def get_features(self, cluster_number):
left_iv = self.left.iv.copy()
left_iv.strand = "+"
left_feature = HTSeq.GenomicFeature(
"cluster_{0}_left".format(cluster_number), CLUSTER_GFF_TYPE,
left_iv)
left_feature.score = self.left.count
right_iv = self.right.iv.copy()
right_iv.strand = "-"
right_feature = HTSeq.GenomicFeature(
"cluster_{0}_right".format(cluster_number), CLUSTER_GFF_TYPE,
right_iv)
right_feature.score = self.right.count
if self.gap == 0:
gap_iv = HTSeq.GenomicInterval(left_iv.chrom, left_iv.end - 1,
right_iv.start + 1, ".")
else:
# gap_iv = HTSeq.GenomicInterval( left_iv.chrom, left_iv.end+1, right_iv.start-1, "." )
gap_iv = HTSeq.GenomicInterval(left_iv.chrom, left_iv.end,
right_iv.start, ".")
insert_name = "cluster_{0}_insert".format(cluster_number)
insert_feature = HTSeq.GenomicFeature(insert_name, GAP_GFF_TYPE,
gap_iv)
# print dir(insert_feature)
# insert_feature.__setattribute__("length",self.gap)
insert_feature.attr = {"ID": insert_name, "length": self.gap}
return (left_feature, insert_feature, right_feature)
def get_features(self, cluster_number):
singleton_iv = self.singleton.iv.copy()
insert_iv = None
if self.singleton.insertion_side == RIGHT:
singleton_iv.strand = "+"
# insert_iv = HTSeq.GenomicInterval(singleton_iv.chrom, singleton_iv.end+1, singleton_iv.end+1, "." )
insert_iv = HTSeq.GenomicInterval(singleton_iv.chrom,
singleton_iv.end,
singleton_iv.end + 1, ".")
elif self.singleton.insertion_side == LEFT:
singleton_iv.strand = "-"
# insert_iv =HTSeq.GenomicInterval(singleton_iv.chrom, singleton_iv.start-1, singleton_iv.start-1, "." )
insert_iv = HTSeq.GenomicInterval(singleton_iv.chrom,
singleton_iv.start - 1,
singleton_iv.start, ".")
else:
singleton_iv.strand = "."
singleton_feature = HTSeq.GenomicFeature(
"cluster_{0}_singleton".format(cluster_number), CLUSTER_GFF_TYPE,
singleton_iv)
singleton_feature.score = self.singleton.count
feature_list = [singleton_feature]
if insert_iv != None:
insert_feature = HTSeq.GenomicFeature(
"cluster_{0}_junction".format(cluster_number),
SINGLETON_INSERT_GFF_TYPE, insert_iv)
feature_list.append(insert_feature)
return feature_list
def collapseSortedGF(ll):
gf_new = None
l_out = []
i = 0
# loop through list
for feature in ll:
if gf_new is None:
#gf_new = feature
gf_new = HTSeq.GenomicFeature(feature.name, feature.type,
feature.iv.copy())
gf_new.attr = feature.attr.copy()
else:
if feature.iv.overlaps(gf_new.iv):
# features overlap, merge them
gfMerge(gf_new, feature)
else:
# features don't overlap so append the completed "new" feature
# to the output list
l_out.append(gf_new)
# start new "new" feature
#gf_new = feature
gf_new = HTSeq.GenomicFeature(feature.name, feature.type,
feature.iv.copy())
gf_new.attr = feature.attr.copy()
# append final "new" feature
l_out.append(gf_new)
return l_out
def create_peak_gtf(path, exp_design_name, technique, bed_name):
"""
Read all PATH_PEAKS+'/'+exp_design_name+'_'+technique+'_'+Final.txt
Combine peaks
and save to GFF
:param list_technique:
:return:
"""
PATH_ANNOT = path + '/Genome/'
if technique == '' or technique == 'All':
PATH_PEAKS = path + '/PeakDetection/Peaks'
peak_filename = PATH_PEAKS + '/' + exp_design_name + '_' + bed_name + '_Peaks.txt'
gtf_filename = PATH_PEAKS + '/' + exp_design_name + '_' + bed_name + '.gtf'
else:
PATH_PEAKS = path + '/PeakDetection/' + technique + '/'
peak_filename = PATH_PEAKS + '/' + exp_design_name + '_' + technique + '_' + bed_name + '_Peaks.txt'
gtf_filename = PATH_PEAKS + '/' + exp_design_name + '_' + technique + '_' + bed_name + '.gtf'
with open(gtf_filename, 'w') as gtf_file, \
open(peak_filename, 'rU') as peak_file:
csv_peaks = csv.DictReader(peak_file, delimiter='\t')
for row in csv_peaks:
peak = HTSeq.GenomicInterval(row['chromo_peak'],
int(row['begin_peak']),
int(row['end_peak']), ".")
peak_id = row['WindowId']
feature = HTSeq.GenomicFeature(peak_id, 'exon', peak)
#print(feature.get_gff_line().strip() + '; gene_id \"'+peak_id+'\"')
gtf_file.write(feature.get_gff_line().strip() + '; gene_id \"' +
peak_id + '\"' + '\n')
def parseGtf(sz_file, d_g):
##
# variables
szTid = ""
# create reader for GTF
gr = HTSeq.GFF_Reader(sz_file)
# read through the GTF file and load into dict
for feature in gr:
if feature.type == "exon":
szTid = feature.attr['transcript_id']
feature.name = szTid
# add to dict
if szTid not in d_g:
d_g[szTid] = {'exons': [], 'feature': None}
# append current feature to transcript's exon list
# kill strand
feature.iv.strand = "."
d_g[szTid]['exons'].append(feature)
# update feature's genomic interval
if d_g[szTid]['feature'] is None:
d_g[szTid]['feature'] = HTSeq.GenomicFeature(
feature.name, "gene", feature.iv.copy())
d_g[szTid]['feature'].attr = feature.attr.copy()
else:
d_g[szTid]['feature'].iv.start = min(
d_g[szTid]['feature'].iv.start, feature.iv.start)
d_g[szTid]['feature'].iv.end = max(
d_g[szTid]['feature'].iv.end, feature.iv.end)
def _parse_gtf_features(self, transcript_id):
self.feature_set = set()
names = ['chrom','source','feature','start','end','score','strand','frame', 'attribute']
gtf_data = pd.read_table('chr1.gtf', sep='\t', comment='#', names=names)
print 'done reading'
transcript_series = gtf_data['attribute'].apply(self._filter_enst, args=(transcript_id,))
gtf_data = gtf_data.ix[transcript_series]
for r in gtf_data.iterrows():
r = r[1] # iterrows is a tuple of (index, Series)
self.feature_set.add(HTSeq.GenomicFeature(transcript_id, r.feature, HTSeq.GenomicInterval(r.chrom, r.start, r.end, r.strand)))
if aggregateGenes == False:
check_set = set()
for geneID, transcript_id in s:
check_set.add(geneID)
if (len(check_set) > 1):
continue
else:
aggregate_id = gene_id
# Take one of the gene IDs, find the others via gene sets, and
# form the aggregate ID from all of them
else:
assert set(gene_id
for gene_id, transcript_id in s) <= gene_sets[gene_id]
aggregate_id = '+'.join(gene_sets[gene_id])
# Make the feature and store it in 'aggregates'
f = HTSeq.GenomicFeature(aggregate_id, "exonic_part", iv)
f.source = os.path.basename(sys.argv[0])
# f.source = "camara"
f.attr = {}
f.attr['gene_id'] = aggregate_id
transcript_set = set((transcript_id for gene_id, transcript_id in s))
f.attr['transcripts'] = '+'.join(transcript_set)
aggregates[aggregate_id].append(f)
# Step 4: For each aggregate, number the exonic parts
aggregate_features = []
for l in aggregates.values():
for i in range(len(l) - 1):
assert l[i].name == l[i + 1].name, str(l[i + 1]) + " has wrong name"
assert l[i].iv.end <= l[i + 1].iv.start, str(
#Annotate promoters
promoters = []
for iv, s in promoter_part.steps():
if len(s) == 0:
continue
if iv.strand == "+":
new_iv = HTSeq.GenomicInterval(iv.chrom, iv.start - 2000, iv.start,
iv.strand)
else:
new_iv = HTSeq.GenomicInterval(iv.chrom, iv.end, iv.end + 2000,
iv.strand)
for g_id in s:
gene_id = g_id
promoter = HTSeq.GenomicFeature(gene_id, "promoter", new_iv)
promoter.attr = {'gene_id': gene_id}
promoters.append(promoter)
promoters.sort(key=lambda promoter: (promoter.iv.chrom, promoter.iv.start))
fout = open(promoter_file, "w")
for promoter in promoters:
fout.write(promoter.get_gff_line())
fout.close()
#Annotate introns
introns = []
for iv, s in intron_part.steps():
if len(s) == 0:
continue
iv = HTSeq.GenomicInterval(iv.chrom, iv.start, iv.end, iv.strand)
for g_id in s:
def run(args):
exons = collections.defaultdict(
lambda: HTSeq.GenomicArrayOfSets("auto", stranded=True))
gene_region = {}
gene_region_length = collections.Counter()
transcript_region = collections.defaultdict(lambda: dict())
start_codon_region = collections.defaultdict(lambda: dict())
stop_codon_region = collections.defaultdict(lambda: dict())
CDS_region = collections.defaultdict(lambda: dict())
five_UTR_region = collections.defaultdict(lambda: dict())
three_UTR_region = collections.defaultdict(lambda: dict())
# Read features from the input GTF file.
gtffile = HTSeq.GFF_Reader(args.inputfile, end_included=True)
gtffile = filter(
lambda feature: re.search(r'chr[a-zA-Z0-9]+$', feature.iv.chrom),
gtffile)
bad_gene_list = find_bad_genes(gtffile)
logging.info(
"Removing genes with exons in different chromosomes or strands (%i discarded)"
% len(bad_gene_list))
gtffile = filter(
lambda feature: feature.attr['gene_id'] not in bad_gene_list, gtffile)
for feature in gtffile:
if feature.type == "exon":
gene_id = feature.attr["gene_id"]
exons[gene_id][feature.iv] += feature.attr["transcript_id"]
extend_transcript_region(feature, transcript_region)
elif feature.type == "start_codon":
gene_id = feature.attr["gene_id"]
transcript_id = feature.attr["transcript_id"]
start_codon_region[gene_id][transcript_id] = feature.iv
elif feature.type == "stop_codon":
gene_id = feature.attr["gene_id"]
transcript_id = feature.attr["transcript_id"]
stop_codon_region[gene_id][transcript_id] = feature.iv
gene_region = find_gene_region(transcript_region)
gene_region_length = find_gene_region_length(gene_region,
transcript_region)
(CDS_region, five_UTR_region,
three_UTR_region) = find_CDS_and_UTR_region(start_codon_region,
stop_codon_region,
transcript_region)
introns = collections.defaultdict(
lambda: HTSeq.GenomicArrayOfSets("auto", stranded=True))
for gene_id in transcript_region.keys():
for transcript_id in transcript_region[gene_id].keys():
transcript_iv = transcript_region[gene_id][transcript_id]
for iv, step_set in exons[gene_id][transcript_iv].steps():
if transcript_id not in step_set:
introns[gene_id][iv] += transcript_id
# gene_exons_bins redefines the exons in one gene. All exons in the gene region are split into exon bins.
# Each exon bin is a feature (feature type is "exonic_region"), which has attributes: "gene_id" and "transcripts".
# One exon bin is possibly shared by multiple transcripts.
gene_exons_bins = collections.defaultdict(lambda: list())
for gene_id in gene_region.keys():
gene_iv = gene_region[gene_id]
for iv, step_set in exons[gene_id][gene_iv].steps():
transcript_list = list(step_set)
if len(transcript_list) != 0:
feature = HTSeq.GenomicFeature(gene_id, "exonic_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcripts"] = "+".join(transcript_list)
gene_exons_bins[gene_id].append(feature)
if gene_iv.strand == "-":
gene_exons_bins[gene_id] = gene_exons_bins[gene_id][::-1]
# Number the exon bins with attrubute "exonic_region_number" starting from "001".
for exons_bins_list in gene_exons_bins.values():
for i in xrange(len(exons_bins_list)):
exons_bins_list[i].attr["exonic_region_number"] = "%03d" % (i + 1)
# gene_introns_bins redefines the introns in one gene. All introns in the gene region are split into intron bins.
# Each intron bin is a feature (feature type is "intronic_region"), which has attributes: "gene_id" and "transcripts".
# One intron bin is possibly shared by multiple transcripts. If it isn't shared by one transcript, this intron bin
# either overlaps with the exonic region of that transcript or lies outside of the whole region of that transcript.
gene_introns_bins = collections.defaultdict(lambda: list())
for gene_id in gene_region.keys():
gene_iv = gene_region[gene_id]
for iv, step_set in introns[gene_id][gene_iv].steps():
transcript_list = list(step_set)
if len(transcript_list) != 0:
feature = HTSeq.GenomicFeature(gene_id, "intronic_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcripts"] = "+".join(transcript_list)
gene_introns_bins[gene_id].append(feature)
if gene_iv.strand == "-":
gene_introns_bins[gene_id] = gene_introns_bins[gene_id][::-1]
# Number the intron bins with attrubute "intronic_region_number" starting from "001".
for introns_bins_list in gene_introns_bins.values():
for i in xrange(len(introns_bins_list)):
introns_bins_list[i].attr["intronic_region_number"] = "%03d" % (i +
1)
# gene_constitutive_exons_bins defines that kind of exon bins that shared by all the transcripts in one gene.
# Each constitutive exon bin is a feature (feature type is "constitutive_exonic_region"), which has attribute: "gene_id".
logging.info("Generating constitutive exonic region (CER) annotation")
gene_constitutive_exons_bins = collections.defaultdict(lambda: list())
gene_constitutive_exons_start_d = collections.defaultdict(lambda: set())
gene_constitutive_exons_end_d = collections.defaultdict(lambda: set())
gene_constitutive_exons_length = collections.Counter()
gene_constitutive_exons_number = collections.Counter()
for gene_id in gene_region.keys():
transcripts_in_gene = len(transcript_region[gene_id])
gene_iv = gene_region[gene_id]
for iv, step_set in exons[gene_id][gene_iv].steps():
transcript_list = list(step_set)
if len(transcript_list) == transcripts_in_gene:
feature = HTSeq.GenomicFeature(gene_id,
"constitutive_exonic_region",
iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
gene_constitutive_exons_bins[gene_id].append(feature)
gene_constitutive_exons_start_d[gene_id].add(
feature.iv.start_d_as_pos)
gene_constitutive_exons_end_d[gene_id].add(
feature.iv.end_d_as_pos)
gene_constitutive_exons_length[gene_id] += feature.iv.length
gene_constitutive_exons_number[gene_id] += 1
if gene_iv.strand == "-":
gene_constitutive_exons_bins[
gene_id] = gene_constitutive_exons_bins[gene_id][::-1]
for constitutive_exons_bins_list in gene_constitutive_exons_bins.values():
for i in xrange(len(constitutive_exons_bins_list)):
constitutive_exons_bins_list[i].attr[
"constitutive_exonic_region_number"] = "%03d" % (i + 1)
# gene_constitutive_introns_bins defines that kind of intron bins that shared by all the transcripts in one gene.
# Each constitutive intron bin is a feature (feature type is "constitutive_intronic_region"), which has attribute: "gene_id".
# For those intron bins in single transcript gene, if the intron bin is in 5' UTR, it will have attribute: "five_UTR_constitutive_intron";
# If the intron bin is in 3' UTR, it will have attribute: "three_UTR_constitutive_intron".
# Didn't define "five_UTR_constitutive_intron" or "three_UTR_constitutive_intron" for intron bins in multiple transcripts gene yet.
logging.info("Generating constitutive intronic region (CIR) annotation")
gene_constitutive_introns_bins = collections.defaultdict(lambda: list())
gene_constitutive_introns_start_d = collections.defaultdict(lambda: set())
gene_constitutive_introns_end_d = collections.defaultdict(lambda: set())
gene_constitutive_introns_length = collections.Counter()
gene_constitutive_introns_number = collections.Counter()
for gene_id in gene_region.keys():
transcripts_in_gene = len(transcript_region[gene_id])
gene_iv = gene_region[gene_id]
exist_UTR_regions = False
if transcripts_in_gene == 1 and gene_id in start_codon_region.keys():
assert len(start_codon_region[gene_id]) == len(
stop_codon_region[gene_id]) == 1
transcript_id = start_codon_region[gene_id].keys()[0]
start_codon_region_iv = start_codon_region[gene_id].values()[0]
stop_codon_region_iv = stop_codon_region[gene_id].values()[0]
(five_UTR_region_iv, three_UTR_region_iv) = find_UTR_region_iv(
start_codon_region_iv, stop_codon_region_iv,
transcript_region[gene_id][transcript_id])
exist_UTR_regions = True
for iv, step_set in introns[gene_id][gene_iv].steps():
transcript_list = list(step_set)
if len(transcript_list) == transcripts_in_gene:
feature = HTSeq.GenomicFeature(gene_id,
"constitutive_intronic_region",
iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
if exist_UTR_regions == True:
if feature.iv.is_contained_in(five_UTR_region_iv):
feature.attr[
"five_UTR_constitutive_intron"] = "five_UTR_constitutive_intron"
elif feature.iv.is_contained_in(three_UTR_region_iv):
feature.attr[
"three_UTR_constitutive_intron"] = "three_UTR_constitutive_intron"
gene_constitutive_introns_bins[gene_id].append(feature)
gene_constitutive_introns_start_d[gene_id].add(
feature.iv.start_d_as_pos)
gene_constitutive_introns_end_d[gene_id].add(
feature.iv.end_d_as_pos)
gene_constitutive_introns_length[gene_id] += feature.iv.length
gene_constitutive_introns_number[gene_id] += 1
if gene_iv.strand == "-":
gene_constitutive_introns_bins[
gene_id] = gene_constitutive_introns_bins[gene_id][::-1]
five_UTR_constitutive_introns = collections.defaultdict(lambda: list())
three_UTR_constitutive_introns = collections.defaultdict(lambda: list())
for constitutive_introns_bins_list in gene_constitutive_introns_bins.values(
):
for i in xrange(len(constitutive_introns_bins_list)):
gene_id = constitutive_introns_bins_list[i].attr["gene_id"]
constitutive_intronic_region_number = constitutive_introns_bins_list[
i].attr["constitutive_intronic_region_number"] = "%03d" % (i +
1)
if "five_UTR_constitutive_intron" in constitutive_introns_bins_list[
i].attr.keys():
five_UTR_constitutive_introns[gene_id].append(
constitutive_intronic_region_number)
elif "three_UTR_constitutive_intron" in constitutive_introns_bins_list[
i].attr.keys():
three_UTR_constitutive_introns[gene_id].append(
constitutive_intronic_region_number)
# gene_constitutive_junction defines that kind of junction positions that join constitutive exon bin and constitutive intron bin in one gene.
# Each constitutive junction is a feature (feature type is "constitutive_junction"), which has attributes: "gene_id", "constitutive_junction_type", "upstream", "downstream".
# attr["constitutive_junction_type"] can be the value: "5'_splice_junction", which means the upstream of the junction position is a constitutive exon bin,
# and the downstream of the junction position is a constitutive intron bin. In this case, attr["upstream"] will be like "constitutive_exonic_region_number 002" (shows exactly which
# constitutive exon bin in the upstream), and similarly for attr["downstream"].
# On the other hand, attr["constitutive_junction_type"] can be the value: "3'_splice_junction"
logging.info("Generating constitutive junctions (CJ) annotation")
gene_constitutive_junction = collections.defaultdict(lambda: list())
for gene_id in gene_constitutive_exons_start_d.keys():
if gene_id in gene_constitutive_introns_start_d.keys():
gene_constitutive_junction_from_exon_to_intron_set = gene_constitutive_exons_end_d[
gene_id] & gene_constitutive_introns_start_d[gene_id]
for gene_constitutive_junction_pos in gene_constitutive_junction_from_exon_to_intron_set:
feature = HTSeq.GenomicFeature(gene_id,
"constitutive_junction",
gene_constitutive_junction_pos)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
from_region_number = find_region_number(
gene_constitutive_junction_pos,
gene_constitutive_exons_bins[gene_id], "end_d_as_pos")
feature.attr[
"upstream"] = "constitutive_exonic_region_number " + from_region_number
to_region_number, index = find_region_number_and_index(
gene_constitutive_junction_pos,
gene_constitutive_introns_bins[gene_id], "start_d_as_pos")
feature.attr[
"downstream"] = "constitutive_intronic_region_number " + to_region_number
feature.attr[
"constitutive_junction_type"] = "5'_splice_junction"
gene_constitutive_junction[gene_id].append((feature, index))
gene_constitutive_junction_from_intron_to_exon_set = gene_constitutive_exons_start_d[
gene_id] & gene_constitutive_introns_end_d[gene_id]
for gene_constitutive_junction_pos in gene_constitutive_junction_from_intron_to_exon_set:
feature = HTSeq.GenomicFeature(gene_id,
"constitutive_junction",
gene_constitutive_junction_pos)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
from_region_number, index = find_region_number_and_index(
gene_constitutive_junction_pos,
gene_constitutive_introns_bins[gene_id], "end_d_as_pos")
feature.attr[
"upstream"] = "constitutive_intronic_region_number " + from_region_number
to_region_number = find_region_number(
gene_constitutive_junction_pos,
gene_constitutive_exons_bins[gene_id], "start_d_as_pos")
feature.attr[
"downstream"] = "constitutive_exonic_region_number " + to_region_number
feature.attr[
"constitutive_junction_type"] = "3'_splice_junction"
gene_constitutive_junction[gene_id].append((feature, index))
if len(gene_constitutive_junction[gene_id]) > 0:
gene_strand = gene_constitutive_junction[gene_id][0][0].iv.strand
if gene_strand == "+":
gene_constitutive_junction[gene_id].sort(
key=lambda f: (f[0].iv.chrom, f[0].iv.start))
else:
gene_constitutive_junction[gene_id].sort(
key=lambda f: (f[0].iv.chrom, -f[0].iv.start))
for gene_constitutive_junction_list in gene_constitutive_junction.values():
for i in xrange(len(gene_constitutive_junction_list)):
gene_constitutive_junction_list[i][0].attr[
"constitutive_junction_number"] = "%03d" % (i + 1)
feature = gene_constitutive_junction_list[i][0]
gene_id = feature.attr["gene_id"]
constitutive_junction_type = feature.attr[
"constitutive_junction_type"]
if constitutive_junction_type == "5'_splice_junction":
index = gene_constitutive_junction_list[i][1]
gene_constitutive_introns_bins[gene_id][index].attr[
"upstream_constitutive_junction_number"] = "%03d" % (i + 1)
elif constitutive_junction_type == "3'_splice_junction":
index = gene_constitutive_junction_list[i][1]
gene_constitutive_introns_bins[gene_id][index].attr[
"downstream_constitutive_junction_number"] = "%03d" % (i +
1)
# gene_region_features defines a feature for each gene that summarize some key info. feature iv is the gene region.
# Feature type is "gene_region". Each feature has attributes: "gene_id", "transcripts_in_gene" (count how many transcripts in this gene),
# "gene_region_length", "constitutive_exonic_region_length", "constitutive_intronic_region_length".
# For single transcript gene, if any of constitutive intron bins in 5' UTR, it will have attribute "five_UTR_constitutive_introns"
# (value would be like "001,002", list the region numbers); similarly for 3' UTR.
gene_region_features = []
for gene_id in gene_region.keys():
iv = gene_region[gene_id]
feature = HTSeq.GenomicFeature(gene_id, "gene_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcripts_in_gene"] = len(transcript_region[gene_id])
feature.attr["gene_region_length"] = gene_region_length[gene_id]
feature.attr[
"constitutive_exonic_region_length"] = gene_constitutive_exons_length[
gene_id]
feature.attr[
"constitutive_intronic_region_length"] = gene_constitutive_introns_length[
gene_id]
feature.attr[
"constitutive_exonic_region_number"] = gene_constitutive_exons_number[
gene_id]
feature.attr[
"constitutive_intronic_region_number"] = gene_constitutive_introns_number[
gene_id]
if gene_id in five_UTR_constitutive_introns.keys():
feature.attr["five_UTR_constitutive_introns"] = ",".join(
five_UTR_constitutive_introns[gene_id])
if gene_id in three_UTR_constitutive_introns.keys():
feature.attr["three_UTR_constitutive_introns"] = ",".join(
three_UTR_constitutive_introns[gene_id])
gene_region_features.append(feature)
gene_region_features.sort(key=lambda f: (f.iv.chrom, f.iv.start))
# transcript_region_features defines a feature for each transcript. feature iv is the transcript region.
# Feature type is "transcript_region". Each feature has attributes: "gene_id", "transcript_id".
transcript_region_features = collections.defaultdict(lambda: list())
for gene_id in transcript_region.keys():
for transcript_id in transcript_region[gene_id].keys():
iv = transcript_region[gene_id][transcript_id]
feature = HTSeq.GenomicFeature(gene_id, "transcript_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcript_id"] = transcript_id
transcript_region_features[gene_id].append(feature)
CDS_region_features = collections.defaultdict(lambda: list())
for gene_id in CDS_region.keys():
for transcript_id in CDS_region[gene_id].keys():
iv = CDS_region[gene_id][transcript_id]
feature = HTSeq.GenomicFeature(gene_id, "CDS_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcript_id"] = transcript_id
CDS_region_features[gene_id].append(feature)
five_UTR_region_features = collections.defaultdict(lambda: list())
for gene_id in five_UTR_region.keys():
for transcript_id in five_UTR_region[gene_id].keys():
iv = five_UTR_region[gene_id][transcript_id]
feature = HTSeq.GenomicFeature(gene_id, "five_UTR_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcript_id"] = transcript_id
five_UTR_region_features[gene_id].append(feature)
three_UTR_region_features = collections.defaultdict(lambda: list())
for gene_id in three_UTR_region.keys():
for transcript_id in three_UTR_region[gene_id].keys():
iv = three_UTR_region[gene_id][transcript_id]
feature = HTSeq.GenomicFeature(gene_id, "three_UTR_region", iv)
feature.source = "IR_annotation"
feature.attr = {}
feature.attr["gene_id"] = gene_id
feature.attr["transcript_id"] = transcript_id
three_UTR_region_features[gene_id].append(feature)
# Write all newly defined features into new gtf annotation file.
logging.info("Writing annotation to file: %s" %
os.path.join(args.outdir, args.annofile))
f = open(os.path.join(args.outdir, args.annofile), "w")
for gene_region_feature in gene_region_features:
f.write(gene_region_feature.get_gff_line())
gene_id = gene_region_feature.attr["gene_id"]
for feature in transcript_region_features[gene_id]:
f.write(feature.get_gff_line())
for feature in CDS_region_features[gene_id]:
f.write(feature.get_gff_line())
for feature in five_UTR_region_features[gene_id]:
f.write(feature.get_gff_line())
for feature in three_UTR_region_features[gene_id]:
f.write(feature.get_gff_line())
for feature in gene_exons_bins[gene_id]:
f.write(feature.get_gff_line())
for feature in gene_introns_bins[gene_id]:
f.write(feature.get_gff_line())
for feature in gene_constitutive_exons_bins[gene_id]:
f.write(feature.get_gff_line())
for feature in gene_constitutive_introns_bins[gene_id]:
f.write(feature.get_gff_line())
for feature in [
item[0] for item in gene_constitutive_junction[gene_id]
]:
f.write(feature.get_gff_line())
f.close()
def create_sliding_exon_window_GTF(windowSize):
overlap = windowSize / 2
gtf_file = HTSeq.GFF_Reader(
PATH_ANNOT + "/gencodeVM13/gencode.vM13.annotation.exon.gtf",
end_included=True)
windows = HTSeq.GenomicArrayOfSets("auto", stranded=True)
transcriptID = 1
with open(PATH_ANNOT + "/gencodeVM13/gencode.vM13.exon.slidingwindow.gtf",
"w") as slidingGTF:
for feature in gtf_file:
if feature.type == 'exon':
interval = feature.iv
transcriptID += 1
if transcriptID % 1000 == 0:
print('Gene: ' + str(transcriptID) + '/ 100000')
windowID = 1
if interval.strand == '+':
begin = interval.start_d
end = begin + windowSize
while end < interval.end_d:
window = HTSeq.GenomicInterval(interval.chrom, begin,
end + 1,
interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['transcript_name'] + '_' +
feature.attr['exon_number'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
windowID += 1
#print(featureWindow.get_gff_line())
begin += overlap
end = begin + windowSize
slidingGTF.write(featureWindow.get_gff_line())
end = interval.end_d
window = HTSeq.GenomicInterval(interval.chrom, begin, end,
interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['transcript_name'] + '_' +
feature.attr['exon_number'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
if window.length > 1:
slidingGTF.write(featureWindow.get_gff_line())
else:
#print(str(interval.end_d) + ' ' + str(interval.start_d))
begin = interval.start_d
end = begin - windowSize
while end > interval.end_d:
window = HTSeq.GenomicInterval(interval.chrom, end,
begin + 1,
interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['transcript_name'] + '_' +
feature.attr['exon_number'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
windowID += 1
#print(featureWindow.get_gff_line())
begin -= overlap
end = begin - windowSize
slidingGTF.write(featureWindow.get_gff_line())
end = interval.end_d
window = HTSeq.GenomicInterval(interval.chrom, end + 1,
begin, interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['transcript_name'] + '_' +
feature.attr['exon_number'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
if window.length > 1:
slidingGTF.write(featureWindow.get_gff_line())
def main():
"""Main function."""
optParser = optparse.OptionParser(
usage="python %prog [options] <in.gtf> <out.gff>",
description=(
"Script to prepare annotation for DEXSeq."
"This script takes an annotation file in Ensembl GTF format"
"and outputs a 'flattened' annotation file suitable for use "
"with the count_in_exons.py script "
),
epilog=(
"Written by Simon Anders ([email protected]), European Molecular Biology "
"Laboratory (EMBL). (c) 2010. Released under the terms of the GNU General "
"Public License v3. Part of the 'DEXSeq' package. "
"Modified by Vivek Bhardwaj (just a bit!) to write featurecounts gtf as an option. "
"Modified by Jost Vrabic Koren to work with python 3. "
)
)
optParser.add_option(
"-r", "--aggregate", type="choice", dest="aggregate",
choices=("no", "yes"), default="yes",
help=(
"'yes' or 'no'. Indicates whether two or more genes sharing an exon should be merged"
" into an 'aggregate gene'. If 'no', the exons that can not be assiged to a single gene"
" are ignored."
)
)
# add option for featurecounts output
optParser.add_option("-f", "--featurecountsgtf", type="string", dest="fcgtf", action="store",
help="gtf file to write for featurecounts.")
##
(opts, args) = optParser.parse_args()
if len(args) != 2:
sys.stderr.write("Script to prepare annotation for DEXSeq.\n\n")
sys.stderr.write("Usage: python %s <in.gtf> <out.gff>\n\n" % os.path.basename(sys.argv[0]))
sys.stderr.write("This script takes an annotation file in Ensembl GTF format\n")
sys.stderr.write("and outputs a 'flattened' annotation file suitable for use\n")
sys.stderr.write("with the count_in_exons.py script.\n")
sys.exit(1)
try:
import HTSeq
except ImportError:
sys.stderr.write("Could not import HTSeq. Please install the HTSeq Python framework\n")
sys.stderr.write("available from http://www-huber.embl.de/users/anders/HTSeq\n")
sys.exit(1)
gtf_file = args[0]
out_file = args[1]
aggregateGenes = opts.aggregate == "yes"
# Step 1: Store all exons with their gene and transcript ID
# in a GenomicArrayOfSets
exons = HTSeq.GenomicArrayOfSets("auto", stranded=True)
for f in HTSeq.GFF_Reader(gtf_file):
if f.type != "exon":
continue
f.attr['gene_id'] = f.attr['gene_id'].replace(":", "_")
exons[f.iv] += (f.attr['gene_id'], f.attr['transcript_id'])
# Step 2: Form sets of overlapping genes
# We produce the dict 'gene_sets', whose values are sets of gene IDs. Each set
# contains IDs of genes that overlap, i.e., share bases (on the same strand).
# The keys of 'gene_sets' are the IDs of all genes, and each key refers to
# the set that contains the gene.
# Each gene set forms an 'aggregate gene'.
if aggregateGenes == True:
gene_sets = collections.defaultdict(lambda: set())
for iv, s in exons.steps():
# For each step, make a set, 'full_set' of all the gene IDs occuring
# in the present step, and also add all those gene IDs, whch have been
# seen earlier to co-occur with each of the currently present gene IDs.
full_set = set()
for gene_id, transcript_id in s:
full_set.add(gene_id)
full_set |= gene_sets[gene_id]
# Make sure that all genes that are now in full_set get associated
# with full_set, i.e., get to know about their new partners
for gene_id in full_set:
assert gene_sets[gene_id] <= full_set
gene_sets[gene_id] = full_set
# Step 3: Go through the steps again to get the exonic sections. Each step
# becomes an 'exonic part'. The exonic part is associated with an
# aggregate gene, i.e., a gene set as determined in the previous step,
# and a transcript set, containing all transcripts that occur in the step.
# The results are stored in the dict 'aggregates', which contains, for each
# aggregate ID, a list of all its exonic_part features.
aggregates = collections.defaultdict(lambda: list())
for iv, s in exons.steps():
# Skip empty steps
if len(s) == 0:
continue
gene_id = list(s)[0][0]
## if aggregateGenes=FALSE, ignore the exons associated to more than one gene ID
if aggregateGenes == False:
check_set = set()
for geneID, transcript_id in s:
check_set.add(geneID)
if len(check_set) > 1:
continue
else:
aggregate_id = gene_id
# Take one of the gene IDs, find the others via gene sets, and
# form the aggregate ID from all of them
else:
assert set(gene_id for gene_id, transcript_id in s) <= gene_sets[gene_id]
aggregate_id = '+'.join(gene_sets[gene_id])
# Make the feature and store it in 'aggregates'
f = HTSeq.GenomicFeature(aggregate_id, "exonic_part", iv)
f.source = os.path.basename(sys.argv[0])
# f.source = "camara"
f.attr = {}
f.attr['gene_id'] = aggregate_id
transcript_set = set((transcript_id for gene_id, transcript_id in s))
f.attr['transcripts'] = '+'.join(transcript_set)
aggregates[aggregate_id].append(f)
# Step 4: For each aggregate, number the exonic parts
aggregate_features = []
for l in aggregates.values():
for i in range(len(l)-1):
assert l[i].name == l[i+1].name, str(l[i+1]) + " has wrong name"
assert l[i].iv.end <= l[i+1].iv.start, str(l[i+1]) + " starts too early"
if l[i].iv.chrom != l[i+1].iv.chrom:
raise ValueError(
"Same name found on two chromosomes: %s, %s" % (str(l[i]), str(l[i+1]))
)
if l[i].iv.strand != l[i+1].iv.strand:
raise ValueError(
"Same name found on two strands: %s, %s" % (str(l[i]), str(l[i+1]))
)
aggr_feat = HTSeq.GenomicFeature(
l[0].name, "aggregate_gene",
HTSeq.GenomicInterval(l[0].iv.chrom, l[0].iv.start, l[-1].iv.end, l[0].iv.strand)
)
aggr_feat.source = os.path.basename(sys.argv[0])
aggr_feat.attr = {'gene_id': aggr_feat.name}
for i in range(len(l)):
l[i].attr['exonic_part_number'] = "%03d" % (i+1)
aggregate_features.append(aggr_feat)
# Step 5: Sort the aggregates, then write everything out
aggregate_features.sort(key=lambda f: (f.iv.chrom, f.iv.start))
fout = open(out_file, "w")
for aggr_feat in aggregate_features:
fout.write(aggr_feat.get_gff_line())
for f in aggregates[aggr_feat.name]:
fout.write(f.get_gff_line())
fout.close()
## modify file to print gtf if featurecounts gtf requested
fcountgtf = opts.fcgtf
if fcountgtf:
os.system('sed s/aggregate_gene/gene/g ' + out_file + ' > ' + fcountgtf)
os.system('sed -i s/exonic_part/exon/g ' + fcountgtf)
print("Done!")
else:
print("Done!")
transcript]['gene_id'].iloc[0])
genes = "+".join(genes)
if genes not in gene_id.keys(): #if gene appears once
f.attr['gene_id'] = genes
gene_id[genes] = 1
else: #if gene appears more than once
f.attr['gene_id'] = "__00".join([genes, str(gene_id[genes])])
gene_id[genes] += 1
transcipttogenes_id[transcript_id] = f.attr['gene_id']
else:
f.attr['gene_id'] = transcipttogenes_id[transcript_id]
f.name = f.attr['gene_id']
#Store f as GenomicFeature with new gene_id
feat = HTSeq.GenomicFeature(
f.name, f.type,
HTSeq.GenomicInterval(f.iv.chrom, f.iv.start, f.iv.end, f.iv.strand))
feat.attr = {}
feat.attr['gene_id'] = f.attr['gene_id']
if f.type == "exonic_part":
feat.attr['transcripts'] = transcript_id
feat.attr['exonic_part_number'] = f.attr['exonic_part_number']
all_feat.append(feat)
###Step 5: Sort the aggregates, then write everything out
print("=====> WRITING RESULT TO FILE")
fout = open(out_file, "w")
for feat in all_feat:
fout.write(feat.get_gff_line())
fout.close()
def workflow1(file1, test=None):
"""workflow1: only consider "exon" and "CDS"
:param file1: gtf filename
:returns: None
:rtype: None
"""
transcripts = generate_transcripts(file1, test)
## * ######################### populate bed files: merge the range #########################
for each_trans, feature_list in transcripts.iteritems(): # each_trans are just tids, using id to maintain order
temp = re.split("[:|]",each_trans)
chr_gene_id = "%s:%s" % (temp[0],temp[2])
feature_list.sort() # sorted by start_d
if feature_list['exon'] == [] and feature_list['CDS'] == []:
logging.debug("BAD: {each_trans} was skipped in function workflow1 because of both CDS and exon are missing".format(
**locals()))
continue
ordered_CDS=feature_list['CDS']
if len(ordered_CDS) > 1:
for i in range(1, len(ordered_CDS) + 1):
ordered_CDS[i-1].name = "{each_trans}|CDS.{}".format(i, each_trans = each_trans)
elif len(ordered_CDS) == 1:
ordered_CDS[0].name = "%s|CDS" % each_trans
ordered_exon=feature_list['exon']
## special branch with only CDS but no exon
if len(ordered_exon) == 0:
ordered_exon = ordered_CDS
## change exon name
elif len(ordered_exon) > 1:
for i in range(1, len(ordered_exon) + 1):
ordered_exon[i-1].name = "{each_trans}|exon.{}".format(i, each_trans = each_trans)
else:
ordered_exon[0].name = "%s|exon" % each_trans
## normal branch, ordered_exon is main player
chrom=ordered_exon[0].iv.chrom
strand=ordered_exon[0].iv.strand
biotype = feature_list.biotype() # add tag things here, just "coding", "non_coding" for now
feature_list.tag = "coding" if ordered_CDS != [] else "non_coding"
if biotype:
biotype = "|%s" % ("_".join(biotype),) # biotype should be unique
else:
biotype = ""
## _intron
if len(ordered_exon) == 2:
if strand == "+":
intron = construct_iv(chrom, ordered_exon[0].iv.end, ordered_exon[1].iv.start, strand)
else:
intron = construct_iv(chrom, ordered_exon[1].iv.end, ordered_exon[0].iv.start, strand)
feature_list.append(
HTSeq.GenomicFeature("{each_trans}|intron".format(each_trans = each_trans),
"_intron", intron)
)
elif len(ordered_exon) > 2:
for i in range(1,len(ordered_exon)): # get all introns
if strand == "+":
intron = construct_iv(chrom, ordered_exon[i-1].iv.end, ordered_exon[i].iv.start, strand)
else:
intron = construct_iv(chrom, ordered_exon[i].iv.end, ordered_exon[i-1].iv.start, strand)
feature_list.append(
HTSeq.GenomicFeature("{each_trans}|intron.{}".format(i, each_trans=each_trans),
"_intron", intron))
## gene
if strand == "+":
gene = construct_iv(chrom, ordered_exon[0].iv.start, ordered_exon[-1].iv.end, strand) # gene is an iv
else:
gene = construct_iv(chrom, ordered_exon[-1].iv.start, ordered_exon[0].iv.end, strand)
feature_list.append(
HTSeq.GenomicFeature("{each_trans}{biotype}".format(
each_trans = each_trans,
biotype = biotype), "_transcript", gene)
)
if len(ordered_CDS):
## _utr5
if ordered_exon[0].iv.start_d != ordered_CDS[0].iv.start_d:
if strand == "+":
utr5 = construct_iv(chrom, ordered_exon[0].iv.start, ordered_CDS[0].iv.start, strand) # temporary
else:
if ordered_CDS[0].iv.end > ordered_exon[0].iv.end:
continue
utr5 = construct_iv(chrom, ordered_CDS[0].iv.end, ordered_exon[0].iv.end, strand)
prime5_exons = [x.iv for x in ordered_exon if x.iv.overlaps(utr5)]
if len(prime5_exons) == 1:
feature_list.append(
HTSeq.GenomicFeature(
"{each_trans}|utr5".format(each_trans=each_trans),
"_utr5", utr5))
else:
for i in range(1, len(prime5_exons) + 1):
if i == len(prime5_exons):
if strand == "+":
i_utr5 = construct_iv(chrom, prime5_exons[-1].start, utr5.end, strand)
else:
i_utr5 = construct_iv(chrom, utr5.start, prime5_exons[-1].end, strand)
else:
i_utr5 = prime5_exons[i-1]
feature_list.append(
HTSeq.GenomicFeature(
"{each_trans}|utr5.{}".format(i, each_trans=each_trans),
"_utr5", i_utr5))
## stop_codon and utr3
if ordered_CDS[-1].iv.end_d != ordered_exon[-1].iv.end_d:
## get utr3
if feature_list["stop_codon"] != []:
if abs(ordered_CDS[-1].iv.end_d - ordered_exon[-1].iv.end_d) != 3:
if strand == "+":
utr3 = construct_iv(chrom, ordered_CDS[-1].iv.end + 3, ordered_exon[-1].iv.end, strand)
else:
utr3 = construct_iv(chrom, ordered_exon[-1].iv.start, ordered_CDS[-1].iv.start - 3, strand)
else:
utr3 = False # this is important
else:
if strand == "+":
if ordered_CDS[-1].iv.end > ordered_exon[-1].iv.end:
continue
utr3 = construct_iv(chrom, ordered_CDS[-1].iv.end, ordered_exon[-1].iv.end, strand)
else:
utr3 = construct_iv(chrom, ordered_exon[-1].iv.start, ordered_CDS[-1].iv.start, strand)
if utr3: # 有可能没有utr3
prime3_exons = [x.iv for x in feature_list['exon'] if x.iv.overlaps(utr3)]
if len(prime3_exons) == 1:
feature_list.append(
HTSeq.GenomicFeature(
"{each_trans}|utr3".format(each_trans=each_trans),
"_utr3", utr3
)
)
else:
for i in range(1, len(prime3_exons) + 1):
if i == 1:
if strand == "+":
i_utr3 = construct_iv(chrom, utr3.start, prime3_exons[0].end, strand)
else:
i_utr3 = construct_iv(chrom, prime3_exons[0].start, utr3.end, strand)
else:
i_utr3 = prime3_exons[i-1]
feature_list.append(
HTSeq.GenomicFeature(
"{each_trans}|utr3.{}".format(i, each_trans=each_trans),
"_utr3", i_utr3
)
)
## promoter
if strand == "+":
ps = ordered_exon[0].iv.start - args.pl # promoter start position
if ps <0:
ps = 0
promoter=construct_iv(chrom, ps, ordered_exon[0].iv.start, strand)
else: # if strand == "-"
ps = ordered_exon[0].iv.end + args.pl
# if chrom == 'scaffold_42': ##only for debug
# exit( '%s ' % ordered_exon[0].name)
if ps > chr_lengths[chrom]:
ps = chr_lengths[chrom]
if ordered_exon[0].iv.end > ps:
print ( 'skipping:%s, %s, %s, %s' % (chrom, ordered_exon[0].iv.end, ps, strand), file=sys.stderr )
continue
promoter=construct_iv(chrom, ordered_exon[0].iv.end, ps, strand)
feature_list.append(
HTSeq.GenomicFeature(
"{each_trans}|promoter".format(each_trans=each_trans),
"_promoter", promoter
)
)
## record
genes[chr_gene_id].append(gene) # using chr_gene_id: "chr:gene_id"
## create folders
## write to file
for each_trans, feature_list in transcripts.iteritems():
feature_list.report()
if not args.no_whole_report:
feature_list.whole_report()
## close all fhandlers
for x in fhandlers:
try:
x.close()
except:
print("file handler %s cannot be closed, maybe you have closed it?" % x)
pass
if test:
pdb.set_trace()
## * ################### try to output intergenic region ###################
intergenic_f = open("%s/intergenic.bed" % outdir, "w")
outer_genes = OrderedDict()
for chr_gene_id, gs in genes.iteritems():
chr_id = chr_gene_id.split(":")[0]
gene_id = chr_gene_id.split(":")[1]
if chr_id not in outer_genes:
outer_genes[chr_id] = {}
if len(gs) > 1:
gene = construct_iv(gs[0].chrom, min([x.start for x in gs]),
max([x.end for x in gs]), gs[0].strand) # combine multiple transcripts of the same gene
outer_genes[chr_id][gene_id] = gene
else:
outer_genes[chr_id][gene_id] = gs[0]
for chr_id in outer_genes:
flag = 0
former_g = "" # gene before interval
next_g = "" # gene after interval
for gene_id in sorted(outer_genes[chr_id].keys(), key=lambda x: outer_genes[chr_id][x].start): # super-low efficiency
chr_gene_id = "%s:%s" %(chr_id, gene_id)
gene = outer_genes[chr_id][gene_id]
e = gene.end
s = gene.start
assert s < e, (chr_gene_id, gene, s, e)
if flag == s: # does this can happen?
flag = e
former_g = chr_gene_id
continue
elif flag < s: # normal stuff
next_g = chr_gene_id
_id = former_g + "--" + next_g
inter_g = construct_iv(gene.chrom, flag, s, "+")
intergenic_f.write(str_iv2(inter_g, _id))
flag = e
former_g = chr_gene_id
continue
elif flag >= e:
logging.debug("Former({}) may overlap with gene_id({})".format(former_g, gene_id))
continue
elif flag < e:
flag = e
former_g = chr_gene_id
continue
next_g = ""
_id = former_g + "--" + next_g
logging.debug("{0}({1}) has start of {flag}, end of {2}".format(gene.chrom,
chr_id,
chr_lengths[chr_id],
flag=flag))
inter_g = construct_iv(gene.chrom, flag, chr_lengths[chr_id], "+")
logging.debug("OUTPUT last interval, former is %s" % former_g)
intergenic_f.write(str_iv2(inter_g, _id))
intergenic_f.close()
# aggregate ID, a list of all its exonic_part features.
aggregates = collections.defaultdict(lambda: list())
i = -1
for iv, s in exons.steps():
# Skip omitted steps
i += 1
if exon_omit_list[i]:
continue
# Take one of the gene IDs, find the others via gene sets, and
# form the aggregate ID from all of them
gene_id = list(s)[0][0]
assert set(gene_id for gene_id, transcript_id in s) <= gene_sets[gene_id]
aggregate_id = '+'.join(gene_sets[gene_id])
# Make the feature and store it in 'aggregates'
f = HTSeq.GenomicFeature(aggregate_id, "exonic_part", iv)
f.source = os.path.basename(sys.argv[1])
f.attr = {}
f.attr['gene_id'] = aggregate_id
transcript_set = set((transcript_id for gene_id, transcript_id in s))
f.attr['transcripts'] = '+'.join(transcript_set)
aggregates[aggregate_id].append(f)
# Step 4: For each aggregate, number the exonic parts
aggregate_features = []
for l in aggregates.values():
name = l[0].name
chrom = l[0].iv.chrom
strand = l[0].iv.strand
start = l[0].iv.start
def create_sliding_gene_window_GTF(path_annot, annotation_file):
'''
Prepare window file in GTF for Peak detection
Every overlapping window of 100bp on every gene is calculated
:return:
'''
print('Create ' + annotation_file +
'.gene.slidingwindows.gtf file for Peak detection')
print('Every overlapping window of 100bp on every gene is calculated')
overlap = WINDOW_SIZE / 2
gtf_file = HTSeq.GFF_Reader(path_annot + '/' + annotation_file +
'.annotation.gene.gtf',
end_included=True)
windows = HTSeq.GenomicArrayOfSets("auto", stranded=True)
transcriptID = 1
with open(path_annot + '/' + annotation_file + '.gene.slidingwindows.gtf',
"w") as slidingGTF:
for feature in gtf_file:
interval = feature.iv
transcriptID += 1
if transcriptID % 10000 == 0:
print('Gene: ' + str(transcriptID) + '/ 100000')
windowID = 1
if interval.strand == '+':
begin = interval.start_d
end = begin + WINDOW_SIZE
while end < interval.end_d:
window = HTSeq.GenomicInterval(interval.chrom, begin,
end + 1, interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['gene_id'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
windowID += 1
#print(featureWindow.get_gff_line())
begin += overlap
end = begin + WINDOW_SIZE
slidingGTF.write(featureWindow.get_gff_line())
end = interval.end_d
window = HTSeq.GenomicInterval(interval.chrom, begin, end,
interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['gene_id'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID), 'window',
window)
slidingGTF.write(featureWindow.get_gff_line())
else:
#print(str(interval.end_d) + ' ' + str(interval.start_d))
begin = interval.start_d
end = begin - WINDOW_SIZE
while end > interval.end_d:
window = HTSeq.GenomicInterval(interval.chrom, end,
begin + 1, interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['gene_id'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID),
'window', window)
windowID += 1
#print(featureWindow.get_gff_line())
begin -= overlap
end = begin - WINDOW_SIZE
slidingGTF.write(featureWindow.get_gff_line())
end = interval.end_d
window = HTSeq.GenomicInterval(interval.chrom, end + 1, begin,
interval.strand)
featureWindow = HTSeq.GenomicFeature(
feature.attr['gene_id'] + '_window_' +
feature.attr['gene_type'] + '_' + str(windowID), 'window',
window)
slidingGTF.write(featureWindow.get_gff_line())
