def distance_comparison(dataframe, data_dir, test_name, samples=10000):
simulated_dir = join(data_dir, test_name)
for index, data in dataframe.iterrows():
lengths = Counter()
inner = []
outer = []
trainsets = glob(join(simulated_dir, index + '*', 'ref_seqs.fasta'))
testsets = glob(join(simulated_dir, index + '*', 'query.fasta'))
for train_fp, test_fp in zip(trainsets, testsets):
train = list(map(str, io.read(train_fp, format='fasta')))
test = list(map(str, io.read(test_fp, format='fasta')))
if not train or not test:
continue
lengths.update(map(len, test))
inner.extend(distances(train, train, samples))
outer.extend(distances(train, test, samples))
inner.sort()
outer.sort()
df = pd.DataFrame({'train/train': inner, 'train/test': outer})
plt.figure() # figsize=(width, height))
ax = regplot('train/train', 'train/test', df, fit_reg=False)
ax.set_title(index, fontsize=20)
maxval = max((inner[-1], outer[-1]))
plt.plot([0, maxval], [0, maxval], linewidth=2)
plt.show()
def main():
parser = argparse.ArgumentParser(
description= 'This script will write out sequences based on \n'
'sequence identifiers in a label file. ',
formatter_class=RawTextHelpFormatter)
req = parser.add_argument_group('REQUIRED')
req.add_argument('-i', '--input_fasta', required=True, action='store',
help='Input fasta file.')
req.add_argument('-l', '--input_sequence_labels', required=True, action='store',
help='File in which the first item in each line is'
' a sequence label / identifier.')
req.add_argument('-o', '--output_fasta', required=True, action='store',
help='Output fasta file.')
optp = parser.add_argument_group('OPTIONAL')
optp.add_argument('-d', '--include_description', action='store_true',
help='Boolean. Keep the additional FASTA header '
'description text.[Default: False]')
optp.add_argument('-r', '--remove_ids', action='store_true',
help='Boolean. Remove sequences with the corresponding '
'IDs, rather than keep. [Default: False]')
p = parser.parse_args()
input_fasta = read(p.input_fasta, format='fasta')
input_labels = open(p.input_sequence_labels, 'U')
output_fasta = open(p.output_fasta, 'w')
remove_ids = p.remove_ids
include_description = p.include_description
seq_labels = parse_labels(input_labels)
filter_seqs(input_fasta, output_fasta, seq_labels, remove_ids=remove_ids,
desc=include_description)
input_fasta.close()
output_fasta.close()
def test_write_genes(self):
genes = sample_genes(self.ortho_groups_fp, min_taxa_cutoff=4.0)
write_genes(genes, self.ref_faa_dir, self.out_fa_dir,
self.out_genes_fp)
# test number of output FASTA files
obs = sorted(listdir(self.out_fa_dir))
exp = sorted(['%s.fa' % ogid for ogid in genes])
self.assertListEqual(obs, exp)
# test output gene list content
with open(self.out_genes_fp, 'r') as f:
obs = f.read()
with open(self.write_genes_list, 'r') as f:
exp = f.read()
self.assertEqual(obs, exp)
# test FASTA file content
for seq in io.read(join(self.out_fa_dir, 'OG0000017.fa'),
format='fasta'):
exp = 'GCF_000160655.1|WP_040356123.1'
self.assertEqual(seq.metadata['id'], exp)
exp = ('MYRKHYAADVTETLDGQTVQVAGWVHRRRDHGGVIFIDLRDRSGLVQIVIDPDTADAF'
'ALAEQVRNEYCLAIEGRVRLRPAGTENPDLASGKIEILGKQLTVLSKSEPLPFQLDED'
'NVSEEIRLKHRTIDLRRDVMQKNLILRSKVAASLRRYLDEHGFMDIETPMLTKATPEG'
'ARDYLVPSRTHPGKFFALPQSPQLFKQMLMMSGFDRYYQIVRCFRDEDLRADRQPEFT'
'QLDIETSFLEEEDILQIMEPMIRGIFKEHLGVELANPFPRMTYREAMRRYASDKPDLR'
'IPLELVDIDDLVKNSGFKVFASVAAQDNGRVVALKIPGGAKLTRKEIDDYTAYVARYG'
'AKGLAYIKVNDATNVEGLQSPIVKFLTTEGGAEGAIALDIIKRVDAQNGDLIFFGADK'
'ASIVNDAIGALRIKVGHDLNMLTCDWAPLWVVDFPMFEYDEKDGRWYSMHHPFTQPKT'
'ANLDELDTNPGDVLSRAYDMVLNGTEIGGGSIRIHRDDMQQRVFKSLGIGAEEAQEKF'
'GFLLNALKYGCPPHGGIAFGLDRLIMLMAGAKSIRDVMAFPKTQTAWCPLTDAPSEAS'
'EAQLRELHIRKRQVEKSE')
self.assertEqual(str(seq), exp)
break
def test_write_genes(self):
genes = sample_genes(self.ortho_groups_fp, min_taxa_cutoff=4.0)
write_genes(genes, self.ref_faa_dir, self.out_fa_dir,
self.out_genes_fp)
# test number of output FASTA files
obs = sorted(listdir(self.out_fa_dir))
exp = sorted(['%s.fa' % ogid for ogid in genes])
self.assertListEqual(obs, exp)
# test output gene list content
with open(self.out_genes_fp, 'r') as f:
obs = f.read()
with open(self.write_genes_list, 'r') as f:
exp = f.read()
self.assertEqual(obs, exp)
# test FASTA file content
for seq in io.read(join(self.out_fa_dir, 'OG0000017.fa'),
format='fasta'):
exp = 'GCF_000160655.1|WP_040356123.1'
self.assertEqual(seq.metadata['id'], exp)
exp = ('MYRKHYAADVTETLDGQTVQVAGWVHRRRDHGGVIFIDLRDRSGLVQIVIDPDTADAF'
'ALAEQVRNEYCLAIEGRVRLRPAGTENPDLASGKIEILGKQLTVLSKSEPLPFQLDED'
'NVSEEIRLKHRTIDLRRDVMQKNLILRSKVAASLRRYLDEHGFMDIETPMLTKATPEG'
'ARDYLVPSRTHPGKFFALPQSPQLFKQMLMMSGFDRYYQIVRCFRDEDLRADRQPEFT'
'QLDIETSFLEEEDILQIMEPMIRGIFKEHLGVELANPFPRMTYREAMRRYASDKPDLR'
'IPLELVDIDDLVKNSGFKVFASVAAQDNGRVVALKIPGGAKLTRKEIDDYTAYVARYG'
'AKGLAYIKVNDATNVEGLQSPIVKFLTTEGGAEGAIALDIIKRVDAQNGDLIFFGADK'
'ASIVNDAIGALRIKVGHDLNMLTCDWAPLWVVDFPMFEYDEKDGRWYSMHHPFTQPKT'
'ANLDELDTNPGDVLSRAYDMVLNGTEIGGGSIRIHRDDMQQRVFKSLGIGAEEAQEKF'
'GFLLNALKYGCPPHGGIAFGLDRLIMLMAGAKSIRDVMAFPKTQTAWCPLTDAPSEAS'
'EAQLRELHIRKRQVEKSE')
self.assertEqual(str(seq), exp)
break
def count_seq(filename):
'''Count seq number in the file.
The file can be gzipped.
'''
for i, s in enumerate(read(filename, format='fasta'), 1):
pass
return i
def mv_seq(seq, opath, name_dict):
seq = read(seq, format='fasta')
with open(opath, 'w') as f1:
for i in seq:
pre_name = i.metadata['id']
i.metadata['id'] = name_dict[pre_name]
i.metadata['description'] = ''
write(i, 'fasta', f1)
def test_compute_gene_score(self):
seqs = get_data_path('pfam.faa')
for number, exp in [(1, 0.1), (102, 1)]:
with NamedTemporaryFile() as faa:
for i, seq in enumerate(read(seqs, format='fasta')):
if i == number:
break
write(seq, into=faa, format='fasta')
faa.flush()
obs = compute_gene_score(faa.name)
self.assertEqual(obs, exp)
def loadRefSeqs(seqsDb, taxRef):
reference_db = []
for e in read(seqsDb, format='fasta', constructor=DNA):
if e.has_degenerates():
# For the purpose of this lesson, we're going to ignore sequences that contain
# degenerate characters (i.e., characters other than A, C, G, or T)
continue
seq_tax = taxRef[e.metadata['id']]
e.metadata['taxonomy'] = seq_tax
reference_db.append(e)
return reference_db
def main():
parser = argparse.ArgumentParser()
parser.add_argument("-i",
"--input_file",
help="location of biom table or fasta file")
parser.add_argument("-o",
"--output_file",
help="location of output biom table or fasta file")
parser.add_argument(
"-f",
"--pynast_fasta",
help="location of pynast failures fasta file to be removed")
args = parser.parse_args()
ids_to_toss = set()
if os.stat(args.pynast_fasta).st_size != 0:
ids_to_toss = set([
i.id for i in read("pynast_aligned_seqs/rep_set_failures.fasta",
format='fasta')
])
if args.input_file.endswith(".biom"):
table = load_table(args.input_file)
set_to_toss = set(table.ids(axis="observation")) & ids_to_toss
table.filter(set_to_toss,
invert=True,
axis="observation",
inplace=True)
table.to_json("remove_pynast_failures.py", open(args.output_file, 'w'))
elif args.input_file.endswith(".fasta") or args.input_file.endswith(".fa"):
if args.output_file is not None:
sys.stdout = open(args.output_file, 'w')
for seq in read(args.input_file, format='fasta'):
if seq.id not in ids_to_toss:
print('>%s\n%s' % (seq.id, str(seq)))
if args.output_file is not None:
sys.stdout.close()
else:
raise ValueError("Input file must of type .biom, .fasta or .fa")
def parse(self):
'''Parse the annotation and add it to interval metadata.
Parameters
----------
fp : str
file path from minced prediction
'''
self.result = {
sid: imd
for sid, imd in read(self.files['gff'], format='gff3')
}
def main():
parser = argparse.ArgumentParser(
description='This script will simply re-write FASTA files '
'without the description. \nWill also convert all Us to Ts and '
'optionally convert "." to "-".'
'That is, this: \n'
'\t>seq1 H. Sapiens\n'
'\tACCGGUUGGCCGUUCAGGGUACAGGUUGGCCGUUCAGGGUAA\n'
'will be output as:\n'
'\t>seq1\n'
'\tACCGGTTGGCCGTTCAGGGTACAGGTTGGCCGTTCAGGGTAA\n'
'Expected to be used with SILVA FASTA files.',
formatter_class=RawTextHelpFormatter)
req = parser.add_argument_group('REQUIRED')
req.add_argument('-i',
'--input_fasta',
required=True,
action='store',
help='Input fasta file.')
req.add_argument('-o',
'--output_fasta',
required=True,
action='store',
help='Output fasta file.')
optp = parser.add_argument_group('OPTIONAL')
optp.add_argument('-d',
'--include_description',
action='store_true',
help='Boolean. Keep the additional FASTA header '
'description text.[Default: False]')
optp.add_argument('-g',
'--convert_to_gap',
action='store_true',
help='Boolean. Convert "." to "-". [Default: False]')
p = parser.parse_args()
input_fasta = read(p.input_fasta, format='fasta')
output_fasta = open(p.output_fasta, 'w')
convert_to_gap = p.convert_to_gap
include_description = p.include_description
parse_seqs(input_fasta,
output_fasta,
convg=convert_to_gap,
desc=include_description)
input_fasta.close()
output_fasta.close()
def load_fasta_ids(path):
"""
Reads sequences from a fasta file and extracts identifiers.
Parameters
----------
input_file : str
fasta file containing contigs and gene identifiers
Returns
-------
List of fasta identifiers
"""
fasta_ids = [seq.metadata['id'] for seq in io.read(path, format='fasta')]
return fasta_ids
def main():
parser = argparse.ArgumentParser(
description='This script will simply degap FASTA files.\n'
'Optionally without the description and or converting '
'Us to Ts.\n'
'That is, this: \n'
'\t>seq1 H. Sapiens\n'
'\t...ACCGGUU---GGCCGUU CAGGGUACAGGUUGGCCGUUCAGGGUAA...\n'
'will be output as:\n'
'\t>seq1\n'
'\tACCGGTTGGCCGTTCAGGGTACAGGTTGGCCGTTCAGGGTAA\n',
formatter_class=RawTextHelpFormatter)
req = parser.add_argument_group('REQUIRED')
req.add_argument('-i',
'--input_fasta',
required=True,
action='store',
help='Input fasta file.')
req.add_argument('-o',
'--output_fasta',
required=True,
action='store',
help='Output fasta file.')
optp = parser.add_argument_group('OPTIONAL')
optp.add_argument('-d',
'--include_description',
action='store_true',
help='Boolean. Keep the additional FASTA header '
'description text.[Default: False]')
optp.add_argument('-u',
'--convert_to_uracil',
action='store_true',
help='Boolean. Convert "U" to "T". [Default: False]')
p = parser.parse_args()
input_fasta = read(p.input_fasta, format='fasta')
output_fasta = open(p.output_fasta, 'w')
convert_to_uracil = p.convert_to_uracil
include_description = p.include_description
parse_seqs(input_fasta,
output_fasta,
convu=convert_to_uracil,
desc=include_description)
input_fasta.close()
output_fasta.close()
def align_sequences(seqs):
import io
from subprocess import run, PIPE
from skbio.io import read, write
from skbio.sequence import Sequence
fasta = 'rational_designs.fa'
seqs = (Sequence(x) for x in seqs)
write(seqs, format='fasta', into=fasta)
clustalo = 'clustalo', '-i', fasta
stdout = run(clustalo, stdout=PIPE, encoding='utf8').stdout
stdout_io = io.StringIO(stdout)
msa = read(stdout_io, format='fasta')
return [str(x) for x in msa]
def parse_msa_file(infile):
"""Read sequences from a multiple sequence alignment (MSA) file.
Parameters
----------
infile : str
file path to input MSA file in A3M format (like FASTA format, but
lowercase letters will be dropped)
Returns
-------
skbio TabularMSA
"""
seqs = []
for seq in io.read(infile, format='fasta'):
seqs.append(Protein(re.sub('[a-z]', '', str(seq)),
metadata=seq.metadata))
return TabularMSA(seqs)
def parse_msa_file(infile):
"""Read sequences from a multiple sequence alignment (MSA) file.
Parameters
----------
infile : str
file path to input MSA file in A3M format (like FASTA format, but
lowercase letters will be dropped)
Returns
-------
skbio TabularMSA
"""
seqs = []
for seq in io.read(infile, format='fasta'):
seqs.append(
Protein(re.sub('[a-z]', '', str(seq)), metadata=seq.metadata))
return TabularMSA(seqs)
def runtime_make_test_data(seqs_in, results_dir, sampling_depths):
'''Repeatedly subsample a fasta sequence file at multiple sequence depths
to generate query/test data for testing method runtimes.
seqs_in: path
fasta format reference sequences.
results_dir: path
Output directory.
sampling_depths: list of integers
Number of sequences to subsample from seqs.
'''
if not exists(results_dir):
makedirs(results_dir)
seqs = [seq for seq in io.read(seqs_in, format='fasta')]
for depth in sampling_depths:
subset = sample(seqs, depth)
tmpfile = join(results_dir, str(depth)) + '.fna'
with open(tmpfile, "w") as output_fasta:
for s in subset:
s.write(output_fasta, format='fasta')
def main():
parser = argparse.ArgumentParser(
description= 'This script will read in a FASTA file and remove '
'any sequences that have homopolymers and ambiguous base calls.'
'That is, the following sequences would be removed: \n'
'\t>seq1-homopolymeric\n'
'\tACCGGTTGGCCGTTTTTTTTTCAGGGMACAGGTTVGCCGTTCAGGGTAA\n'
'\t>seq2-ambiguos-bases\n'
'\tACCGGTTGGCCVTGCCGMMTTCVVAGRGTAY\n',
formatter_class=RawTextHelpFormatter)
req = parser.add_argument_group('REQUIRED')
req.add_argument('-i', '--input_fasta', required=True, action='store',
help='Input fasta file.')
req.add_argument('-o', '--output_fasta', required=True, action='store',
help='Output fasta file.')
optp = parser.add_argument_group('OPTIONAL')
optp.add_argument('-p', '--n_homopolymer_length', action='store',
type=int, default=8,
help='Remove sequences that contain homopolymers of '
'greater than or equal to length n. \n'
"[Default %(default)s)]")
optp.add_argument('-a', '--n_ambiguous_bases', action='store', type=int,
default=5, help='Remove sequences that contain a '
'number of IUPAC ambiguous bases greater than or equal '
"to length n. \n[Default %(default)s)]")
p = parser.parse_args()
input_fasta = read(p.input_fasta, format='fasta')
output_fasta = open(p.output_fasta, 'w')
n_homopolymer_length = p.n_homopolymer_length
n_ambiguous_bases = p.n_ambiguous_bases
filter_seqs(input_fasta, output_fasta,
n_homopolymer_length=n_homopolymer_length,
n_ambiguous_bases=n_ambiguous_bases)
input_fasta.close()
output_fasta.close()
def extract_sequences(infile, seqidx=0):
""" Extract sequence(s) from a multi-sequence FASTA file
Parameters
----------
infile : str
file path to input multi-sequence FASTA file
seqidx : int (optional)
n-th sequence of the input file to extract
(default: 0 for all sequences)
Returns
-------
list of skbio Sequence
"""
seqs = []
iseq = 0 # current sequence index
for seq in io.read(infile, format='fasta'):
iseq += 1
if 0 < seqidx != iseq:
continue
seqs.append(seq)
return seqs
def make_tRNA_table(mature_fa,
tRNA_structure,
tRNA_fa,
tablename,
prefix='TR'):
tRNA_dict = tRNA_seq_dict(mature_fa)
anticodon_dict = anticodon_pos(tRNA_structure)
rows = []
for record in read(tRNA_fa, 'fasta'):
if record.metadata['id'].startswith(prefix):
tRNA_id = tRNA_dict[str(record)]
anticodon = record.metadata['id'].split('-')[1]
pos, annotated_anticodon, aa = anticodon_dict[tRNA_id].split(',')
tRNA_length = len(record)
rows.append(
(record.metadata['id'], 0, tRNA_length, anticodon, pos, aa,
str(record)))
df = pd.DataFrame(rows, columns = ['tRNA','start','end','anticodon','anticodon_pos', 'aa', 'seq']) \
.assign(anticodon_start = lambda d: d.anticodon_pos.str.extract('^([0-9]+)-',expand=False).astype(int))\
.assign(anticodon_end = lambda d: d.anticodon_pos.str.extract('-([0-9]+)$',expand=False).astype(int)) \
.assign(predicted_anticodon = lambda d: list(map(lambda x,y,z: x[(y-1):z], d.seq, d.anticodon_start, d.anticodon_end)))\
.to_csv(tablename, sep='\t', index=False)
print('Written %s' % tablename)
def parse(self):
'''Parse the annotation and add it to interval metadata.'''
self.result = {
sid: imd
for sid, imd in read(self.files['gff'], format='gff3')
}
def tRNA_seq_dict(mature_fa):
tRNA_dict = {}
for r in read(mature_fa, 'fasta'):
description = r.metadata['description'].split(' ')[2].strip(')')
tRNA_dict[str(r).replace('U', 'T') + 'CCAA'] = description
return tRNA_dict
def tax_acc(argv):
"""Computing accuracy of taxonomic classification across all ranks"""
parser = argparse.ArgumentParser()
parser.add_argument('lca',
type=str,
help='aggregated ORF LCA output. See agg-orf command')
parser.add_argument(
'taxonomy',
type=str,
help='the preprocessed GTDB taxonomy file. See prep-meta command')
parser.add_argument('fasta',
type=str,
help='the input Fasta file with genomic sequences')
parser.add_argument('-o',
'--output',
type=str,
help='the output file to save results to',
default=None)
args = parser.parse_args(argv)
logger = get_logger()
seqs = list()
accs = list()
for seq in skio.read(args.fasta, format='fasta'):
accession, length, seq_name = seq.metadata['id'].split('-')
seqs.append(seq_name)
accs.append(accession)
input_df = pd.DataFrame({'accession': accs, 'seq_name': seqs})
# accession,domain,phylum,class,order,family,genus,species,gtdb_genome_representative
logger.info(f'Reading taxonomy from {args.taxonomy}')
taxdf = pd.read_csv(args.taxonomy, index_col='accession')
ar122 = (taxdf['domain'] == 'd__Archaea').values
bac120 = (taxdf['domain'] == 'd__Bacteria').values
logger.info(
f' - found {ar122.sum()} Archaea genomes and {bac120.sum()} Bacteria genomes'
)
# accession,seq_name,domain,phylum,class,order,family,genus,species
# GCA_000380905.1,AQYW01000001.1,d__Archaea,p__Nanoarchaeota,c__Nanoarchaeia,o__SCGC-AAA011-G17,f__SCGC-AAA011-G17,g__SCGC-AAA011-G17,s__SCGC-AAA011-G17 sp000402515
logger.info(f'Reading LCA results from {args.lca}')
lca_df = pd.read_csv(args.lca)
lca_df = input_df.set_index('seq_name').join(
lca_df.set_index('seq_name').drop('accession', axis=1))
taxdf = taxdf.filter(lca_df['accession'], axis=0)
results = {
'accuracy': list(),
'pclfd': list(),
'bac_accuracy': list(),
'bac_pclfd': list(),
'ar_accuracy': list(),
'ar_pclfd': list()
}
ar122 = (taxdf['domain'] == 'd__Archaea').values
bac120 = (taxdf['domain'] == 'd__Bacteria').values
logger.info(
f' - found {ar122.sum()} Archaea sequences and {bac120.sum()} Bacteria sequences'
)
ar122_tax = taxdf.index[ar122]
bac120_tax = taxdf.index[bac120]
logger.info(
f' - found {len(set(ar122_tax))} Archaea genomes and {len(set(bac120_tax))} Bacteria genomes'
)
def get_results(tdf, ldf, col, sub=None):
if sub is not None:
tdf = tdf.iloc[sub]
ldf = ldf.iloc[sub]
mask = ldf[col].notna().values
true = tdf[col][mask].values
pred = ldf[col][mask].values
eq = true == pred
return mask.mean(), eq.mean()
for col in taxlevels[1:]:
logger.info(f'computing results for {col}')
pclfd, acc = get_results(taxdf, lca_df, col)
results['pclfd'].append(pclfd)
results['accuracy'].append(acc)
pclfd, acc = get_results(taxdf, lca_df, col, sub=bac120)
results['bac_pclfd'].append(pclfd)
results['bac_accuracy'].append(acc)
pclfd, acc = get_results(taxdf, lca_df, col, sub=ar122)
results['ar_pclfd'].append(pclfd)
results['ar_accuracy'].append(acc)
df = pd.DataFrame(data=results, index=taxlevels[1:])
if args.output is not None:
df.to_csv(args.output)
print(df)
def write_genes(genes, input_faa_dir, output_fa_dir, output_genes_fp):
""" Write protein sequences of selected gene families to external files
Parameters
----------
genes : dict of dict of set of str
{ ogid : { taxon : set(protein(s)) }
return value of sample_genes or filter_paralogs
input_faa_dir : str
directory of input protein sequences from the query genome and the
selected taxa for comparison (FASTA format, one taxon per file)
output_fa_dir : str
directory to store output protein sequences (FASTA format, one gene
family per file)
output_genes_fp : str
file to store a list of selected gene families and their members.
format: gene1<tab>taxon1|protein1,taxon2|protein2,...
"""
# generate a taxon to protein to gene family map
# so complicated because it is optimized for subsequent filesystem I/O
prots = {}
for ogid in genes:
for taxon in genes[ogid]:
if taxon not in prots:
prots[taxon] = {}
for prot in genes[ogid][taxon]:
if prot in prots[taxon]:
prots[taxon][prot].add(ogid)
else:
prots[taxon][prot] = set([ogid])
# match taxa with faa filenames
# so complicated because OrthoFinder trims off the version number from
# an NCBI-style accession (e.g., GCF_012345.1 becomes GCF_012345)
taxon2file = {}
for fname in os.listdir(input_faa_dir):
if fname.endswith('.faa'):
taxon = fname.split('.')[0]
if taxon in prots:
taxon2file[taxon] = fname
# read protein sequences
seqs = {}
for taxon in taxon2file:
for seq in io.read(os.path.join(input_faa_dir, taxon2file[taxon]),
format='fasta'):
id = seq.metadata['id']
if id in prots[taxon]:
seqs[id] = str(seq)
# write protein sequences per selected gene family
for ogid in sorted(genes):
members = []
with open(os.path.join(output_fa_dir, '%s.fa' % ogid), 'w') as f:
for taxon in sorted(genes[ogid]):
# restore taxon name from OrthoFinder-crippled form
trutax = taxon2file[taxon][:-4]
for prot in sorted(genes[ogid][taxon]):
if prot in seqs:
# sequence IDs are like: taxon|protein
f.write('>%s|%s\n%s\n' % (trutax, prot, seqs[prot]))
members.append('%s|%s' % (trutax, prot))
with open(output_genes_fp, 'a') as f:
f.write('%s\t%s\n' % (ogid, ','.join(members)))
if len(sys.argv) == 1:
parser.print_help()
sys.exit(1)
args = parser.parse_args()
logging.basicConfig(stream=sys.stdout,
level=logging.DEBUG,
format='%(asctime)s - %(message)s')
logger = logging.getLogger()
logger.info('loading data %s' % args.input)
io = get_hdf5io(args.input, 'r')
difile = io.read()
difile.set_raw()
tid = difile.seq_table[args.idx][3][1]
sid = difile.seq_table[args.idx][1]
fofin = open(args.fof, 'r')
for line in map(lambda x: x.strip(), fofin):
if tid in line:
fasta_file = line
break
fofin.close()
print(sid, tid, fasta_file)
for seq in skbio.io.read(fasta_file, constructor=Protein, format='fasta'):
if sid == seq.metadata['id']:
import argparse
import os
import sys
from skbio import DNA
import skbio.io as skio
desc = "fasta_path must be a file path from NCBI and have the genome assembly accession in it"
parser = argparse.ArgumentParser(description=desc)
parser.add_argument('fasta_path', type=str, help='the fasta file to append the prefix to')
args = parser.parse_args()
args.prefix = os.path.basename(args.fasta_path)[:15]
seqs = list()
tmp_fa = sys.stdout
w = 100
for seq in skio.read(args.fasta_path, format='fasta', constructor=DNA):
seq.metadata['id'] = args.prefix+"-"+str(len(seq))+"-"+seq.metadata['id']
seqs.append(seq)
tmp_fa.write('>')
tmp_fa.write(seq.metadata['id'])
tmp_fa.write('\n')
for s in range(0, len(seq), w):
tmp_fa.write(''.join(seq.values[s:s+w].astype('U')))
tmp_fa.write('\n')
def mt_tRNA_tab(mature_fa):
rows = []
for record in read(mature_fa, 'fasta'):
rows.append((record.metadata['id'], str(record), 0, len(str(record))))
return pd.DataFrame(rows, columns=['tRNA', 'seq', 'start', 'end'])
def write_genes(genes,
input_faa_dir,
output_fa_dir,
output_genes_fp):
""" Write protein sequences of selected gene families to external files
Parameters
----------
genes : dict of dict of set of str
{ ogid : { taxon : set(protein(s)) }
return value of sample_genes or filter_paralogs
input_faa_dir : str
directory of input protein sequences from the query genome and the
selected taxa for comparison (FASTA format, one taxon per file)
output_fa_dir : str
directory to store output protein sequences (FASTA format, one gene
family per file)
output_genes_fp : str
file to store a list of selected gene families and their members.
format: gene1<tab>taxon1|protein1,taxon2|protein2,...
"""
# generate a taxon to protein to gene family map
# so complicated because it is optimized for subsequent filesystem I/O
prots = {}
for ogid in genes:
for taxon in genes[ogid]:
if taxon not in prots:
prots[taxon] = {}
for prot in genes[ogid][taxon]:
if prot in prots[taxon]:
prots[taxon][prot].add(ogid)
else:
prots[taxon][prot] = set([ogid])
# match taxa with faa filenames
# so complicated because OrthoFinder trims off the version number from
# an NCBI-style accession (e.g., GCF_012345.1 becomes GCF_012345)
taxon2file = {}
for fname in os.listdir(input_faa_dir):
if fname.endswith('.faa'):
taxon = fname.split('.')[0]
if taxon in prots:
taxon2file[taxon] = fname
# read protein sequences
seqs = {}
for taxon in taxon2file:
for seq in io.read(os.path.join(input_faa_dir, taxon2file[taxon]),
format='fasta'):
id = seq.metadata['id']
if id in prots[taxon]:
seqs[id] = str(seq)
# write protein sequences per selected gene family
for ogid in sorted(genes):
members = []
with open(os.path.join(output_fa_dir, '%s.fa' % ogid), 'w') as f:
for taxon in sorted(genes[ogid]):
# restore taxon name from OrthoFinder-crippled form
trutax = taxon2file[taxon][:-4]
for prot in sorted(genes[ogid][taxon]):
if prot in seqs:
# sequence IDs are like: taxon|protein
f.write('>%s|%s\n%s\n' % (trutax, prot, seqs[prot]))
members.append('%s|%s' % (trutax, prot))
with open(output_genes_fp, 'a') as f:
f.write('%s\t%s\n' % (ogid, ','.join(members)))
def main():
parser = argparse.ArgumentParser(
description='Using a minimum sequence length per taxonomic '
'group. \nThis script will read in a FASTA file and a taxonomy file, '
'\nany sequence that does not fit the length criteria for a given '
'\ntaxonomic group will be discarded. For example, if the following '
'\ncriteria are specified:\n'
'\n\t\'{"d__Bacteria":1200, "d__Archaea":900}\'\n'
'\nThis means, any Bacterial and Eukaryal sequences less than 1200 '
'\nbases, and any Archaeal sequences less than 900 bases, will be '
'\ndiscarded.',
formatter_class=RawTextHelpFormatter)
req = parser.add_argument_group('REQUIRED')
req.add_argument('-i',
'--input_sequences',
required=True,
action='store',
help='Input fasta file.')
req.add_argument('-t',
'--input_taxonomy',
required=True,
action='store',
help='Input taxonomy file.')
req.add_argument('-o',
'--output_sequences',
required=True,
action='store',
help='Output filtered FASTA file.')
optp = parser.add_argument_group('OPTIONAL')
optp.add_argument(
'-g',
'--taxonomic_groups',
action='store',
default='{"d__Bacteria":1200, "d__Archaea":900, "d__Eukaryota":1400}',
help='List of taxonomic groups and associated minimum seq '
'\nlength. Any sequences greater than or equal to length n.'
'\nTip: set to \'{}\' if you only want to use the '
'\n\'global_length_min\' option.'
"\n[Default: \'%(default)s\']")
optp.add_argument(
'-m',
'--global_length_min',
action='store',
default='1200',
type=int,
help='Any taxonomic groups not specified, will have their '
'\nsequences discarded if they do not fit this length '
'\ncritera. Set to large value if you want to remove all '
'\nunspecified taxonomic groups.'
"groups.\n[Default: %(default)s]")
p = parser.parse_args()
input_sequences = read(p.input_sequences, format='fasta')
output_sequences = open(p.output_sequences, 'w')
input_taxonomy = open(p.input_taxonomy, 'U')
taxonomic_groups = p.taxonomic_groups
global_length_min = p.global_length_min
id_taxonomy_dict = make_taxonomy_dict(input_taxonomy)
taxonomic_groups_dict = make_tax_group_dict(taxonomic_groups)
filter_seqs_by_len_and_tax(input_sequences,
output_sequences,
taxonomic_groups_dict,
id_taxonomy_dict,
global_length_min=global_length_min)
input_sequences.close()
output_sequences.close()
current = t.ids('observation')
updated = map(lambda x: x.upper(), current)
if len(set(updated)) != len(updated):
print('************>', a.id, fp, '<**************')
if set(current) ^ set(updated):
print('Changing biom: ', a.id, fp)
t.update_ids({i: i.upper() for i in t.ids('observation')},
axis='observation', inplace=True)
with biom_open(fp, 'w') as f:
t.to_hdf5(f, t.generated_by)
checksum = compute_checksum(fp)
elif fpt == 'preprocessed_fasta':
changed = False
tmp = fp + '.tmp'
with open(tmp, 'w') as out:
for seq in read(fp, format='fasta'):
seq = str(seq)
sequ = seq.upper()
out.write('>%s\n%s\n' % (sequ, sequ))
if seq != sequ:
changed = True
if changed:
print('Changing biom: ', a.id, fp)
rename(tmp, fp)
checksum = compute_checksum(fp)
else:
remove(tmp)
if checksum is not None:
TRN.add(sql, [checksum, _id])
TRN.execute()
def extract_sequences(infile, identifiers=None):
"""Extract sequence(s) from a multi-sequence FASTA file.
Parameters
----------
infile : str
file path to input multi-sequence FASTA file
identifiers :
int
sequence index (n-th sequence in the file)
str
sequence ID (name) or index
numeric str is treated as index instead of ID
comma-separated sequence IDs or indexes
file path to sequence list (one ID or index per line)
sequence index range as "start..end" (both included)
start must be smaller or equal to end
list of int
sequence indexes
list of str
sequence IDs or indexes
tuple of two int's
sequence index range as (start, end)
if omitted, all sequences will be extracted
Returns
-------
list of skbio Sequence
extracted protein sequences
Raises
------
ValueError
if tuple (index range) is not in (start, end) form
if index range str is not formatted as "start, end"
if the data type of identifiers is incorrect
"""
l, ids, indexes = [], set(), set()
if identifiers:
# IDs or indexes as list
if isinstance(identifiers, list):
l = identifiers
# start and end indexes as tuple of int
elif isinstance(identifiers, tuple):
if len(identifiers) == 2 \
and all(isinstance(n, int) for n in identifiers) \
and 0 < identifiers[0] <= identifiers[1]:
l = list(range(identifiers[0], identifiers[1] + 1))
else:
raise ValueError('Error: Index range must be a tuple of '
'(start, end).')
elif isinstance(identifiers, str):
# read from a file
if os.path.isfile(identifiers):
with open(identifiers, 'r') as f:
l = f.read().splitlines()
# start and end indexes as str
elif '..' in identifiers:
l = identifiers.split('..')
if len(l) == 2 \
and all(n.isdigit() for n in l) \
and 0 < int(l[0]) <= int(l[1]):
l = list(range(int(l[0]), int(l[1]) + 1))
else:
raise ValueError('Error: Index range must be formatted as '
'"start..end".')
# IDs or indexes as str (single or comma-separated list)
else:
l = list(map(str.strip, identifiers.split(',')))
# index as int
elif isinstance(identifiers, int):
l = [identifiers]
else:
raise ValueError('Error: Incorrect data type of identifiers.')
for i in l:
if isinstance(i, int): # index of this protein in the file
indexes.add(i)
elif i.isdigit():
indexes.add(int(i))
else:
ids.add(i) # protein ID (name)
seqs = []
for i, seq in enumerate(io.read(infile, format='fasta')):
if ids:
if seq.metadata['id'] in ids:
seqs.append(seq)
elif indexes:
if i + 1 in indexes: # indexes start with 1, not 0
seqs.append(seq)
else:
seqs.append(seq)
return seqs
#!/usr/bin/env python
import RNA
from skbio import io
import re
import sys
if len(sys.argv) != 2:
sys.exit('[usage] python %s <fasta file>' % sys.argv[0])
fa = sys.argv[1]
for r in io.read(fa, 'fasta'):
seq = str(r)[20:-20]
f, e = RNA.fold(seq.strip('N'))
folded = RNA.b2C(f)
is_cloverleave = re.findall('[A-Z]', folded)
is_tRNA = is_cloverleave and 'HHH' in ''.join(is_cloverleave)
closed_end = folded.startswith('(') and folded.endswith(')')
cloverleave = 'cloverleaf' if is_tRNA and closed_end else 'hairpin'
print(r.metadata['id'], cloverleave, folded, seq.strip('N'))
def generate_cross_validated_sequences(read_taxa, simulated_reads_fp, index,
iterations, cv_dir):
'''Generates simulated community files (fasta and taxonomy) as subsets of
simulated amplicons/taxa for cross-validated taxonomy assignment. Selects
duplicated taxa names, evenly allocates these among subsets as query taxa
(test set), generates ref taxa (training set) that do not match query fasta
IDs, and creates fasta files to match each of these sets.
read_taxa: list or path
list or file of taxonomies corresponding to simulated_reads_fp
simulated_reads_fp: path
simulated amplicon reads (fasta format file)
index: str
reference database name
iterations: int >= 2
number of subsets to create
cv_dir: path
base output directory to contain simulated datasets
'''
if iterations < 2:
raise ValueError('Must perform two or more iterations for '
'construction of cross-validated datasets.')
# Stratify the data and form the CV data sets
simulated_reads = list(io.read(simulated_reads_fp, format='fasta'))
taxonomy = Artifact.import_data('FeatureData[Taxonomy]',
read_taxa,
view_type='HeaderlessTSVTaxonomyFormat')
tree = build_tree(taxonomy, simulated_reads)
strata = get_strata(tree, iterations)
print(index + ': generating', iterations, 'folds on', len(strata),
'strata')
X, y = zip(*[(s, t) for t, ss in strata for s in ss])
skf = StratifiedKFold(n_splits=iterations, shuffle=True, random_state=0)
splits = []
for train, test in skf.split(X, y):
train_set = {X[i] for i in train}
test_set = {X[i] for i in test}
splits.append((train_set, test_set))
# Output the CV data sets in the expected formats
taxonomy_series = taxonomy.view(pd.Series)
for iteration, (train, test) in enumerate(splits):
db_iter_dir = join(cv_dir, '{0}-iter{1}'.format(index, iteration))
if not exists(db_iter_dir):
makedirs(db_iter_dir)
query_taxa_fp = join(db_iter_dir, 'query_taxa.tsv')
query_fp = join(db_iter_dir, 'query.fasta')
ref_fp = join(db_iter_dir, 'ref_seqs.fasta')
ref_taxa_fp = join(db_iter_dir, 'ref_taxa.tsv')
# Output the taxa files
train_series = taxonomy_series[train]
train_series.to_csv(ref_taxa_fp, sep='\t')
# If a taxonomy in the test set doesn't exist in the training set, trim
# it until it does
train_taxonomies = set()
for taxonomy in train_series.values:
taxonomy = taxonomy.split(';')
for level in range(1, len(taxonomy) + 1):
train_taxonomies.add(';'.join(taxonomy[:level]))
test_list = []
for sid in test:
taxonomy = taxonomy_series[sid].split(';')
for level in range(len(taxonomy), 0, -1):
if ';'.join(taxonomy[:level]) in train_taxonomies:
test_list.append('\t'.join(
[sid, ';'.join(taxonomy[:level]).strip()]))
break
else:
raise RuntimeError('unknown kingdom in query set')
export_list_to_file(test_list, query_taxa_fp)
# Output the reference files
with open(ref_fp, 'w') as ref_fasta:
with open(query_fp, 'w') as query_fasta:
for seq in simulated_reads:
if seq.metadata['id'] in train:
seq.write(ref_fasta, format='fasta')
else:
seq.write(query_fasta, format='fasta')
# Encode as Artifacts for convenience
artifact = Artifact.import_data('FeatureData[Sequence]', ref_fp)
artifact.save(ref_fp[:-5] + 'qza')
artifact = Artifact.import_data('FeatureData[Sequence]', query_fp)
artifact.save(query_fp[:-5] + 'qza')
artifact = Artifact.import_data(
'FeatureData[Taxonomy]',
ref_taxa_fp,
view_type='HeaderlessTSVTaxonomyFormat')
artifact.save(ref_taxa_fp[:-3] + 'qza')
from skbio.io import read, write
seqs = read("example.fna", qual="example.qual", format="fasta")
write(seqs, into="example.fastq", variant="illumina1.8", format="fastq")
def summarize_blast6(filename):
df = read(filename, format="blast+6", into=pd.DataFrame, default_columns=True)
df_best = filter_best(df)
def loadTree(tree): with open(tree, 'r') as f: tree = read(f, format="newick", into=TreeNode) return tree
def extract_sequences(infile, identifiers=None):
"""Extract sequence(s) from a multi-sequence FASTA file.
Parameters
----------
infile : str
file path to input multi-sequence FASTA file
identifiers :
int
sequence index (n-th sequence in the file)
str
sequence ID (name) or index
numeric str is treated as index instead of ID
comma-separated sequence IDs or indexes
file path to sequence list (one ID or index per line)
sequence index range as "start..end" (both included)
start must be smaller or equal to end
list of int
sequence indexes
list of str
sequence IDs or indexes
tuple of two int's
sequence index range as (start, end)
if omitted, all sequences will be extracted
Returns
-------
list of skbio Sequence
extracted protein sequences
Raises
------
ValueError
if tuple (index range) is not in (start, end) form
if index range str is not formatted as "start, end"
if the data type of identifiers is incorrect
"""
l, ids, indexes = [], set(), set()
if identifiers:
# IDs or indexes as list
if isinstance(identifiers, list):
l = identifiers
# start and end indexes as tuple of int
elif isinstance(identifiers, tuple):
if len(identifiers) == 2 \
and all(isinstance(n, int) for n in identifiers) \
and 0 < identifiers[0] <= identifiers[1]:
l = list(range(identifiers[0], identifiers[1] + 1))
else:
raise ValueError('Error: Index range must be a tuple of '
'(start, end).')
elif isinstance(identifiers, str):
# read from a file
if os.path.isfile(identifiers):
with open(identifiers, 'r') as f:
l = f.read().splitlines()
# start and end indexes as str
elif '..' in identifiers:
l = identifiers.split('..')
if len(l) == 2 \
and all(n.isdigit() for n in l) \
and 0 < int(l[0]) <= int(l[1]):
l = list(range(int(l[0]), int(l[1]) + 1))
else:
raise ValueError('Error: Index range must be formatted as '
'"start..end".')
# IDs or indexes as str (single or comma-separated list)
else:
l = list(map(str.strip, identifiers.split(',')))
# index as int
elif isinstance(identifiers, int):
l = [identifiers]
else:
raise ValueError('Error: Incorrect data type of identifiers.')
for i in l:
if isinstance(i, int): # index of this protein in the file
indexes.add(i)
elif i.isdigit():
indexes.add(int(i))
else:
ids.add(i) # protein ID (name)
seqs = []
for i, seq in enumerate(io.read(infile, format='fasta')):
if ids:
if seq.metadata['id'] in ids:
seqs.append(seq)
elif indexes:
if i+1 in indexes: # indexes start with 1, not 0
seqs.append(seq)
else:
seqs.append(seq)
return seqs