def read_file(fn, args):
"""
Read OptimiR file and convert to mirtop GFF format.
Args:
*fn(str)*: file name with isomiR-SEA output information.
*database(str)*: database name.
*args(namedtuple)*: arguments from command line.
See *mirtop.libs.parse.add_subparser_gff()*.
Returns:
*reads (nested dicts)*:gff_list has the format as
defined in *mirtop.gff.body.read()*.
"""
database = args.database
gtf = args.gtf
sep = " " if args.out_format == "gtf" else "="
sample = read_samples(fn)
reads = defaultdict(dict)
logger.debug("OPTIMIR::SAMPLE::%s" % sample)
with open(fn) as handle:
for line in handle:
gff = feature(line)
fixed_line = line
if gff.columns:
if "Variant" not in gff.attributes:
gff.attributes["Variant"] = "NA"
logger.debug("OPTIMIR::Chrom update from %s to %s" %
(gff.columns["chrom"], gff.attributes["Parent"]))
gff.columns["chrom"] = gff.attributes["Parent"].split(",")[0]
fixed_line = gff.paste_columns(sep=sep)
if args.add_extra:
extra = variant_with_nt(fixed_line, args.precursors,
args.matures)
fixed_line = "%s Changes %s;" % (fixed_line, extra)
fixed_line = paste_columns(feature(fixed_line), sep=sep)
counts = gff.attributes["Expression"].split(",")
chrom = gff.columns["chrom"]
start = gff.columns["start"]
if start not in reads[chrom]:
reads[chrom][start] = []
reads[chrom][start].append([
gff.attributes["UID"], gff.columns["chrom"], counts,
sample, fixed_line
])
return reads
def read(fn, args):
"""Read GTF/GFF file and load into annotate, chrom counts, sample, line"""
samples = read_samples(fn)
lines = defaultdict(dict)
sep = " " if args.out_format == "gtf" else "="
corrupted_uid = 0
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
line = paste_columns(feature(line), sep=sep)
gff = feature(line)
cols = gff.columns
attr = gff.attributes
if attr['UID'] and not read_id(attr['UID']):
corrupted_uid += 1
continue
if 'UID' not in attr:
msg = "UID not found."
if 'Read' not in attr:
if not is_sequence(attr['Read']):
msg = msg + " Sequence not valid in Read attribute."
else:
attr['UID'] = make_id(attr['Read'])
if 'sequence' not in attr:
msg = msg + " Sequence not found in sequence attribute."
if not is_sequence(attr['sequence']):
msg = msg + " Sequence not valid in sequence attribute."
else:
attr['UID'] = make_id(attr['Read'])
if 'UID' not in attr:
logger.warning("Line is not a valid GFF3 line: %s" %
line.strip())
logger.warning(msg)
if cols['start'] not in lines[cols['chrom']]:
lines[cols['chrom']][cols['start']] = []
uid = "%s-%s-%s" % (attr['UID'],
attr['Variant'],
attr['Name'])
if args.keep_name:
uid = "%s-%s" % (uid, attr['Read'])
lines[cols['chrom']][cols['start']].append(
[uid,
cols['chrom'],
attr['Expression'].strip().split(","),
samples,
line.strip()])
logger.info("Lines skipped due to corrupted UID: %s" % corrupted_uid)
return lines
def _convert_file(gff, args):
sep = "\t"
precursors = fasta.read_precursor(args.hairpin, args.sps)
matures = mapper.read_gtf_to_precursor(args.gtf)
variant_header = sep.join(['mism', 'add', 't5', 't3'])
gff_file = open(gff, 'r')
out_file = os.path.join(args.out, "%s_rawData.tsv" % os.path.splitext(os.path.basename(gff))[0])
missing_parent = 0
missing_mirna = 0
unvalid_uid = 0
with open(out_file, 'w') as outh:
for samples_line in gff_file:
if samples_line.startswith("## COLDATA:"):
samples = sep.join(samples_line.strip().split("COLDATA:")[1].strip().split(","))
header = sep.join(['seq', 'mir',
variant_header, samples])
print(header, file=outh)
break
for mirna_line in gff_file:
gff = feature(mirna_line)
attr = gff.attributes
UID = attr["UID"]
Read = attr["Read"]
mirna = attr["Name"]
parent = attr["Parent"]
variant = attr["Variant"]
try:
Read = read_id(UID)
except KeyError:
unvalid_uid += 1
continue
expression = sep.join(attr["Expression"].strip().split(","))
cols_variants = sep.join(_expand(variant))
logger.debug("COUNTS::Read:%s" % Read)
logger.debug("COUNTS::EXTRA:%s" % variant)
if parent not in precursors:
missing_parent += 1
continue
if mirna not in matures[parent]:
missing_mirna += 1
continue
extra = variant_with_nt(mirna_line, precursors, matures)
if extra == "Invalid":
continue
logger.debug("COUNTS::EXTRA:%s" % extra)
cols_variants = sep.join(_expand(extra, True))
summary = sep.join([Read, mirna,
cols_variants, expression])
logger.debug(summary)
print(summary, file=outh)
gff_file.close()
logger.info("Missing Parents in hairpin file: %s" % missing_parent)
logger.info("Missing MiRNAs in GFF file: %s" % missing_mirna)
logger.info("Non valid UID: %s" % unvalid_uid)
logger.info("Output file is at %s" % out_file)
def test_alignment(self):
"""testing alignments function"""
from mirtop.bam import bam
from mirtop.gff.classgff import feature
fns = {
"let7-last1D.sam": {
56: "iso_add3p:1,iso_snv"
},
"let7-1D.sam": {
5: "iso_snv,iso_3p:-5"
},
"let7-last7M1I.sam": {
5: "iso_add3p:1,iso_snv_seed"
},
"let7-middle1D.sam": {
5: "iso_snv_central_supp,iso_3p:-2"
},
"let7-perfect.sam": {
5: "NA"
},
"let7-triming.sam": {
5: "iso_3p:+2",
4: "iso_5p:-1",
6: "iso_5p:+1,iso_3p:-3"
}
}
#import pdb; pdb.set_trace()
for fn in fns:
gff = annotate("data/aligments/%s" % fn, bam.read_bam)
for pos in gff['hsa-let-7a-1']:
f = feature(gff['hsa-let-7a-1'][pos][0][4])
if not set(f.attributes['Variant'].split(",")) == set(
fns[fn][pos].split(",")):
raise ValueError("Error in %s" % fn)
def test_class(self):
"""Test class to read GFF line"""
from mirtop.gff.classgff import feature
gff = feature("hsa-let-7a-5p\tmiRBasev21\tisomiR\t4\t25\t0\t+\t.\t"
"Read hsa-let-7a-1_hsa-let-7a-5p_5:26_-1:-1_mut:"
"null_add:null_x861; UID bhJJ5WJL2;"
" Name hsa-let-7a-5p; Parent hsa-let-7a-1;"
" Variant iso_5p:+1,iso_3p:-1; Cigar 22M;"
" Expression 861; Filter Pass; Hits 1;")
print(gff.columns)
print(gff.attributes)
def _process(fn, out_dir):
if out_dir:
out_fasta = os.path.join(
out_dir, "%s.fasta" % os.path.splitext(os.path.basename(fn))[0])
outh = sys.stdout if not out_dir else open(out_fasta, 'w')
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
gff = feature(line)
attr = gff.attributes
read = read_id(attr["UID"])
print((">{0}\n{1}").format(attr["UID"], read), file=outh)
def _read_file(fn, precursors, matures, out_dir):
samples = read_samples(fn)
for sample in samples:
with open(os.path.join(out_dir, "%s.mirna" % sample), 'w') as outh:
print("\t".join([
"seq", "name", "freq", "mir", "start", "end", "mism", "add",
"t5", "t3", "s5", "s3", "DB", "precursor", "ambiguity"
]),
file=outh)
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
gff = feature(line)
cols = gff.columns
attr = gff.attributes
read = read_id(attr["UID"])
t5 = variant_to_5p(precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]],
attr["Variant"])
t3 = variant_to_3p(precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]],
attr["Variant"])
add = variant_to_add(read, attr["Variant"])
mature_sequence = get_mature_sequence(
precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]])
mm = align_from_variants(read, mature_sequence, attr["Variant"])
if len(mm) > 1:
continue
elif len(mm) == 1:
mm = "".join(list(map(str, mm[0])))
else:
mm = "0"
hit = attr["Hits"] if "Hits" in attr else "1"
logger.debug("exporter::isomir::decode %s" %
[attr["Variant"], t5, t3, add, mm])
# Error if attr["Read"] doesn't exist
# print(cols)
line = [
read, attr["Read"], "0", attr["Name"], cols['source'],
cols['type'], mm, add, t5, t3, "NA", "NA", "miRNA",
attr["Parent"], hit
]
for sample, counts in zip(samples, attr["Expression"].split(",")):
with open(os.path.join(out_dir, "%s.mirna" % sample),
'a') as outh:
line[2] = counts
print("\t".join(line), file=outh)
def lift_to_genome(line, mapper):
"""
Function to get a class of type feature from classgff.py
and map the precursors coordinates to the genomic coordinates
Args:
*line(str)*: string GFF line.
*mapper(dict)*: dict with mirna-precursor-genomic coordinas from
mirna.mapper.read_gtf_to_mirna function.
Returns:
*(line)*: string with GFF line with updated chr, star, end, strand
"""
features = feature(line)
features.attributes["Variant"]
chr, start, end, strand, id = mapper[features.attributes["Name"]][features.attributes["Parent"]]
logger.debug("LIFT2GENOME:: %s of %s found in %s(%s) " % (features.attributes["Name"],
features.attributes["Parent"],
chr, strand))
nstart = start
nend = end
variants = read_variant(features.attributes["Variant"])
logger.debug("LIFT2GENOME:: variants %s " % (features.attributes["Variant"]))
if 'iso_5p' in variants:
if strand == "+":
nstart = start + variants['iso_5p']
else:
nend = end - variants['iso_5p']
if 'iso_3p' in variants:
if strand == "+":
nend = end + variants['iso_3p']
else:
nstart = start - variants['iso_3p']
if 'iso_add3p' in variants:
if strand == "+":
nend = nend + variants['iso_add3p']
else:
nstart = nstart - variants['iso_add3p']
logger.debug("LIFT2GENOME:: start %s to %s | end %s to %s " % (start, nstart, end, nend))
features.columns['chrom'] = chr
features.columns['start'] = str(start)
features.columns['end'] = str(end)
features.columns['strand'] = strand
return features.paste_columns()
def create_line(read, name, database, args):
sep = " " if args.out_format == "gtf" else "="
if args.add_extra:
precursors = args.precursors
matures = args.matures
for (ps, iso) in read.precursors.items():
p = list(ps)[0]
if not iso.mirna:
continue
chrom = p
seq = read.sequence
seq_name = seq if not args.keep_name else name
if iso.get_score(len(seq)) < 1:
continue
if iso.subs:
iso.subs = [] if "N" in iso.subs[0] else iso.subs
idseq = read.idseq
source = "ref_miRNA" if not iso.is_iso() else "isomiR"
strand = iso.strand
start, end = iso.start, iso.end
score = iso.map_score
mirName = iso.mirna
preName = p
Variant = iso.formatGFF()
Cigar = iso.cigar
counts = read.counts
Filter = iso.filter
annotation = "%s.%s.%s" % (chrom, idseq, seq_name)
# This get correctly formated with paste_columns below
attrb = ("Read {seq_name};UID {idseq};Name {mirName};"
"Parent {preName};"
"Variant {Variant};Cigar {Cigar};"
"Expression {counts};"
"Filter {Filter};").format(**locals())
line = ("{chrom}\t{database}\t{source}\t{start}\t{end}"
"\t{score}\t{strand}\t.\t{attrb}").format(**locals())
logger.debug("GFF::%s" % line)
if args.add_extra:
extra = variant_with_nt(line, precursors, matures)
line = "%s Changes %s;" % (line, extra)
line = feature(line).paste_columns(sep)
return line
def read_reference(fn):
"""Read GFF into UID:Variant
Args:
*fn (str)*: GFF file.
Returns:
*srna (dict)*: dict with >>> {'UID': 'iso_snp:-2,...'}
"""
srna = dict()
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
gff = feature(line)
attr = gff.attributes
srna[attr['UID']] = [_simplify(attr['Variant']), attr]
return srna
def to10to11(gff_line):
gff_line = gff_line.replace("_snp", "_snv")
gff_line = gff_line.replace("_add", "_add3p")
features = feature(gff_line)
if "iso_5p" in features.attributes["Variant"]:
variants = features.attributes["Variant"].split(",")
iso_5p = [v.split(":") for v in variants if v.startswith("iso_5p")]
iso_5p = -1 * int(iso_5p[0][1])
if iso_5p > 0:
iso_5p = "+%s" % iso_5p
variants = [
"iso_5p:%s" % iso_5p if v.startswith("iso_5p") else v
for v in variants
]
features.attributes["Variant"] = ",".join(variants)
features.attributes["UID"] = make_id(
read_uid_10(features.attributes["UID"]))
return features.paste_columns()
def variant_with_nt(line, precursors, matures):
"""
Return nucleotides changes for each variant type
using Variant attribute, precursor sequences and
mature position.
"""
gff = feature(line)
attr = gff.attributes
read = read_id(attr["UID"])
attr["Parent"] = attr["Parent"].split(",")[0]
if attr["Parent"] not in matures:
logger.warning("Parent miRNA not found in database %s" % attr["Parent"])
return ""
if attr["Name"] not in matures[attr["Parent"]]:
logger.warning("miRNA not found in database %s" % attr["Name"])
return ""
logger.debug("GFF::BODY::precursors %s" % precursors[attr["Parent"]])
logger.debug("GFF:BODY::mature %s" % matures[attr["Parent"]][attr["Name"]])
t5 = variant_to_5p(precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]],
attr["Variant"])
t3 = variant_to_3p(precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]],
attr["Variant"])
add = variant_to_add(read,
attr["Variant"])
mature_sequence = get_mature_sequence(
precursors[attr["Parent"]],
matures[attr["Parent"]][attr["Name"]],
nt=8)
logger.debug("GFF::BODY::mature_sequence %s" % mature_sequence)
mm = align_from_variants(read,
mature_sequence,
attr["Variant"])
if mm == "Invalid":
return mm
if len(mm) > 0:
mm = "".join(["".join([str(v) for v in m]) for m in mm])
else:
mm = "0"
return "iso_5p:%s,iso_3p:%s,iso_add3p:%s,iso_snv:%s" % (t5, t3, add, mm)
def _compare_to_reference(fn, reference):
same = 0
diff = list()
extra = list()
miss = list()
results = list()
seen = 0
seen_reference = set()
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
gff = feature(line)
attr = gff.attributes
if attr['UID'] in reference:
mirna = "Y" if attr['Name'] == reference[
attr['UID']][1]['Name'] else attr['Name']
accuracy = _accuracy(_simplify(attr['Variant']),
reference[attr['UID']][0])
results.append([attr['UID'], "D", mirna, accuracy])
if _simplify(attr['Variant']) == reference[attr['UID']][0]:
same += 1
else:
diff.append("%s | reference: %s" %
(line.strip(), reference[attr['UID']][1]))
seen += 1
seen_reference.add(attr['UID'])
else:
extra.append("%s | extra" % line.strip())
results.append([
attr['UID'], "E", attr['Name'],
_accuracy(_simplify(attr['Variant']), "")
])
for uid in reference:
if uid not in seen_reference:
results.append([uid, "M", "N", _accuracy("", reference[uid][0])])
miss.append("| miss %s" % reference[uid][1])
logger.info("Number of sequences found in reference: %s" % seen)
logger.info("Number of sequences matches reference: %s" % same)
logger.info("Number of sequences different than reference: %s" % len(diff))
logger.info("Number of sequences extra sequences: %s" % len(extra))
logger.info("Number of sequences missed sequences: %s" % len(miss))
return results
def _calc_stats(fn):
"""
Read files and parse into categories
"""
samples = _get_samples(fn)
lines = []
seen = set()
ok = re.compile('pass', re.IGNORECASE)
with open(fn) as inh:
for line in inh:
if line.startswith("#"):
continue
gff = feature(line)
cols = gff.columns
attr = gff.attributes
logger.debug("## STATS: attribute %s" % attr)
if not ok.match(attr['Filter']):
continue
if "-".join([attr['UID'], attr['Variant'], attr['Name']]) in seen:
continue
seen.add("-".join([attr['UID'], attr['Variant'], attr['Name']]))
lines.extend(_classify(cols['type'], attr, samples))
df = _summary(lines)
return df
def read_file(fn, args):
"""
Read isomiR-SEA file and convert to mirtop GFF format.
Args:
*fn(str)*: file name with isomiR-SEA output information.
*database(str)*: database name.
*args(namedtuple)*: arguments from command line.
See *mirtop.libs.parse.add_subparser_gff()*.
Returns:
*reads (nested dicts)*:gff_list has the format as
defined in *mirtop.gff.body.read()*.
"""
database = args.database
gtf = args.gtf
sep = " " if args.out_format == "gtf" else "="
map_mir = mapper.read_gtf_to_mirna(gtf)
reads = defaultdict(dict)
reads_in = 0
sample = os.path.splitext(os.path.basename(fn))[0]
hits = _get_hits(fn)
logger.debug("ISOMIRSEA::SAMPLE::%s" % sample)
with open(fn) as handle:
for line in handle:
cols = line.strip().split("\t")
attr = read_attributes(line, "=")
query_name = attr['TS']
query_sequence = attr['TS'].replace("U", "T")
start = int(cols[3])
end = int(cols[4])
isomirseq_iso = attr['ISO']
if query_name not in reads and query_sequence == None:
continue
if query_sequence and query_sequence.find("N") > -1:
continue
counts = attr["TC"]
chrom = cols[0]
# logger.debug("SEQBUSTER:: cigar {cigar}".format(**locals()))
cigar = attr['CI'].replace("U", "T")
idu = make_id(query_sequence)
isoformat = cigar2variants(cigar, query_sequence, attr['ISO'])
logger.debug("\nISOMIRSEA::NEW::query: {query_sequence}\n"
" precursor {chrom}\n"
" name: {query_name}\n"
" idu: {idu}\n"
" start: {start}\n"
" cigar: {cigar}\n"
" iso: {isoformat}\n"
" variant: {isoformat}".format(**locals()))
source = "isomiR" if isoformat != "NA" else "ref_miRNA"
strand = "+"
database = cols[1]
mirName = attr['MIN'].split()[0]
preName = attr['PIN'].split()[0]
score = "."
Filter = attr['FILTER']
isotag = attr['ISO']
tchrom, tstart = _genomic2transcript(map_mir[mirName], chrom,
start)
start = start if not tstart else tstart
chrom = chrom if not tstart else tchrom
end = start + len(query_sequence)
hit = hits[idu]
fields = {
'seq_name': query_sequence,
'idseq': idu,
'name': mirName,
'parent': preName,
'variant': isoformat,
'cigar': cigar,
'counts': counts,
'filter': Filter,
'hits': hit,
'chrom': chrom,
'start': start,
'end': end,
'database': database,
'source': source,
'score': score,
'strand': strand
}
# TODO: convert to genomic if args.out_genomic
line = feature(fields).line
if args.add_extra:
extra = variant_with_nt(line, args.precursors, args.matures)
line = "%s Changes %s;" % (line, extra)
line = paste_columns(feature(line), sep=sep)
if start not in reads[chrom]:
reads[chrom][start] = []
if Filter == "Pass":
reads_in += 1
reads[chrom][start].append([idu, chrom, counts, sample, line])
logger.info("Hits: %s" % reads_in)
return reads
def convert_gff_counts(args):
""" Reads a GFF file to produces output file containing Expression counts
Args:
*args(namedtuple)*: arguments parsed from command line with
*mirtop.libs.parse.add_subparser_counts()*.
Returns:
*file (file)*: with columns like:
UID miRNA Variant Sample1 Sample2 ... Sample N
"""
sep = "\t"
variant_header = sep.join(['iso_5p', 'iso_3p', 'iso_add3p', 'iso_snp'])
if args.add_extra:
precursors = fasta.read_precursor(args.hairpin, args.sps)
matures = mapper.read_gtf_to_precursor(args.gtf)
variant_header = sep.join([
variant_header, 'iso_5p_nt', 'iso_3p_nt', 'iso_add3p_nt',
'iso_snp_nt'
])
logger.info("INFO Reading GFF file %s", args.gff)
logger.info("INFO Writing TSV file to directory %s", args.out)
gff_file = open(args.gff, 'r')
out_file = op.join(args.out,
"%s.tsv" % op.splitext(op.basename(args.gff))[0])
missing_parent = 0
missing_mirna = 0
unvalid_uid = 0
with open(out_file, 'w') as outh:
for samples_line in gff_file:
if samples_line.startswith("## COLDATA:"):
samples = sep.join(samples_line.strip().split("COLDATA:")
[1].strip().split(","))
header = sep.join([
'UID', 'Read', 'miRNA', 'Variant', variant_header, samples
])
print(header, file=outh)
break
for mirna_line in gff_file:
gff = feature(mirna_line)
attr = gff.attributes
UID = attr["UID"]
Read = attr["Read"]
mirna = attr["Name"]
parent = attr["Parent"]
variant = attr["Variant"]
try:
read_id(UID)
except KeyError:
unvalid_uid += 1
continue
expression = sep.join(attr["Expression"].strip().split(","))
cols_variants = sep.join(_expand(variant))
logger.debug("COUNTS::Read:%s" % Read)
logger.debug("COUNTS::EXTRA:%s" % variant)
if args.add_extra:
if parent not in precursors:
missing_parent += 1
continue
if mirna not in matures[parent]:
missing_mirna += 1
continue
extra = variant_with_nt(mirna_line, precursors, matures)
if extra == "Invalid":
continue
logger.debug("COUNTS::EXTRA:%s" % extra)
cols_variants = sep.join([cols_variants] +
_expand(extra, True))
summary = sep.join(
[UID, Read, mirna, variant, cols_variants, expression])
logger.debug(summary)
print(summary, file=outh)
gff_file.close()
logger.info("Missing Parents in hairpin file: %s" % missing_parent)
logger.info("Missing MiRNAs in GFF file: %s" % missing_mirna)
logger.info("Non valid UID: %s" % unvalid_uid)
logger.info("Output file is at %s" % out_file)
def _fix(line, expression):
# Need to fix Read attribute since not usefull when multiple sample in a line.
gff = feature(line)
attr = gff.attributes
attr['Expression'] = expression
return paste_columns(gff, guess_format(line))
def create(reads, database, sample, args, quiet=False):
"""Read https://github.com/miRTop/mirtop/issues/9"""
sep = " " if args.out_format == "gtf" else "="
seen = set()
lines = defaultdict(defaultdict)
seen_ann = {}
filter_precursor = 0
filter_score = 0
n_hits = 0
n_reads = 0
n_seen = 0
if args.add_extra:
precursors = args.precursors
matures = args.matures
for (r, read) in reads.items():
hits = set()
[hits.add(mature.mirna) for mature in read.precursors.values()
if mature.mirna]
hits = len(hits)
if len(read.precursors) > 0:
n_reads += 1
for (ps, iso) in read.precursors.items():
p = list(ps)[0]
if not iso.mirna:
filter_precursor += 1
continue
if (r, iso.mirna) not in seen:
seen.add((r, iso.mirna))
chrom = p
seq = reads[r].sequence
seq_name = seq if not args.keep_name else r
if iso.get_score(len(seq)) < 1:
filter_score += 1
continue
if iso.subs:
iso.subs = [] if "N" in iso.subs[0] else iso.subs
idseq = reads[r].idseq
source = "ref_miRNA" if not iso.is_iso() else "isomiR"
strand = iso.strand
start, end = iso.start, iso.end
score = iso.map_score
mirName = iso.mirna
preName = p
Variant = iso.formatGFF()
Cigar = iso.cigar
counts = read.counts
Filter = iso.filter
annotation = "%s.%s.%s" % (chrom, idseq, seq_name)
# TODO: This need to be moved to use the feature class
# It needs a dict with all variable in keys
fields = {'seq_name': seq_name, 'idseq': idseq,
'name': mirName, 'parent': preName,
'variant': Variant, 'cigar': Cigar,
'counts': counts, 'filter': Filter,
'hits': hits, 'chrom': chrom,
'start': start, 'end': end,
'database': database, 'source': source,
'score': score, 'strand': strand}
line = feature(fields).line
logger.debug("GFF::%s" % line)
if args.add_extra:
extra = variant_with_nt(line, precursors, matures)
line = "%s Changes %s;" % (line, extra)
if annotation in seen_ann and seq.find("N") < 0 and (
seen_ann[annotation].split("\t")[0].find("N") < 0):
logger.warning(
"Same isomir %s from different sequence:"
" \n%s and \n%s" % (annotation, line,
seen_ann[annotation]))
seen_ann[annotation] = line
logger.debug("GFF::external %s" % iso.external)
if start not in lines[chrom]:
lines[chrom][start] = []
lines[chrom][start].append([annotation, chrom,
counts, sample, line])
logger.debug("GFF::%s" % line)
n_hits += 1
else:
n_seen += 1
if not quiet:
logger.info("GFF miRNAs: %s" % len(lines))
logger.info("GFF hits %s by %s reads" % (n_hits, n_reads))
logger.info("Filtered by being duplicated: %s" % n_seen)
logger.info("Filtered by being outside miRNA positions:"
" %s" % filter_precursor)
logger.info("Filtered by being low score: %s" % filter_score)
return lines
def read_file(folder, args):
"""
Read sRNAbench file and convert to mirtop GFF format.
Args:
*fn(str)*: file name with sRNAbench output information.
*database(str)*: database name.
*args(namedtuple)*: arguments from command line.
See *mirtop.libs.parse.add_subparser_gff()*.
Returns:
*reads (nested dicts)*:gff_list has the format as
defined in *mirtop.gff.body.read()*.
"""
reads_anno = os.path.join(folder, "reads.annotation")
reads_iso = os.path.join(folder, "microRNAannotation.txt")
sep = " " if args.out_format == "gtf" else "="
sample = os.path.basename(folder)
database = args.database
precursors = args.precursors
matures = args.matures
n_out = 0
n_in = 0
n_ns = 0
n_notassign = 0
n_notindb = 0
reads = defaultdict(dict)
seen = set()
source_iso = _read_iso(reads_iso)
logger.info("Reads with isomiR information %s" % len(source_iso))
with open(reads_anno) as handle:
for sequence in handle:
cols = sequence.strip().split("\t")
query_name = cols[0]
query_sequence = cols[0]
if query_name not in reads and not query_sequence:
continue
if query_sequence and query_sequence.find("N") > -1:
n_ns += 1
continue
if cols[3].find("mature") == -1:
n_in += 1
continue
counts = int(cols[1])
hits = len(
set([mirna.split("#")[1] for mirna in cols[4].split("$")]))
for nhit in cols[4].split("$"):
logger.debug("SRNABENCH::line hit: %s" % nhit)
hit_info = nhit.split("#")
pos_info = hit_info[3].split(",")
start = int(pos_info[1]) - 1
end = start + len(query_sequence) # int(pos_info[2]) - 1
chrom = pos_info[0]
mirName = hit_info[1]
if chrom not in precursors or chrom not in matures:
n_notindb += 1
if mirName not in matures[chrom]:
n_notindb += 1
if (query_sequence, mirName) in seen:
continue
seen.add((query_sequence, mirName))
if (query_sequence, mirName) not in source_iso:
continue
isoformat = source_iso[(query_sequence, mirName)]
if isoformat == "mv":
n_notassign += 1
continue
source = "isomiR" if isoformat != "NA" else "ref_miRNA"
logger.debug("SRNABENCH::query: {query_sequence}\n"
" precursor {chrom}\n"
" name: {query_name}\n"
" start: {start}\n"
" external: {isoformat}\n"
" hit: {hits}".format(**locals()))
logger.debug("SRNABENCH:: start %s end %s" % (start, end))
if len(precursors[chrom]) < start + len(query_sequence):
n_out += 1
continue
Filter = "Pass"
cigar = make_cigar(query_sequence,
precursors[chrom][start:end])
preName = chrom
score = "."
strand = "+"
idu = make_id(query_sequence)
# attrb = ("Read {query_sequence}; UID {idu}; Name {mirName};"
# " Parent {preName}; Variant {isoformat};"
# " Cigar {cigar}; Expression {counts};"
# " Filter {Filter}; Hits {hits};").format(**locals())
# line = ("{chrom}\t{database}\t{source}\t{start}\t{end}\t"
# "{score}\t{strand}\t.\t{attrb}").format(**locals())
fields = {
'seq_name': query_sequence,
'idseq': idu,
'name': mirName,
'parent': preName,
'variant': isoformat,
'cigar': cigar,
'counts': counts,
'filter': Filter,
'hits': hits,
'chrom': chrom,
'start': start,
'end': end,
'database': database,
'source': source,
'score': score,
'strand': strand
}
# TODO: convert to genomic if args.out_genomic
line = feature(fields).line
if args.add_extra:
extra = variant_with_nt(line, args.precursors,
args.matures)
line = "%s Changes %s;" % (line, extra)
line = paste_columns(feature(line), sep=sep)
if start not in reads[chrom]:
reads[chrom][start] = []
if Filter == "Pass":
n_in += 1
reads[chrom][start].append(
[idu, chrom, counts, sample, line])
logger.info("Loaded %s reads with %s hits" % (len(reads), n_in))
logger.info("Reads without precursor information: %s" % n_notindb)
logger.info("Reads with MV as variant definition,"
" not supported by GFF: %s" % n_notassign)
logger.info("Hit Filtered by having > 3 changes: %s" % n_out)
return reads
def _analyze_line(line, precursors, database, sample, sep, args):
start_idx = 10
end_idx = 11
attr_idx = 15
query_name = line[3]
sequence = line[4]
if str(line).find(get_primary_transcript(guess_database(args))) < 0: # only working with mirbase
return None
logger.debug(("READ::line name:{0}").format(line))
if sequence and sequence.find("N") > -1:
return None
chrom = line[attr_idx].strip().split("Name=")[-1]
start = line[1]
end = line[2]
strand = line[5]
counts = float(line[6])
Filter = "Pass"
reads = dict()
if not start:
return None
if strand == "+":
start = int(start) - int(line[start_idx]) + 1
else:
start = int(line[end_idx]) - int(end)
iso = isomir()
iso.align = line
iso.set_pos(start, len(sequence))
logger.debug("READ::From BAM start %s end %s at chrom %s" % (iso.start, iso.end, chrom))
if len(precursors[chrom]) < start + len(sequence):
logger.debug("READ::%s start + %s sequence size are bigger than"
" size precursor %s" % (
chrom,
len(sequence),
len(precursors[chrom])))
iso.subs, iso.add, iso.cigar = filter.tune(
sequence, precursors[chrom],
start, None)
logger.debug("READ::After tune start %s end %s" % (iso.start, iso.end))
logger.debug("READ::iso add %s iso subs %s" % (iso.add, iso.subs))
idu = make_id(sequence)
reads[query_name] = hits()
reads[query_name].set_sequence(sequence)
reads[query_name].counts = counts
reads[query_name].sequence = sequence
reads[query_name].set_precursor(chrom, iso)
reads = annotate(reads, args.matures, args.precursors, quiet=True)
gff_line = body.create(reads, args.database, sample, args, quiet=True)
if start not in gff_line[chrom]:
return None
line = gff_line[chrom][start][0][4]
logger.debug("READ::line:%s" % line)
if args.add_extra:
extra = variant_with_nt(line, args.precursors,
args.matures)
line = "%s Changes %s;" % (line, extra)
line = paste_columns(feature(line), sep=sep)
return {'chrom': chrom,
'start': start,
'name': query_name,
'mirna': reads[query_name].precursors[chrom].mirna,
'line': [idu, chrom, counts, sample, line]}
