(ref):]) + if len(ref) != len(alt): + diff = len(alt) - len(ref) + rEnd = pos + len(ref) + # need to adjust blocks + # change spans blocks, + for x in range(tbed.blockCount): + bStart = tbed.chromStart + tbed.blockStarts[x] + bEnd = bStart + tbed.blockSizes[x] + # change within a block or extends (last block) + # adjust blocksize + # seq: GGGcatGGG + # ref c alt tag: GGGtagatGGG + # ref cat alt a: GGGaGGG + if bStart <= pos < rEnd < bEnd: + tbed.blockSizes[x] += diff + return tbed + + # (start, end) + def get_subrange(self, tstart, tstop, debug=False): + chromStart = self.chromStart + chromEnd = self.chromEnd + if debug: + print("%s" % (str(self)), file=sys.stderr) + r = list(range(self.blockCount)) + if self.strand == '-': + r.reverse() + bStart = 0 + bEnd = 0 + for x in r: + bEnd = bStart + self.blockSizes[x] + if bStart <= tstart < bEnd: + if self.strand == '+': + chromStart = self.chromStart + self.blockStarts[x] +\ + (tstart - bStart) + else: + chromEnd = self.chromStart + self.blockStarts[x] +\ + self.blockSizes[x] - (tstart - bStart) + if bStart <= tstop < bEnd: + if self.strand == '+': + chromEnd = self.chromStart + self.blockStarts[x] +\ + (tstop - bStart) + else: + chromStart = self.chromStart + self.blockStarts[x] +\ + self.blockSizes[x] - (tstop - bStart) + if debug: + print("%3d %s\t%d\t%d\t%d\t%d\t%d\t%d" % + (x, self.strand, bStart, bEnd, + tstart, tstop, chromStart, chromEnd), file=sys.stderr) + bStart += self.blockSizes[x] + return(chromStart, chromEnd) + + # get the blocks for sub range + def get_blocks(self, chromStart, chromEnd): + tblockCount = 0 + tblockSizes = [] + tblockStarts = [] + for x in range(self.blockCount): + bStart = self.chromStart + self.blockStarts[x] + bEnd = bStart + self.blockSizes[x] + if bStart > chromEnd: + break + if bEnd < chromStart: + continue + cStart = max(chromStart, bStart) + tblockStarts.append(cStart - chromStart) + tblockSizes.append(min(chromEnd, bEnd) - cStart) + tblockCount += 1 + return (tblockCount, tblockSizes, tblockStarts) + + def trim(self, tstart, tstop, debug=False): + (tchromStart, tchromEnd) =\ + self.get_subrange(tstart, tstop, debug=debug) + (tblockCount, tblockSizes, tblockStarts) =\ + self.get_blocks(tchromStart, tchromEnd) + tbed = BedEntry( + chrom=self.chrom, chromStart=tchromStart, chromEnd=tchromEnd, + name=self.name, score=self.score, strand=self.strand, + thickStart=tchromStart, thickEnd=tchromEnd, itemRgb=self.itemRgb, + blockCount=tblockCount, + blockSizes=tblockSizes, blockStarts=tblockStarts) + if self.seq: + ts = tchromStart-self.chromStart + te = tchromEnd - tchromStart + ts + tbed.seq = self.seq[ts:te] + return tbed + + def get_filtered_translations(self, untrimmed=False, filtering=True, + ignore_left_bp=0, ignore_right_bp=0, + debug=False): + translations = [None, None, None] + seq = self.get_spliced_seq() + ignore = (ignore_left_bp if self.strand == '+' + else ignore_right_bp) / 3 + block_sum = sum(self.blockSizes) + exon_sizes = [x for x in self.blockSizes] + if self.strand == '-': + exon_sizes.reverse() + splice_sites = [sum(exon_sizes[:x]) / 3 + for x in range(1, len(exon_sizes))] + if debug: + print("splice_sites: %s" % splice_sites, file=sys.stderr) + junc = splice_sites[0] if len(splice_sites) > 0 else exon_sizes[0] + if seq: + for i in range(3): + translation = self.get_translation(sequence=seq[i:]) + if translation: + tstart = 0 + tstop = len(translation) + offset = (block_sum - i) % 3 + if debug: + print("frame: %d\ttstart: %d tstop: %d " + + "offset: %d\t%s" % + (i, tstart, tstop, offset, translation), + file=sys.stderr) + if not untrimmed: + tstart = translation.rfind('*', 0, junc) + 1 + stop = translation.find('*', junc) + tstop = stop if stop >= 0 else len(translation) + offset = (block_sum - i) % 3 + trimmed = translation[tstart:tstop] + if debug: + print("frame: %d\ttstart: %d tstop: %d " + + "offset: %d\t%s" % + (i, tstart, tstop, offset, trimmed), + file=sys.stderr) + if filtering and tstart > ignore: + continue + # get genomic locations for start and end + if self.strand == '+': + chromStart = self.chromStart + i + (tstart * 3) + chromEnd = self.chromEnd - offset\ + - (len(translation) - tstop) * 3 + else: + chromStart = self.chromStart + offset\ + + (len(translation) - tstop) * 3 + chromEnd = self.chromEnd - i - (tstart * 3) + # get the blocks for this translation + (tblockCount, tblockSizes, tblockStarts) =\ + self.get_blocks(chromStart, chromEnd) + translations[i] = (chromStart, chromEnd, trimmed, + tblockCount, tblockSizes, tblockStarts) + if debug: + print("tblockCount: %d tblockStarts: %s " + + "tblockSizes: %s" % + (tblockCount, tblockStarts, tblockSizes), + file=sys.stderr) + return translations + + def get_seq_id(self, seqtype='unk:unk', reference='', frame=None): + # Ensembl fasta ID format + # >ID SEQTYPE:STATUS LOCATION GENE TRANSCRIPT + # >ENSP00000328693 pep:splice chromosome:NCBI35:1:904515:910768:1\ + # gene:ENSG00000158815:transcript:ENST00000328693\ + # gene_biotype:protein_coding transcript_biotype:protein_coding + frame_name = '' + chromStart = self.chromStart + chromEnd = self.chromEnd + strand = 1 if self.strand == '+' else -1 + if frame is not None: + block_sum = sum(self.blockSizes) + offset = (block_sum - frame) % 3 + frame_name = '_' + str(frame + 1) + if self.strand == '+': + chromStart += frame + chromEnd -= offset + else: + chromStart += offset + chromEnd -= frame + location = "chromosome:%s:%s:%s:%s:%s"\ + % (reference, self.chrom, chromStart, chromEnd, strand) + seq_id = "%s%s %s %s" % (self.name, frame_name, seqtype, location) + return seq_id + + def get_line(self, start_offset=0, end_offset=0): + if start_offset or end_offset: + s_offset = start_offset if start_offset else 0 + e_offset = end_offset if end_offset else 0 + if s_offset > self.chromStart: + s_offset = self.chromStart + chrStart = self.chromStart - s_offset + chrEnd = self.chromEnd + e_offset + blkSizes = self.blockSizes + blkSizes[0] += s_offset + blkSizes[-1] += e_offset + blkStarts = self.blockStarts + for i in range(1, self.blockCount): + blkStarts[i] += s_offset + items = [str(x) for x in [self.chrom, chrStart, chrEnd, self.name, + self.score, self.strand, self.thickStart, + self.thickEnd, self.itemRgb, + self.blockCount, + ','.join([str(x) for x in blkSizes]), + ','.join([str(x) for x in blkStarts])]] + return '\t'.join(items) + '\n' + return self.line