def parse_sequences(sites, size, fasta_file):
"""Adds the binding site sequences extende to 'size' per row (decoded as A=0, C=1, G=2, T=3) to each input region."""
from pyfasta import Fasta # Fasta package is needed to fetch sequences from genome fasta file
print "INFO: Begin to fetch sequences...."
f = Fasta(fasta_file, key_fn=lambda key: key.split()[0])
for i, reg in enumerate(sites):
start = reg["ext_start"]
end = reg["ext_end"]
# if motif on negativ strand, shift region by +1 to account for zero based half-open intervals
if reg["strand"] == '-':
start += 1
end += 1
seq = f.sequence({"chr":reg["chr"], "start":start, "stop":end}, one_based=False)
# Note, the 'strand':reg["strand"] argument for f.sequence does not work, there seems to be a bug in the pyfasta/fasta.py code.
seq = seq.upper()
# if motif on negative strand, convert seq to reverse complement
if reg["strand"] == '-':
seq = reverse_complement(seq)
# add sequence to region dict
reg["ext_seq"] = seq
print "INFO: Finished sequences."
return regions
def getSequence(genome):
genome=Fasta(genome)
RAD_seq = pd.read_csv('../data/input_data/peak.csv')
result = map(lambda i:[genome.sequence({'chr':RAD_seq['chrom'][i],'start':RAD_seq['start'][i],'stop':RAD_seq['end'][i]})],range(len(RAD_seq)))
RAD_seq['seq'] = result
RAD_seq['seq'] = RAD_seq.apply(fuc,axis=1)
RAD_seq.to_csv('../data/input_data/RAD_seq.csv',index=False)
print 'getSequence is over,RAD_seq.csv is bulit!'
class Reference(object):
def __init__(self, genome_fasta):
# @see: https://pypi.python.org/pypi/pyfasta
key_fn = lambda key : key.split()[0] # Use first value before whitespace as keys
self.fasta = Fasta(genome_fasta, key_fn=key_fn)
def get_sequence_from_iv(self, iv):
feature_hash = {'chr' : iv.chrom, 'start' : iv.start, 'stop' : iv.end, 'strand' : iv.strand}
return self.fasta.sequence(feature_hash, one_based=False)
class GenomeSeq(object):
""" genomic sequence"""
def __init__(self,filename):
self.filename = filename
self.fh = Fasta(filename, key_fn = get_chrom)
def get_seq(self,chrom,start=0,end=False,strand="+"):
if end is False:
end = len(self.fh[chrom])
return self.fh.sequence({"chr":chrom, "start":start, "stop": end, "strand":strand}, one_based=False)
def extract_only_ref_variant_fasta():
f = Fasta(args.reference)
if len(f.keys()) == 1:
ref_id = str(f.keys())
ffp = open("%s/Only_ref_variant_positions_for_closely" %
args.filter2_only_snp_vcf_dir).readlines()
core_vcf_file = args.filter2_only_snp_vcf_filename.replace(
'_filter2_final.vcf_no_proximate_snp.vcf',
'_filter2_final.vcf_core.vcf.gz')
fasta_string = ""
count = 0
for lines in ffp:
lines = lines.strip()
grep_position = "zcat %s | grep -v \'#\' | awk -F\'\\t\' \'{ if ($2 == %s) print $0 }\' | awk -F\'\\t\' \'{print $5}\'" % (
core_vcf_file, lines)
proc = subprocess.Popen([grep_position],
stdout=subprocess.PIPE,
shell=True)
(out, err) = proc.communicate()
out = out.strip()
if out:
if "," in out:
split = out.split(',')
fasta_string = fasta_string + split[0]
print "HET SNP found: Position:%s; Taking the First SNP:%s" % (
lines, split[0])
count += 1
else:
fasta_string = fasta_string + out
count += 1
else:
fasta_string = fasta_string + str(
f.sequence({
'chr': str(f.keys()[0]),
'start': int(lines),
'stop': int(lines)
}))
count += 1
pattern = re.compile(r'\s+')
fasta_string = re.sub(pattern, '', fasta_string)
final_fasta_string = ">%s\n" % os.path.basename(
core_vcf_file.replace('_filter2_final.vcf_core.vcf.gz',
'')) + fasta_string
fp = open(
"%s/%s_variants.fa" %
(args.filter2_only_snp_vcf_dir,
os.path.basename(
core_vcf_file.replace('_filter2_final.vcf_core.vcf.gz', ''))),
'w+')
fp.write(final_fasta_string + '\n')
fp.close()
def main(gff_file, outdir):
"""empty docstring"""
name = re.compile("parent=([^.;]+)", re.I)
feats = {}
non_cds_feats = collections.defaultdict(list)
for line in open(gff_file):
line = line.split("\t")
match = re.search(name, line[-1])
if not match:
continue
fname = match.groups(0)[0]
non_cds_feats[fname].append(line)
if line[2].upper() == "CDS":
feats[fname] = True
continue
if fname in feats:
continue
feats[fname] = None
i = 0
for k, v in sorted(feats.items()):
if not v is None:
del non_cds_feats[k]
seen = {}
RNA = open(outdir + "/at_non_cds.gff", "w")
for k, feat_list in sorted(non_cds_feats.items()):
for feat in feat_list:
if feat[0] in ("ChrC", "ChrM"):
continue
if feat[2] == "exon":
continue
key = (feat[0], feat[3], feat[4])
if key in seen:
continue
feat[0] = feat[0].upper().replace("CHR", "")
seen[key] = True
feat[-1] = k
print >> RNA, "\t".join(feat)
RNA.close()
gff = read_gff(outdir + "/at_non_cds.gff")
fasta = Fasta("/home/gturco/src/find_cns_gturco/pipeline/data/arabidopsis.fasta")
ftypes = {}
FA = open(outdir + "/at_rnas.fasta", "w")
for chr, feature_list in gff.iteritems():
for fname, feature in feature_list.iteritems():
seq = fasta.sequence(feature)
print >> FA, ">", feature["name"]
print >> FA, seq
FA.close()
def main(gff_file, outdir):
"""empty docstring"""
name = re.compile("parent=([^.;]+)", re.I)
feats = {}
non_cds_feats = collections.defaultdict(list)
for line in open(gff_file):
line = line.split("\t")
match = re.search(name, line[-1])
if not match: continue
fname = match.groups(0)[0]
non_cds_feats[fname].append(line)
if line[2].upper() == 'CDS':
feats[fname] = True
continue
if fname in feats: continue
feats[fname] = None
i = 0
for k, v in sorted(feats.items()):
if not v is None: del non_cds_feats[k]
seen = {}
RNA = open(outdir + '/at_non_cds.gff', 'w')
for k, feat_list in sorted(non_cds_feats.items()):
for feat in feat_list:
if feat[0] in ('ChrC', 'ChrM'): continue
if feat[2] == 'exon': continue
key = (feat[0], feat[3], feat[4])
if key in seen: continue
feat[0] = feat[0].upper().replace('CHR', '')
seen[key] = True
feat[-1] = k
print >> RNA, "\t".join(feat)
RNA.close()
gff = read_gff(outdir + '/at_non_cds.gff')
fasta = Fasta(
'/home/gturco/src/find_cns_gturco/pipeline/data/arabidopsis.fasta')
ftypes = {}
FA = open(outdir + '/at_rnas.fasta', 'w')
for chr, feature_list in gff.iteritems():
for fname, feature in feature_list.iteritems():
seq = fasta.sequence(feature)
print >> FA, ">", feature['name']
print >> FA, seq
FA.close()
def run(args):
genome = Fasta(args.genome)
bed = filter(lambda x: x.strip(), args.bedfile.readlines())
bed_list = map(lambda x: x.strip().split(), bed)
result = map(
lambda i: '>{0}_{1}\n{2}'.format(
args.seqname, i + 1,
genome.sequence({
'chr': bed_list[i][0],
'start': int(bed_list[i][1]) - args.flank,
'stop': int(bed_list[i][2]) + args.flank,
'strand': bed_list[i][3]
})).upper(), range(len(bed_list)))
if args.outfile:
args.outfile.write('\n'.join(result))
else:
print ''.join(result)
def intron(fa, ann):
f = Fasta(fa)
fh = open(ann, 'r')
out1 = open('intron.fa', 'w')
mdict = {}
ndict = {}
for line in fh:
if line.startswith('#'):
continue
new = line.strip().split('\t')
if new[2] != 'CDS':
continue
n = new[-1].split(';')
for i, j in enumerate(n):
if 'Parent=' in j:
mindex = i
g = n[mindex].split('.')
t = g[0].replace('Parent=', '')
if '_' in t:
gene = t.split('_')[0]
else:
gene = t
if gene not in mdict:
mdict[gene] = []
ndict[gene] = [new[0], new[6]]
start1 = int(new[3])
stop1 = int(new[4])
mdict[gene].append((start1, stop1))
for i in sorted(mdict):
k = ''
total = len(mdict[i])
for j in range(0, total - 1):
start = mdict[i][j][1] + 1
stop = mdict[i][j + 1][0] - 1
k1 = f.sequence({
'chr': ndict[i][0],
'start': start,
'stop': stop,
'strand': ndict[i][1]
})
k += k1
out1.write('>{0}-intron'.format(i) + '\n')
out1.write(k + '\n')
fh.close()
out1.close()
def extract_reference_allele():
print "Extracting Reference Allele from Reference Fasta file - %s to REF\n" % args.reference
# Get reference genome ID from reference fasta file
get_reference = Fasta(args.reference)
if len(get_reference.keys()) == 1:
ref_id = get_reference.keys()
print "The reference genome ID from reference genome - %s" % ref_id
fileObj = open("REF", 'w+')
fileObj.write('Ref' + '\n')
for item in pos:
ref_allele = str(
get_reference.sequence({
'chr': str(get_reference.keys()[0]),
'start': int(item),
'stop': int(item)
}))
fileObj.write(ref_allele + '\n')
fileObj.close()
def parse_sequences(sites, size, fasta_file):
"""Adds the binding site sequences extende to 'size' per row (decoded as A=0, C=1, G=2, T=3) to each input region."""
from pyfasta import Fasta # Fasta package is needed to fetch sequences from genome fasta file
print "INFO: Begin to fetch sequences...."
f = Fasta(fasta_file, key_fn=lambda key: key.split()[0])
for i, reg in enumerate(sites):
start = reg["ext_start"]
end = reg["ext_end"]
# if motif on negativ strand, shift region by +1 to account for zero based half-open intervals
if reg["strand"] == '-':
start += 1
end += 1
seq = f.sequence({
"chr": reg["chr"],
"start": start,
"stop": end
},
one_based=False)
# Note, the 'strand':reg["strand"] argument for f.sequence does not work, there seems to be a bug in the pyfasta/fasta.py code.
seq = seq.upper()
# if motif on negative strand, convert seq to reverse complement
if reg["strand"] == '-':
seq = reverse_complement(seq)
# add sequence to region dict
reg["ext_seq"] = seq
print "INFO: Finished sequences."
return regions
def main(gff_file, fasta_file, parents, children):
db_file = gff_file + ".db"
if not op.exists(db_file):
GFFutils.create_gffdb(gff_file, db_file)
f = Fasta(fasta_file)
g = GFFutils.GFFDB(db_file)
parents = set(parents.split(','))
parents_iter = [g.features_of_type(x) for x in parents]
parents_list = itertools.chain(*parents_iter)
children_list = set(children.split(','))
for feat in parents_list:
children = []
for c in g.children(feat.id, 1):
if c.featuretype not in children_list: continue
child = f.sequence(
dict(chr=c.chrom, start=c.start, stop=c.stop, strand=c.strand))
children.append((child, c))
if not children:
print >>sys.stderr, "[warning] %s has no children with type %s" \
% (feat.id, ','.join(children_list))
continue
# sort children in incremental position
children.sort(key=lambda x: x[1].start)
# reverse children if negative strand
if feat.strand == '-': children.reverse()
feat_seq = ''.join(x[0] for x in children)
print ">%s" % feat.id
print feat_seq
def main(gff_file, fasta_file, parents, children):
db_file = gff_file + ".db"
if not op.exists(db_file):
GFFutils.create_gffdb(gff_file, db_file)
f = Fasta(fasta_file)
g = GFFutils.GFFDB(db_file)
parents = set(parents.split(','))
parents_iter = [g.features_of_type(x) for x in parents]
parents_list = itertools.chain(*parents_iter)
children_list = set(children.split(','))
for feat in parents_list:
children = []
for c in g.children(feat.id, 1):
if c.featuretype not in children_list: continue
child = f.sequence(dict(chr=c.chrom, start=c.start, stop=c.stop,
strand=c.strand))
children.append((child, c))
if not children:
print >>sys.stderr, "[warning] %s has no children with type %s" \
% (feat.id, ','.join(children_list))
continue
# sort children in incremental position
children.sort(key=lambda x: x[1].start)
# reverse children if negative strand
if feat.strand=='-': children.reverse()
feat_seq = ''.join(x[0] for x in children)
print ">%s" % feat.id
print feat_seq
#version 1.1 此版本使用pyfasta实现。
import sys, os
from pyfasta import Fasta
if len(sys.argv) != 3:
print 'Usage: *.py inputFile outputFile'
sys.exit(0)
inputFile = sys.argv[1]
outputFile = sys.argv[2]
def writeFile(text, files):
with open(files, 'a') as f:
f.write(text)
if os.path.isfile(inputFile):
f = Fasta(inputFile)
for key in f.keys():
writeFile(">" + key + os.linesep, outputFile)
content = f.sequence(
{
'chr': key,
'start': 0,
'stop': len(f[key]) - 1,
'strand': '-'
},
one_based=False)
writeFile(content + os.linesep, outputFile)
else:
print '您输入的不是一个文件'
def downstream(fa, ann, kb1, kb2):
'''
Extracting gene upstream sequences. fa is genome assembly file, ann is
the annotation file, kb1 is the defined length of 3' UTR, kb2 is the defined
length of downstream.
'''
f = Fasta(fa)
fh = open(ann, 'r')
out1 = open('3-UTR.fa', 'w')
out2 = open('downstream.fa', 'w')
mdict = {}
ndict = {}
for line in fh:
# this is the demo line that we want to filter out
# chr7 GLEAN Gene 25420153 25421713 0.953889 - . Name=Pgl_GLEAN_10006696;
if line.startswith('#'):
continue
new = line.strip().split('\t')
if new[2] != 'CDS':
continue
n = new[-1].split(';')
for i, j in enumerate(n):
if 'Parent=' in j:
mindex = i
g = n[mindex].split('.')
t = g[0].replace('Parent=', '')
if '_' in t:
gene = t.split('_')[0]
else:
gene = t
if gene not in mdict:
mdict[gene] = []
ndict[gene] = []
ndict[gene].append(new[0])
ndict[gene].append(new[6])
mdict[gene].append(int(new[3]))
mdict[gene].append(int(new[4]))
for gene in sorted(mdict):
if ndict[gene][1] == '+':
stop = max(mdict[gene])
start1 = stop + 1
stop1 = stop + (int(kb1) + 1)
start2 = stop1 + 1
stop2 = stop1 + (int(kb2) + 1)
k1 = f.sequence({
'chr': ndict[gene][0],
'start': start1,
'stop': stop1,
'strand': ndict[gene][1]
})
out1.write('>{0}-3UTR'.format(gene) + '\n')
out1.write(k1 + '\n')
k2 = f.sequence({
'chr': ndict[gene][0],
'start': start2,
'stop': stop2,
'strand': ndict[gene][1]
})
out2.write('>{0}-downstream'.format(gene) + '\n')
out2.write(k2 + '\n')
elif ndict[gene][1] == '-':
start = min(mdict[gene])
start1 = start - (int(kb1) + 1)
stop1 = start - 1
start2 = start1 - (int(kb2) + 1)
stop2 = start1 - 1
k1 = f.sequence({
'chr': ndict[gene][0],
'start': start1,
'stop': stop1,
'strand': ndict[gene][1]
})
out1.write('>{0}-3UTR'.format(gene) + '\n')
out1.write(k1 + '\n')
k2 = f.sequence({
'chr': ndict[gene][0],
'start': start2,
'stop': stop2,
'strand': ndict[gene][1]
})
out2.write('>{0}-downstream'.format(gene) + '\n')
out2.write(k2 + '\n')
fh.close()
out1.close()
out2.close()
if not out:
f = Fasta(reference)
if len(f.keys()) == 1:
ref_id = str(f.keys())
fasta_string = ""
extract_base = "tr -d \'\\n\' < %s | cut -b%s" % (reference, j)
#print extract_base
# proc = subprocess.Popen([extract_base], stdout=subprocess.PIPE, shell=True)
# (out, err) = proc.communicate()
# out = out.strip()
# fasta_string = fasta_string + out
# if not out:
# print "Error extracting reference allele"
#out = str(f.sequence({'chr': str(f.keys()[0]), 'start': int(lines), 'stop': int(lines)}))
fasta_string = fasta_string + str(f.sequence({'chr': str(f.keys()[0]), 'start': int(j), 'stop': int(j)}))
pattern = re.compile(r'\s+')
fasta_string = re.sub(pattern, '', fasta_string)
st = fasta_string + fasta_string + "\n"
f1.write(st)
else:
cmd2 = "grep -P \'\s+" + j + "\s+\' " + args.filter2_only_snp_vcf_file
#cmd2 = "grep -v \'^#\' %s | awk -F\'\t\' \'{print $2}\' | grep -w \'%s\'" % (final_file, j)
proc = subprocess.Popen([cmd2], stdout=subprocess.PIPE, shell=True)
(out2, err2) = proc.communicate()
line_string_array = out2.split('\t')
print line_string_array
ref_allele = line_string_array[3]
alt_allel = line_string_array[4]
def extract_only_ref_variant_fasta_alternate():
# Get reference genome ID
f = Fasta(args.reference)
if len(f.keys()) == 1:
ref_id = str(f.keys())
if args.functional_filter == "yes":
functional_filter_pos_array = []
functional_class_filter_positions = args.filter2_only_snp_vcf_dir + "/Functional_class_filter_positions.txt"
with open(functional_class_filter_positions, 'rU') as f_functional:
for line_func in f_functional:
functional_filter_pos_array.append(line_func.strip())
only_ref_variant = []
ffp = open(
"%s/Only_ref_variant_positions_for_closely" %
args.filter2_only_snp_vcf_dir, 'r+')
for line in ffp:
line = line.strip()
if line not in functional_filter_pos_array:
only_ref_variant.append(line)
ffp.close()
else:
only_ref_variant = []
ffp = open(
"%s/Only_ref_variant_positions_for_closely" %
args.filter2_only_snp_vcf_dir, 'r+')
for line in ffp:
line = line.strip()
only_ref_variant.append(line)
ffp.close()
print len(only_ref_variant)
# # Get Only_ref_variant positions list
# only_ref_variant = []
# ffp = open("%s/Only_ref_variant_positions_for_closely" % args.filter2_only_snp_vcf_dir, "r")
# for lines in ffp:
# lines = lines.strip()
# only_ref_variant.append(lines)
# ffp.close()
core_vcf_file = args.filter2_only_snp_vcf_filename.replace(
'_filter2_final.vcf_no_proximate_snp.vcf',
'_filter2_final.vcf_core.vcf.gz')
# print core_vcf_file
core_vcf_pos_base = {}
for variants in VCF("%s" % core_vcf_file):
if len(variants.ALT) > 1:
core_vcf_pos_base[variants.POS] = variants.ALT[0]
else:
core_vcf_pos_base[variants.POS] = variants.ALT
ffp.close()
#troubleshoot
# print len(core_vcf_pos_base)
# test = "2024"
# print str(core_vcf_pos_base[int(test)][0])
fasta_string = ""
count = 0
for lines in only_ref_variant:
lines = lines.strip()
if int(lines) in core_vcf_pos_base.keys():
# print lines
fasta_string = fasta_string + str(core_vcf_pos_base[int(lines)][0])
count += 1
else:
fasta_string = fasta_string + str(
f.sequence({
'chr': str(f.keys()[0]),
'start': int(lines),
'stop': int(lines)
}))
count += 1
pattern = re.compile(r'\s+')
fasta_string = re.sub(pattern, '', fasta_string)
final_fasta_string = ">%s\n" % os.path.basename(
core_vcf_file.replace('_filter2_final.vcf_core.vcf.gz',
'')) + fasta_string
fp = open(
"%s/%s_variants.fa" %
(args.filter2_only_snp_vcf_dir,
os.path.basename(
core_vcf_file.replace('_filter2_final.vcf_core.vcf.gz', ''))),
'w+')
fp.write(final_fasta_string + '\n')
fp.close()
# print final_fasta_string
print "Count: %s " % count
print "Length: %s " % len(fasta_string)
class MutateFasta(object):
def __init__(self, fasta):
self.fasta = Fasta(fasta, key_fn=lambda key: key.split()[0])
# self.chroms = [str(i+1) for i in range(22)] + ['X', 'Y'] # , 'MT']
def generate_seq(self, records, offset=None):
if not records and not offset: return
seq = ''
chrom = offset[0] if offset else records[0]['chrom']
prev_pos = offset[1] if offset else 0
last_pos = offset[2] if offset else len(self.fasta[chrom])
for r in records:
ref = self.slice_fasta(r['chrom'], r['pos'], r['pos'])
if not r['chrom'] == chrom: continue
if not (r['ref'] and r['alt']): continue
if not r['ref'][0] == ref: continue
mut_type, sub_seq = self._classify_mut(r['ref'], r['alt'])
if mut_type == 'snv':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'] - 1)
seq += sub_seq
prev_pos = r['pos']
elif mut_type == 'del':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'])
prev_pos += len(sub_seq)
elif mut_type == 'ins':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'])
seq += sub_seq
prev_pos = r['pos']
# Reminder
if prev_pos + 1 <= last_pos:
seq += self.slice_fasta(chrom, prev_pos + 1, last_pos)
return seq
def generate_contexted_seq(self, r):
cons = []
chrom = r['chrom']
# TODO: support - strand genes. (currently only supports + strand genes...)
# NOTE: refFlat is stored in 0-based coordinate
# 5'UTR + 1st Exon
cons.append(
[self.slice_fasta(chrom, r['txStart'] + 1, r['cdsStart']), 'utr'])
cons.append([
self.slice_fasta(chrom, r['cdsStart'] + 1, r['exonEnds'][0]),
'exon'
])
if r['exonCount'] > 1:
cons.append([
self.slice_fasta(chrom, r['exonEnds'][0] + 1,
r['exonStarts'][1]), 'intron'
])
# Exons
for i, con in enumerate(r['exonStarts']):
if i == 0 or i + 1 == r['exonCount']: continue
cons.append([
self.slice_fasta(chrom, r['exonStarts'][i] + 1,
r['exonEnds'][i]), 'exon'
])
cons.append([
self.slice_fasta(chrom, r['exonEnds'][i] + 1,
r['exonStarts'][i + 1]), 'intron'
])
# last Exon + 3'UTR
cons.append([
self.slice_fasta(chrom,
r['exonStarts'][r['exonCount'] - 1] + 1,
r['cdsEnd']), 'exon'
])
cons.append(
[self.slice_fasta(chrom, r['cdsEnd'] + 1, r['txEnd']), 'utr'])
return cons
def slice_fasta(self, chrom, start, stop):
return self.fasta.sequence(
{
'chr': str(chrom),
'start': int(start),
'stop': int(stop)
},
one_based=True)
def _classify_mut(self, ref, alt):
"""
>>> _classify_mut('A','G')
('snv', 'G')
>>> _classify_mut('G','GAA')
('ins', 'AA')
>>> _classify_mut('TTA','T')
('del', 'TA')
"""
if len(ref) == len(alt) == 1:
return 'snv', alt
elif len(ref) < len(alt):
assert ref[0] == alt[0], '{0} {1}'.format(ref, alt)
return 'ins', alt[1:]
elif len(ref) > len(alt):
assert ref[0] == alt[0], '{0} {1}'.format(ref, alt)
return 'del', ref[1:]
def extract_only_ref_variant_fasta_unique_positions():
#print "here"
# Get reference genome ID
get_reference = Fasta(args.reference)
if len(get_reference.keys()) == 1:
ref_id = get_reference.keys()
c_reader = csv.reader(open('%s/SNP_matrix_allele_new.csv' % args.filter2_only_snp_vcf_dir, 'r'), delimiter='\t')
c_reader_2 = csv.reader(open('%s/SNP_matrix_allele_new.csv' % args.filter2_only_snp_vcf_dir, 'r'), delimiter='\t')
columns = list(zip(*c_reader))
ncol = len(next(c_reader_2))
unique_position_array = []
for i in columns[0][1:]:
replace_string = i.split(' ')
if replace_string[0] != "None":
unique_position_array.append(int(replace_string[3]))
else:
unique_position_array.append(int(replace_string[2]))
#print unique_position_array
counts = 1
end = ncol
for i in xrange(1, end, 1):
print_string = ""
ref_print_string = ""
grab_vcf_filename = len(os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''))
#print grab_vcf_filename
sample_name_re = columns[i][0][:grab_vcf_filename]
#print sample_name_re
# Replaced this with a more stable check
#sample_name = str(columns[i][0])
# sample_name_re = re.sub('_R1.fastq.gz', '', sample_name)
# sample_name_re = re.sub('_R1_001.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_L001.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_*1*.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_S.*', '', sample_name_re)
if sample_name_re == os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', '') or sample_name_re in os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''):
vcf_header = "##fileformat=VCFv4.2\n#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\t%s\n" % sample_name_re
print_string = print_string + ">%s\n" % sample_name_re
ref_print_string = ref_print_string + ">%s\n" % sample_name_re
#variant_allele = ''.join(columns[i][1:])
variant_allele = ""
for ntd in columns[i][1:]:
if "/" in ntd:
variant_allele = variant_allele + ntd[0]
else:
variant_allele = variant_allele + ntd
#print variant_allele
print_string = print_string + str(variant_allele) + "\n"
allele_variant_fasta = open("%s/%s_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_variant_fasta.write(print_string)
allele_variant_fasta.close()
allele_ref_variant_fasta = open("%s/%s_ref_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_ref_variant_vcf = open("%s/%s_ref_allele_variants.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_ref_variant_vcf.write(vcf_header)
variant_allele_array = []
variant_allele_array.append(columns[i][1:])
get_sample_reference = Fasta("%s/%s_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re))
if len(get_sample_reference.keys()) == 1:
sample_ref_id = get_sample_reference.keys()
for positions in unique_position_array:
pos_index = unique_position_array.index(positions)
if "/" in str(variant_allele_array[0][pos_index]):
allele_var = str(variant_allele_array[0][pos_index][0])
#print allele_var
else:
allele_var = str(variant_allele_array[0][pos_index])
ref_allele = str(get_reference.sequence({'chr': str(get_reference.keys()[0]), 'start': int(positions), 'stop': int(positions)}))
generate_vcf_string = "%s\t%s\t.\t%s\t%s\t221.999\t.\t.\t.\n" % (ref_id[0].split(' ')[0], positions, ref_allele, allele_var)
allele_ref_variant_vcf.write(generate_vcf_string)
allele_ref_variant_vcf.close()
filename = "%s/consensus_ref_allele_variant.sh" % args.filter2_only_snp_vcf_dir
vcf_filename = "%s/%s_ref_allele_variants.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re)
f1 = open(filename, 'a+')
bgzip_cmd = "%s/%s/bgzip -f %s\n" % (ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'], vcf_filename)
f1.write(bgzip_cmd)
subprocess.call([bgzip_cmd], shell=True)
tabix_cmd = "%s/%s/tabix -f -p vcf %s.gz\n" % (ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'], vcf_filename)
f1.write(tabix_cmd)
subprocess.call([tabix_cmd], shell=True)
base_vcftools_bin = ConfigSectionMap("bin_path", Config)['binbase'] + "/" + ConfigSectionMap("vcftools", Config)['vcftools_bin']
fasta_cmd = "cat %s | %s/vcf-consensus %s.gz > %s_ref_allele_variants.fa\n" % (args.reference, base_vcftools_bin, vcf_filename, sample_name_re)
f1.write(fasta_cmd)
subprocess.call([fasta_cmd], shell=True)
sed_command = "sed -i 's/>.*/>%s/g' %s_ref_allele_variants.fa\n" % (sample_name_re, sample_name_re)
subprocess.call([sed_command], shell=True)
f1.write(sed_command)
#os.system("bash %s" % filename)
#sequence_lgth_cmd = "for i in %s/*.fa; do %s/%s/bioawk -c fastx \'{ print $name, length($seq) }\' < $i; done" % (args.filter2_only_snp_vcf_dir, ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("bioawk", Config)['bioawk_bin'])
#os.system(sequence_lgth_cmd)
#call("%s" % sequence_lgth_cmd, logger)
else:
print "Sample name %s does not match with column name %s" % (os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''), sample_name_re)
def extract_only_ref_variant_fasta_unique_positions_with_unmapped():
# Get reference genome ID from reference fasta file
get_reference = Fasta(args.reference)
if len(get_reference.keys()) == 1:
ref_id = get_reference.keys()
# Read in the SNP Matrix file and seperate the columns.
c_reader = csv.reader(open('%s/SNP_matrix_allele_new.csv' % args.filter2_only_snp_vcf_dir, 'r'), delimiter='\t')
c_reader_2 = csv.reader(open('%s/SNP_matrix_allele_new.csv' % args.filter2_only_snp_vcf_dir, 'r'), delimiter='\t')
columns = list(zip(*c_reader))
ncol = len(next(c_reader_2))
# Generate an array of all the unique variant positions that were called in all the samples
unique_position_array = []
for i in columns[0][1:]:
replace_string = i.split(' ')
if replace_string[0] != "None":
unique_position_array.append(int(replace_string[3]))
else:
unique_position_array.append(int(replace_string[2]))
counts = 1
end = ncol
# Loop over each column, check if the column name matches the sample name provided with argument args.filter2_only_snp_vcf_filename
for i in xrange(1, end, 1):
print_string = ""
ref_print_string = ""
grab_vcf_filename = len(os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''))
#print grab_vcf_filename
sample_name_re = columns[i][0][:grab_vcf_filename]
#print sample_name_re
# Replaced this with a more stable check
#sample_name = str(columns[i][0])
# sample_name_re = re.sub('_R1.fastq.gz', '', sample_name)
# sample_name_re = re.sub('_R1_001.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_L001.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_*1*.fastq.gz', '', sample_name_re)
# sample_name_re = re.sub('_S.*', '', sample_name_re)
#print len(columns[i][1:])
if sample_name_re == os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', '') or sample_name_re in os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''):
vcf_header = "##fileformat=VCFv4.2\n#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\t%s\n" % sample_name_re
print_string = print_string + ">%s\n" % sample_name_re
ref_print_string = ref_print_string + ">%s\n" % sample_name_re
#variant_allele = ''.join(columns[i][1:])
variant_allele = ""
for ntd in columns[i][1:]:
#if "/" in ntd:
if "/" in ntd or len(ntd) > 1:
variant_allele = variant_allele + ntd[0]
else:
variant_allele = variant_allele + ntd
#print variant_allele
print_string = print_string + str(variant_allele) + "\n"
allele_variant_fasta = open("%s/%s_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_ref_variant_fasta = open("%s/%s_ref_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_ref_variant_vcf = open("%s/%s_ref_allele_variants.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
allele_ref_variant_vcf.write(vcf_header)
allele_variant_fasta.write(print_string)
allele_variant_fasta.close()
variant_allele_array = []
variant_allele_array_dict = {}
#variant_allele_array.append(columns[i][1:])
count_index = 0
end_index = len(unique_position_array) + 1
for start_count in xrange(1, end_index, 1):
pos = columns[0][start_count]
get_positions_string = pos.split(' ')
if get_positions_string[0] != "None":
get_positions = int(get_positions_string[3])
else:
get_positions = int(get_positions_string[2])
variant_allele_array_dict[get_positions] = columns[i][start_count]
# print len(variant_allele_array_dict)
# print len(unique_position_array)
get_sample_reference = Fasta("%s/%s_allele_variants.fa" % (args.filter2_only_snp_vcf_dir, sample_name_re))
if len(get_sample_reference.keys()) == 1:
sample_ref_id = get_sample_reference.keys()
for positions in unique_position_array:
#print positions
#pos_index = unique_position_array.index(positions)
if "/" in str(variant_allele_array_dict[positions]) or len(variant_allele_array_dict[positions]) > 1:
allele_var = str(variant_allele_array_dict[positions][0])
#print allele_var
else:
allele_var = str(variant_allele_array_dict[positions])
# if str(positions) == "1477126":
# print allele_var
ref_allele = str(get_reference.sequence({'chr': str(get_reference.keys()[0]), 'start': int(positions), 'stop': int(positions)}))
generate_vcf_string = "%s\t%s\t.\t%s\t%s\t221.999\t.\t.\t.\t.\n" % (ref_id[0].split(' ')[0], positions, ref_allele, allele_var)
allele_ref_variant_vcf.write(generate_vcf_string)
allele_ref_variant_vcf.close()
filename = "%s/consensus_ref_allele_variant.sh" % args.filter2_only_snp_vcf_dir
vcf_filename = "%s/%s_ref_allele_variants.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re)
f1 = open(filename, 'a+')
bgzip_cmd = "%s/%s/bgzip -f %s\n" % (ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'], vcf_filename)
f1.write(bgzip_cmd)
subprocess.call([bgzip_cmd], shell=True)
tabix_cmd = "%s/%s/tabix -f -p vcf %s.gz\n" % (ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'], vcf_filename)
f1.write(tabix_cmd)
subprocess.call([tabix_cmd], shell=True)
base_vcftools_bin = ConfigSectionMap("bin_path", Config)['binbase'] + "/" + ConfigSectionMap("vcftools", Config)['vcftools_bin']
fasta_cmd = "cat %s | %s/vcf-consensus %s.gz > %s_ref_allele_variants.fa\n" % (args.reference, base_vcftools_bin, vcf_filename, sample_name_re)
f1.write(fasta_cmd)
subprocess.call([fasta_cmd], shell=True)
sed_command = "sed -i 's/>.*/>%s/g' %s_ref_allele_variants.fa\n" % (sample_name_re, sample_name_re)
subprocess.call([sed_command], shell=True)
f1.write(sed_command)
#os.system("bash %s" % filename)
#sequence_lgth_cmd = "for i in %s/*.fa; do %s/%s/bioawk -c fastx \'{ print $name, length($seq) }\' < $i; done" % (args.filter2_only_snp_vcf_dir, ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("bioawk", Config)['bioawk_bin'])
#os.system(sequence_lgth_cmd)
#call("%s" % sequence_lgth_cmd, logger)
unmapped_positions_file = "%s/%s_unmapped.bed_positions" % (args.filter2_only_snp_vcf_dir, os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''))
#print unmapped_positions_file
unmapped_vcf_file = "%s/%s_unmapped.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re)
unmapped_vcf = open(
"%s/%s_unmapped.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
unmapped_vcf.write(vcf_header)
with open(unmapped_positions_file, 'r') as fpp:
for lines in fpp:
lines = lines.strip()
ref_allele = str(get_reference.sequence(
{'chr': str(get_reference.keys()[0]), 'start': int(lines), 'stop': int(lines)}))
generate_vcf_string_unmapped = "%s\t%s\t.\t%s\t-\t221.999\t.\t.\t.\t.\n" % (
ref_id[0].split(' ')[0], lines, ref_allele)
unmapped_vcf.write(generate_vcf_string_unmapped)
unmapped_vcf.close()
bgzip_cmd = "%s/%s/bgzip -f %s\n" % (
ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'],
unmapped_vcf_file)
print bgzip_cmd
tabix_cmd = "%s/%s/tabix -f -p vcf %s.gz\n" % (
ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'],
unmapped_vcf_file)
print tabix_cmd
subprocess.call([bgzip_cmd], shell=True)
subprocess.call([tabix_cmd], shell=True)
#allele_ref_variant_unmapped_vcf = open("%s/%s_ref_allele_variants_unmapped.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re), 'w+')
vcf_filename_unmapped = "%s/%s_ref_allele_unmapped.vcf" % (args.filter2_only_snp_vcf_dir, sample_name_re)
bcftools_merge_cmd = "%s/%s/bcftools merge --merge snps --force-samples %s.gz %s.gz -O v -o %s" % (ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("bcftools", Config)['bcftools_bin'], unmapped_vcf_file, vcf_filename, vcf_filename_unmapped)
bgzip_cmd = "%s/%s/bgzip -f %s\n" % (
ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'],
vcf_filename_unmapped)
subprocess.call([bcftools_merge_cmd], shell=True)
tabix_cmd = "%s/%s/tabix -f -p vcf %s.gz\n" % (
ConfigSectionMap("bin_path", Config)['binbase'], ConfigSectionMap("vcftools", Config)['tabix_bin'],
vcf_filename_unmapped)
fasta_cmd = "cat %s | %s/vcf-consensus %s.gz > %s_ref_allele_unmapped_variants.fa\n" % (
args.reference, base_vcftools_bin, vcf_filename_unmapped, sample_name_re)
#filename = "%s/consensus_ref_allele_unmapped_variant.sh" % args.filter2_only_snp_vcf_dir
filename = "%s/%s_consensus_ref_allele_unmapped_variant.sh" % (args.filter2_only_snp_vcf_dir, sample_name_re)
f1 = open(filename, 'w+')
f1.write(bgzip_cmd)
f1.write(tabix_cmd)
f1.write(fasta_cmd)
print "print here: %s" % filename
subprocess.call(['pwd'], shell=True)
subprocess.call(bgzip_cmd, shell=True)
subprocess.call(tabix_cmd, shell=True)
subprocess.call(fasta_cmd, shell=True)
sed_command = "sed -i 's/>.*/>%s/g' %s_ref_allele_unmapped_variants.fa\n" % (sample_name_re, sample_name_re)
subprocess.call([sed_command], shell=True)
f1.write(sed_command)
f1.close()
else:
print "Sample name %s does not match with column name %s" % (os.path.basename(args.filter2_only_snp_vcf_filename).replace('_filter2_final.vcf_no_proximate_snp.vcf', ''), sample_name_re)
#!/usr/bin/env python
# -*- coding: utf-8 -*-
from pyfasta import Fasta
f = Fasta('test.txt')
print f.keys()
print len(f['X80413'])
print f['X80413'][0:5]
print f.sequence(
{
'chr': 'X80413',
'start': 0,
'stop': len(f[key]),
'strand': '-'
},
one_based=False)
def remove_reads_from_precursor(inbam, outbam, gr, minRlen, readlen_cutoff):
"""
prepare input/output files
"""
inbamPysamObj = pysam.Samfile(inbam, "rb")
outbamPysamObj = pysam.Samfile(outbam, "wb", template=inbamPysamObj)
"""
create genome fetch object
"""
gf = Fasta(gr)
"""
remove reads when 3' has TGG on the genome
"""
for read in inbamPysamObj:
read_name = read.qname
tid = read.rname
readchr = inbamPysamObj.getrname(tid)
readstart = int(read.pos) + 1
readend = read.aend
strand = read.flag
readlen = len(
read.seq) #this is the actual read length (41M, means readlen=41)
read_len = read.qlen #this only considers matches (8S30M, means read_len=30)
if readlen <= readlen_cutoff:
outbamPysamObj.write(read)
continue
# if strand ==0 : #read maps to forward strand
if strand == 0 or strand == 256: #read maps to forward strand
upperlimit = minRlen - readlen
#print(readchr,readend+1,readend+upperlimit)
bpwindow = gf.sequence({
'chr': readchr,
'start': readend + 1,
'stop': readend + upperlimit
})
#print bpwindow
if readlen == minRlen - 1 and (bpwindow == "T" or bpwindow == "A"):
continue #TGGAATTCTCGGGTGCCAAGG
elif readlen == minRlen - 2 and (bpwindow == "TG"
or bpwindow == "AA"):
continue
elif readlen == minRlen - 3 and (bpwindow == "TGG"
or bpwindow == "AAA"):
continue
elif readlen == minRlen - 4 and (bpwindow == "TGGA"
or bpwindow == "AAAA"):
continue
elif readlen == minRlen - 5 and (bpwindow == "TGGAA"
or bpwindow == "AAAAA"):
continue
else:
outbamPysamObj.write(read)
# elif strand ==16: #read maps to reverse strand
elif strand == 16 or strand == 272: #read maps to reverse strand
upperlimit = minRlen - readlen
bpwindow = gf.sequence({
'chr': readchr,
'start': readstart - upperlimit,
'stop': readstart - 1
})
if readlen == minRlen - 1 and (bpwindow == "A" or bpwindow == "T"):
continue #TTCCA
elif readlen == minRlen - 2 and (bpwindow == "CA"
or bpwindow == "TT"):
continue
elif readlen == minRlen - 3 and (bpwindow == "CCA"
or bpwindow == "TTT"):
continue
elif readlen == minRlen - 4 and (bpwindow == "TCCA"
or bpwindow == "TTTT"):
continue
elif readlen == minRlen - 5 and (bpwindow == "TTCCA"
or bpwindow == "TTTTT"):
continue
else:
outbamPysamObj.write(read)
outbamPysamObj.close()
end_index = content.find("-----", start_index)
required_each_content = content[start_index: end_index]
each_motif_lines = required_each_content.strip().split("\n")
for motif_line in each_motif_lines:
splitted = motif_line.split()
chrom1 = splitted[0].split(":")[0]
sequence1 = splitted[5]
strand1 = splitted[1]
if strand1 == "+":
#f.sequence({"chr": "chr18", "start" : (3603155 + 22 -1), "stop" : (3603155 + 22 -1) + len_3, "strand" : "+"}, one_based = False).upper()
# u'TCAGGTCACCAGATAAAG'
start1 = (int(splitted[0].split(":")[1]) + int(splitted[2])) - 1
end1 = start1 + len(sequence1)
seq_pyfasta = f.sequence({"chr": chrom1, "start" : start1, "stop" : end1, "strand" : strand1}, one_based = False).upper()
if strand1 == "-":
#f.sequence({"chr": "chr2", "start" : (112383865 + 59 -1), "stop" : (112383865 + 59 -1) + len_3, "strand" : "-"}, one_based = False).upper()
# u'AATCTTTGTCAGATAATC'
start1 = (int(splitted[0].split(":")[1]) + int(splitted[2])) -1
end1 = start1 + len(sequence1)
seq_pyfasta = f.sequence({"chr": chrom1, "start" : start1, "stop" : end1, "strand" : strand1}, one_based = False).upper()
#convert unicode string to python string
#str(seq_pyfasta)
#seq_pyfasta.encode("ascii", "replace")
#seq_pyfasta.encode("ascii", "ignore")
req = [chrom1, start1, end1, strand1, sequence1, str(seq_pyfasta)]
for i,item in enumerate(req):
class MutateFasta(object):
def __init__(self, fasta):
self.fasta = Fasta(fasta, key_fn=lambda key: key.split()[0])
# self.chroms = [str(i+1) for i in range(22)] + ['X', 'Y'] # , 'MT']
def generate_seq(self, records, offset=None):
if not records and not offset: return
seq = ''
chrom = offset[0] if offset else records[0]['chrom']
prev_pos = offset[1] if offset else 0
last_pos = offset[2] if offset else len(self.fasta[chrom])
for r in records:
ref = self.slice_fasta(r['chrom'], r['pos'], r['pos'])
if not r['chrom'] == chrom: continue
if not (r['ref'] and r['alt']): continue
if not r['ref'][0] == ref: continue
mut_type, sub_seq = self._classify_mut(r['ref'], r['alt'])
if mut_type == 'snv':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'] - 1)
seq += sub_seq
prev_pos = r['pos']
elif mut_type == 'del':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'])
prev_pos += len(sub_seq)
elif mut_type == 'ins':
seq += self.slice_fasta(chrom, prev_pos + 1, r['pos'])
seq += sub_seq
prev_pos = r['pos']
# Reminder
if prev_pos + 1 <= last_pos:
seq += self.slice_fasta(chrom, prev_pos + 1, last_pos)
return seq
def generate_contexted_seq(self, r):
cons = []
chrom = r['chrom']
# TODO: support - strand genes. (currently only supports + strand genes...)
# NOTE: refFlat is stored in 0-based coordinate
# 5'UTR + 1st Exon
cons.append([self.slice_fasta(chrom, r['txStart'] + 1, r['cdsStart']), 'utr'])
cons.append([self.slice_fasta(chrom, r['cdsStart'] + 1, r['exonEnds'][0]), 'exon'])
if r['exonCount'] > 1:
cons.append([self.slice_fasta(chrom, r['exonEnds'][0] + 1, r['exonStarts'][1]), 'intron'])
# Exons
for i,con in enumerate(r['exonStarts']):
if i == 0 or i+1 == r['exonCount']: continue
cons.append([self.slice_fasta(chrom, r['exonStarts'][i] + 1, r['exonEnds'][i]), 'exon'])
cons.append([self.slice_fasta(chrom, r['exonEnds'][i] + 1, r['exonStarts'][i+1]), 'intron'])
# last Exon + 3'UTR
cons.append([self.slice_fasta(chrom, r['exonStarts'][r['exonCount']-1] + 1, r['cdsEnd']), 'exon'])
cons.append([self.slice_fasta(chrom, r['cdsEnd'] + 1, r['txEnd']), 'utr'])
return cons
def slice_fasta(self, chrom, start, stop):
return self.fasta.sequence({'chr': str(chrom), 'start': int(start), 'stop': int(stop)}, one_based=True)
def _classify_mut(self, ref, alt):
"""
>>> _classify_mut('A','G')
('snv', 'G')
>>> _classify_mut('G','GAA')
('ins', 'AA')
>>> _classify_mut('TTA','T')
('del', 'TA')
"""
if len(ref) == len(alt) == 1:
return 'snv', alt
elif len(ref) < len(alt):
assert ref[0] == alt[0], '{0} {1}'.format(ref, alt)
return 'ins', alt[1:]
elif len(ref) > len(alt):
assert ref[0] == alt[0], '{0} {1}'.format(ref, alt)
return 'del', ref[1:]
