def load(self):
load_start(self.datafile)
gene2generif = tab2dict(self.datafile, (1, 2, 4), 0, alwayslist=1)
gene2generif = dict_convert(gene2generif, valuefn=lambda v: {
'generif': [dict(pubmed=self._cvt_pubmed(x[0]), text=x[1]) for x in v]})
load_done('[%d]' % len(gene2generif))
return gene2generif
def _load_ensembl2entrez_li(self):
"""gene_ensembl__xref_entrezgene__dm"""
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__xref_entrezgene__dm.txt')
load_start(DATAFILE)
ensembl2entrez_li = tab2list(DATAFILE, (1, 2), includefn=_not_LRG) # [(ensembl_gid, entrez_gid),...]
load_done('[%d]' % len(ensembl2entrez_li))
self.ensembl2entrez_li = ensembl2entrez_li
def load_ensembl2acc(self):
"""
loading ensembl to transcripts/proteins data
"""
#Loading all ensembl GeneIDs, TranscriptIDs and ProteinIDs
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__translation__main.txt')
load_start(DATAFILE)
ensembl2acc = tab2dict(DATAFILE, (1,2,3), 0, includefn=_not_LRG)
def _fn(x, eid):
out={'gene': eid}
if type(x) is types.ListType:
transcript_li = []
protein_li = []
for _x in x:
if _x[0] and _x[0]!='\\N':
transcript_li.append(_x[0])
if _x[0] and _x[1]!='\\N':
protein_li.append(_x[1])
if transcript_li:
out['transcript']=normalized_value(transcript_li)
if protein_li:
out['protein'] = normalized_value(protein_li)
else:
if x[0] and x[0]!='\\N':
out['transcript'] = x[0]
if x[1] and x[1]!='\\N':
out['protein'] = x[1]
return out
for k in ensembl2acc:
ensembl2acc[k] = {'ensembl': _fn(ensembl2acc[k], k)}
load_done('[%d]' % len(ensembl2acc))
return self.convert2entrez(ensembl2acc)
def loaddata():
#Snowball array
DATAFILE = os.path.join(DATA_FOLDER, 'pigatlas', 'snowball_array_annotation.txt')
load_start(DATAFILE)
gene2snowball = tab2dict(DATAFILE, (0, 1), 1,header=0)
load_done('[%d]' % len(gene2snowball))
return {'snowball': gene2snowball}
def load_cpdb():
print('DATA_FOLDER: '+ DATA_FOLDER)
DATA_FILES = []
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_mouse.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_yeast.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_human.tab'))
arr = {}
for DATA_FILE in DATA_FILES:
load_start(DATA_FILE)
f= open(DATA_FILE,"r")
lines = f.readlines()
for line in lines:
line = line.rstrip('\n')
cols = line.split("\t")
genes = cols[len(cols)-1].split(",")
for gene in genes:
if gene != "entrez_gene_ids" and gene in arr.keys():
if cols[len(cols)-2] not in arr[gene]['pathway'].keys():
arr[gene]['pathway'][cols[len(cols)-2].lower()]={'name':''}
arr[gene]['pathway'][cols[len(cols)-2].lower()]['name'] = cols[len(cols)-4]
if cols[len(cols)-3] != "None":
if cols[len(cols)-2].lower() == "kegg":
arr[gene]['pathway'][cols[len(cols)-2].lower()]['id'] = cols[len(cols)-3].replace("path:","")
else :
arr[gene]['pathway'][cols[len(cols)-2].lower()]['id'] = cols[len(cols)-3]
else:
if cols[len(cols)-3] != "None":
arr[gene]= {'pathway':{cols[len(cols)-2].lower():{'name':cols[len(cols)-4], 'id': cols[len(cols)-3].replace("path:","")}}}
load_done('[%d]' % len(arr))
return arr
def _load_ensembl2entrez_li(self):
"""gene_ensembl__xref_entrezgene__dm"""
CUSTOM_MAPPING_FILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__extra.txt')
if not os.path.exists(CUSTOM_MAPPING_FILE):
print("Missing extra mapping file, now generating")
from . import ensembl_ncbi_mapping
ensembl_ncbi_mapping.main(confirm=False)
load_start(CUSTOM_MAPPING_FILE)
extra = tab2dict(CUSTOM_MAPPING_FILE,(0, 1), 0, alwayslist=True)
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__xref_entrezgene__dm.txt')
load_start(DATAFILE)
ensembl2entrez = tab2dict(DATAFILE, (1, 2), 0, includefn=_not_LRG, alwayslist=True) # [(ensembl_gid, entrez_gid),...]
# replace with our custom mapping
for k in extra:
# when all ensemblIDs are resolved to other EntrezIDs different from those defined in xref file, there can
# be "orphan" EntrezID with no more EnsemblID associated (because there were resolved). Make sure we keep ensembl data
# for those. (so we extend mapping instead of replacing with the ones we previously found)
ensembl2entrez[k].extend(extra[k])
# back to list of tuples
ensembl2entrez_li = []
for ensembl_id, entrez_ids in ensembl2entrez.items():
for entrez_id in entrez_ids:
ensembl2entrez_li.append((ensembl_id, entrez_id))
load_done('[%d]' % len(ensembl2entrez_li))
self.ensembl2entrez_li = ensembl2entrez_li
def load_x(idx, fieldname, cvt_fn=None):
print('DATA_FOLDER: ' + DATA_FOLDER)
DATAFILE = os.path.join(DATA_FOLDER, 'idmapping_selected.tab.gz')
load_start(DATAFILE)
t0 = time.time()
xli = []
for ld in tabfile_feeder(DATAFILE, header=1):
ld = listitems(ld, *(2,19,idx)) # GeneID Ensembl(Gene) target_value
for value in dupline_seperator(dupline=ld,
dup_sep='; '):
xli.append(value)
ensembl2geneid = list2dict(list_nondup([(x[1], x[0]) for x in xli if x[0]!='' and x[1]!='']), 0, alwayslist=True)
xli2 = []
for entrez_id, ensembl_id, x_value in xli:
if x_value:
if cvt_fn:
x_value = cvt_fn(x_value)
if entrez_id:
xli2.append((entrez_id, x_value))
elif ensembl_id:
entrez_id = ensembl2geneid.get(ensembl_id, None)
if entrez_id:
for _eid in entrez_id:
xli2.append((_eid, x_value))
else:
xli2.append((ensembl_id, x_value))
gene2x = list2dict(list_nondup(xli2), 0)
fn = lambda value: {fieldname: sorted(value) if type(value) is types.ListType else value}
gene2x = value_convert(gene2x, fn, traverse_list=False)
load_done('[%d, %s]' % (len(gene2x), timesofar(t0)))
return gene2x
def _load_ensembl2entrez_li(self):
"""gene_ensembl__xref_entrezgene__dm"""
CUSTOM_MAPPING_FILE = os.path.join(DATA_FOLDER,
'gene_ensembl__gene__extra.txt')
if not os.path.exists(CUSTOM_MAPPING_FILE):
print("Missing extra mapping file, now generating")
from . import ensembl_ncbi_mapping
ensembl_ncbi_mapping.main(confirm=False)
load_start(CUSTOM_MAPPING_FILE)
extra = tab2dict(CUSTOM_MAPPING_FILE, (0, 1), 0, alwayslist=True)
DATAFILE = os.path.join(DATA_FOLDER,
'gene_ensembl__xref_entrezgene__dm.txt')
load_start(DATAFILE)
ensembl2entrez = tab2dict(
DATAFILE, (1, 2), 0, includefn=_not_LRG,
alwayslist=True) # [(ensembl_gid, entrez_gid),...]
# replace with our custom mapping
for k in extra:
ensembl2entrez[k] = extra[k]
# back to list of tuples
ensembl2entrez_li = []
for ensembl_id, entrez_ids in ensembl2entrez.items():
for entrez_id in entrez_ids:
ensembl2entrez_li.append((ensembl_id, entrez_id))
load_done('[%d]' % len(ensembl2entrez_li))
self.ensembl2entrez_li = ensembl2entrez_li
def loaddata():
#Snowball array
DATAFILE = os.path.join(DATA_FOLDER, 'pigatlas',
'snowball_array_annotation.txt')
load_start(DATAFILE)
gene2snowball = tab2dict(DATAFILE, (0, 1), 1, header=0)
load_done('[%d]' % len(gene2snowball))
return {'snowball': gene2snowball}
def load_ensembl2pfam(self):
#Prosite
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__prot_pfam__dm.txt')
load_start(DATAFILE)
ensembl2pfam = dict_nodup(tab2dict(DATAFILE, (1, 4), 0))
ensembl2pfam = value_convert(ensembl2pfam, lambda x: {'pfam': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2pfam))
return self.convert2entrez(ensembl2pfam)
def load_ensembl2pfam(self):
#Prosite
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__prot_pfam__dm.txt')
load_start(DATAFILE)
ensembl2pfam = dict_nodup(tab2dict(DATAFILE, (1, 4), 0))
ensembl2pfam = value_convert(ensembl2pfam, lambda x: {'pfam': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2pfam))
return self.convert2entrez(ensembl2pfam)
def load_ensembl2pos(self):
#Genomic position
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__main.txt')
load_start(DATAFILE)
ensembl2pos = dict_nodup(tab2dict(DATAFILE, (1, 3, 4, 5, 6), 0, includefn=_not_LRG))
ensembl2pos = value_convert(ensembl2pos, lambda x: {'chr': x[2], 'start': int(x[0]), 'end': int(x[1]), 'strand': int(x[3])})
ensembl2pos = value_convert(ensembl2pos, lambda x: {'genomic_pos': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2pos))
return self.convert2entrez(ensembl2pos)
def load_ensembl2pos(self):
#Genomic position
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__main.txt')
load_start(DATAFILE)
ensembl2pos = dict_nodup(tab2dict(DATAFILE, (1, 3, 4, 5, 6), 0, includefn=_not_LRG))
ensembl2pos = value_convert(ensembl2pos, lambda x: {'chr': x[2], 'start': int(x[0]), 'end': int(x[1]), 'strand': int(x[3])})
ensembl2pos = value_convert(ensembl2pos, lambda x: {'genomic_pos': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2pos))
return self.convert2entrez(ensembl2pos)
def _load_ensembl_2taxid(self):
"""ensembl2taxid"""
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__translation__main.txt')
load_start(DATAFILE)
ensembl2taxid = dict_nodup(tab2dict(DATAFILE, (0, 1), 1, includefn=_not_LRG))
# need to convert taxid to integer here
ensembl2taxid = value_convert(ensembl2taxid, lambda x: int(x))
load_done('[%d]' % len(ensembl2taxid))
return ensembl2taxid
def load_ensembl2interpro(self):
#Interpro
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__prot_interpro__dm.txt')
load_start(DATAFILE)
ensembl2interpro = dict_nodup(tab2dict(DATAFILE, (1, 4, 5, 6), 0))
ensembl2interpro = value_convert(ensembl2interpro, lambda x: {'id': x[0], 'short_desc': x[1], 'desc': x[2]})
ensembl2interpro = value_convert(ensembl2interpro, lambda x: {'interpro': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2interpro))
return self.convert2entrez(ensembl2interpro)
def _load_ensembl_2taxid(self):
"""ensembl2taxid"""
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__translation__main.txt')
load_start(DATAFILE)
ensembl2taxid = dict_nodup(tab2dict(DATAFILE, (0, 1), 1, includefn=_not_LRG))
# need to convert taxid to integer here
ensembl2taxid = value_convert(ensembl2taxid, lambda x: int(x))
load_done('[%d]' % len(ensembl2taxid))
return ensembl2taxid
def load_ensembl2interpro(self):
#Interpro
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__prot_interpro__dm.txt')
load_start(DATAFILE)
ensembl2interpro = dict_nodup(tab2dict(DATAFILE, (1, 4, 5, 6), 0))
ensembl2interpro = value_convert(ensembl2interpro, lambda x: {'id': x[0], 'short_desc': x[1], 'desc': x[2]})
ensembl2interpro = value_convert(ensembl2interpro, lambda x: {'interpro': x}, traverse_list=False)
load_done('[%d]' % len(ensembl2interpro))
return self.convert2entrez(ensembl2interpro)
def loaddata():
affy_d = {}
for annot in AFFY_ANNOT_FILES:
name = annot['name']
DATAFILE = os.path.join(AFFY_DATA_FOLDER, annot['file'] % AFFY_RELEASE)
load_start(DATAFILE)
d = _load_affy(DATAFILE)
affy_d[name] = d
load_done('[%d]' % len(d))
return affy_d
def loaddata():
affy_d = {}
for annot in AFFY_ANNOT_FILES:
name = annot['name']
DATAFILE = os.path.join(AFFY_DATA_FOLDER, annot['file'] % AFFY_RELEASE)
load_start(DATAFILE)
d = _load_affy(DATAFILE)
affy_d[name] = d
load_done('[%d]' % len(d))
return affy_d
def load_pharmgkb():
print('DATA_FOLDER: ' + DATA_FOLDER)
DATAFILE = os.path.join(DATA_FOLDER, 'genes.zip')
load_start(DATAFILE)
gene2pharmgkb = tab2dict((DATAFILE, 'genes.tsv'), (0, 1), 1, header=1, includefn=lambda ld: ld[1] != '')
fn = lambda value: {'pharmgkb': value}
gene2pharmgkb = value_convert(gene2pharmgkb, fn, traverse_list=False)
load_done('[%d]' % len(gene2pharmgkb))
return gene2pharmgkb
def loaddata():
#GNF1H
DATAFILE = os.path.join(DATA_FOLDER, 'gnf', 'GNF1H.ANNO7.LOAD_20130402.tab')
load_start(DATAFILE)
gene2gnf1h = tab2dict(DATAFILE, (0, 5), 1, header=0, includefn=lambda ld: len(ld) > 5 and ld[5] != '')
load_done('[%d]' % len(gene2gnf1h))
#GNF1m
DATAFILE = os.path.join(DATA_FOLDER, 'gnf', 'gnf1m.NEW_ANNO6.LOAD_20130402.tab')
load_start(DATAFILE)
gene2gnf1m = tab2dict(DATAFILE, (0, 5), 1, header=0, includefn=lambda ld: len(ld) > 5 and ld[5] != '')
load_done('[%d]' % len(gene2gnf1m))
return {'GNF1H': gene2gnf1h,
'GNF1M': gene2gnf1m}
def load(self, aslist=False):
load_start(self.datafile)
print()
geneid_d = get_geneid_d(self.species_li)
gene2unigene = tab2dict(self.datafile, (0, 1), 0, alwayslist=0,
includefn=lambda ld: int(ld[0]) in geneid_d)
gene_d = {}
for gid, unigene in gene2unigene.items():
gene_d[gid] = {'unigene': unigene}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load(self, aslist=False):
load_start(self.datafile)
print()
geneid_d = get_geneid_d(self.species_li)
gene2unigene = tab2dict(self.datafile, (0, 1), 0, alwayslist=0,
includefn=lambda ld: int(ld[0]) in geneid_d)
gene_d = {}
for gid, unigene in gene2unigene.items():
gene_d[gid] = {'unigene': unigene}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load_exons_for_species(species, exons_key='exons'):
refflat_file = os.path.join(DATA_FOLDER, species,
'database/refFlat.txt.gz')
load_start(refflat_file)
t0 = time.time()
ref2exons = {}
for ld in tabfile_feeder(refflat_file, header=0):
refseq = ld[1]
chr = ld[2]
if chr.startswith('chr'):
chr = chr[3:]
exons = list(
zip([int(x) for x in ld[9].split(',') if x],
[int(x) for x in ld[10].split(',') if x]))
assert len(exons) == int(ld[8]), (len(exons), int(ld[8]))
ref2exons.setdefault(refseq, []).append({
'transcript':
refseq,
'chr':
chr,
'strand':
-1 if ld[3] == '-' else 1,
'txstart':
int(ld[4]),
'txend':
int(ld[5]),
'cdsstart':
int(ld[6]),
'cdsend':
int(ld[7]),
'position':
exons
})
gene2exons = {}
for refseq in sorted(ref2exons.keys()):
geneid = refseq2gene.get(refseq, None)
if geneid and geneid != '0':
if geneid not in gene2exons:
gene2exons[geneid] = {exons_key: ref2exons[refseq]}
else:
gene2exons[geneid][exons_key].extend(ref2exons[refseq])
load_done('[%d, %s]' % (len(gene2exons), timesofar(t0)))
return gene2exons
def load_uniprot():
print('DATA_FOLDER: ' + DATA_FOLDER)
DATAFILE = os.path.join(DATA_FOLDER, 'idmapping_selected.tab.gz')
load_start(DATAFILE)
t0 = time.time()
xli = []
for ld in tabfile_feeder(DATAFILE,
header=1,
assert_column_no=VALID_COLUMN_NO):
ld = listitems(ld,
*(0, 1, 2,
18)) # UniProtKB-AC UniProtKB-ID GeneID Ensembl(Gene)
for value in dupline_seperator(
dupline=ld,
dup_idx=[2, 3
], # GeneID and EnsemblID columns may have duplicates
dup_sep='; '):
value = list(value)
value[1] = get_uniprot_section(value[1])
value = tuple(value)
xli.append(value)
ensembl2geneid = list2dict([(x[3], x[2])
for x in xli if x[2] != '' and x[3] != ''],
0,
alwayslist=True)
xli2 = []
for uniprot_acc, section, entrez_id, ensembl_id in xli:
if entrez_id:
xli2.append((uniprot_acc, section, entrez_id))
elif ensembl_id:
entrez_id = ensembl2geneid.get(ensembl_id, None)
if entrez_id:
#if ensembl_id can be mapped to entrez_id
for _eid in entrez_id:
xli2.append((uniprot_acc, section, _eid))
else:
#otherwise, just use ensembl_id
xli2.append((uniprot_acc, section, ensembl_id))
gene2uniprot = list2dict(list_nondup(xli2), 2, alwayslist=True)
gene2uniprot = value_convert(gene2uniprot,
_dict_convert,
traverse_list=False)
load_done('[%d, %s]' % (len(gene2uniprot), timesofar(t0)))
return gene2uniprot
def load_ensembl2acc(self):
"""
loading ensembl to transcripts/proteins data
"""
#Loading all ensembl GeneIDs, TranscriptIDs and ProteinIDs
DATAFILE = os.path.join(DATA_FOLDER,
'gene_ensembl__translation__main.txt')
load_start(DATAFILE)
ensembl2acc = tab2dict(DATAFILE, (1, 2, 3), 0, includefn=_not_LRG)
def _fn(x, eid):
out = {'gene': eid, 'translation': []}
def mapping(transcript_id, protein_id):
trid = transcript_id and transcript_id != '\\N' and transcript_id or None
pid = protein_id and protein_id != '\\N' and protein_id or None
if trid and pid:
out['translation'].append({"rna": trid, "protein": pid})
if isinstance(x, list):
transcript_li = []
protein_li = []
for _x in x:
if _x[0] and _x[0] != '\\N':
transcript_li.append(_x[0])
if _x[1] and _x[1] != '\\N':
protein_li.append(_x[1])
mapping(_x[0], _x[1])
if transcript_li:
out['transcript'] = normalized_value(transcript_li)
if protein_li:
out['protein'] = normalized_value(protein_li)
else:
if x[0] and x[0] != '\\N':
out['transcript'] = x[0]
if x[1] and x[1] != '\\N':
out['protein'] = x[1]
mapping(x[0], x[1])
return out
for k in ensembl2acc:
ensembl2acc[k] = {'ensembl': _fn(ensembl2acc[k], k)}
load_done('[%d]' % len(ensembl2acc))
return self.convert2entrez(ensembl2acc)
def load(self, aslist=False):
load_start(self.datafile)
with file(self.datafile) as df:
geneid_set = set()
doc_li = []
for line in df:
geneid, summary = line.strip().split('\t')
if geneid not in geneid_set:
doc_li.append(dict(_id=geneid, summary=unicode(summary)))
geneid_set.add(geneid)
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def loaddata():
affy_d = {}
for annot in AFFY_ANNOT_FILES:
name = annot['name']
DATAFILE = annot['file']
if DATAFILE.find('%s') != -1:
if DATAFILE.startswith('extra'):
DATAFILE = DATAFILE % AFFY_RELEASE_EXTRA
else:
DATAFILE = DATAFILE % AFFY_RELEASE
DATAFILE = os.path.join(AFFY_DATA_FOLDER, DATAFILE)
load_start(DATAFILE)
d = _load_affy(DATAFILE)
affy_d[name] = d
load_done('[%d]' % len(d))
return affy_d
def load(self, aslist=False):
load_start(self.datafile)
with open(self.datafile) as df:
geneid_set = set()
doc_li = []
for line in df:
geneid, summary = line.strip().split('\t')
if geneid not in geneid_set:
doc_li.append(dict(_id=geneid, summary=str(summary)))
geneid_set.add(geneid)
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def load_cpdb(__metadata__):
# only import pathways from these sources
PATHWAY_SOURCES_INCLUDED = __metadata__['pathway_sources_included']
VALID_COLUMN_NO = 4
t0 = time.time()
print('DATA_FOLDER: ' + DATA_FOLDER)
DATA_FILES = []
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_mouse.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_yeast.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_human.tab'))
_out = []
for DATA_FILE in DATA_FILES:
load_start(DATA_FILE)
for ld in tabfile_feeder(DATA_FILE, header=1, assert_column_no=VALID_COLUMN_NO):
p_name, p_id, p_source = ld[:3]
p_source = p_source.lower()
if p_source == 'kegg' and p_id.startswith('path:'):
p_id = p_id[5:]
if p_source in PATHWAY_SOURCES_INCLUDED:
genes = ld[-1].split(",")
for gene in genes:
_out.append((gene, p_name, p_id, p_source))
load_done()
_out = list2dict(_out, 0, alwayslist=True)
def _inner_cvt(p):
p_name, p_id = p
_d = {'name': p_name}
if p_id != 'None':
_d['id'] = p_id
return _d
def _cvt(pli):
_d = list2dict(pli, 2)
_d = value_convert(_d, _inner_cvt)
for p_source in _d:
if isinstance(_d[p_source], list):
_d[p_source].sort(key=lambda e: e["id"])
return {'pathway': _d}
_out = dict_convert(_out, valuefn=_cvt)
load_done('[%d, %s]' % (len(_out), timesofar(t0)))
return _out
def load(self, aslist=False):
load_start(self.datafile)
gene2go = tab2dict(self.datafile, (1, 2, 3, 4, 5, 6, 7),
0,
alwayslist=1,
includefn=self.species_filter)
category_d = {'Function': 'MF', 'Process': 'BP', 'Component': 'CC'}
def _ff(d):
out = {}
for goid, evidence, qualifier, goterm, pubmed, gocategory in d:
_gocategory = category_d[gocategory]
_d = out.get(_gocategory, [])
_rec = dict(id=goid, term=goterm)
if evidence != '-':
_rec['evidence'] = evidence
if qualifier != '-':
# here I also fixing some inconsistency issues in NCBI data
# Colocalizes_with -> colocalizes_with
# Contributes_with -> contributes_with
# Not -> NOT
_rec['qualifier'] = qualifier.replace('Co', 'co').replace(
'Not', 'NOT')
if pubmed != '-':
if pubmed.find('|') != -1:
pubmed = [int(pid) for pid in pubmed.split('|')]
else:
pubmed = int(pubmed)
_rec['pubmed'] = pubmed
_d.append(_rec)
out[_gocategory] = _d
for k in out:
if len(out[k]) == 1:
out[k] = out[k][0]
return out
gene2go = dict_convert(gene2go, valuefn=_ff)
gene_d = {}
for gid, go in gene2go.items():
gene_d[gid] = {'go': go}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load_cpdb(__metadata__):
# only import pathways from these sources
PATHWAY_SOURCES_INCLUDED = __metadata__['pathway_sources_included']
VALID_COLUMN_NO = 4
t0 = time.time()
print('DATA_FOLDER: ' + DATA_FOLDER)
DATA_FILES = []
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_mouse.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_yeast.tab'))
DATA_FILES.append(os.path.join(DATA_FOLDER, 'CPDB_pathways_genes_human.tab'))
_out = []
for DATA_FILE in DATA_FILES:
load_start(DATA_FILE)
for ld in tabfile_feeder(DATA_FILE, header=1, assert_column_no=VALID_COLUMN_NO):
p_name, p_id, p_source = ld[:3]
p_source = p_source.lower()
if p_source == 'kegg' and p_id.startswith('path:'):
p_id = p_id[5:]
if p_source in PATHWAY_SOURCES_INCLUDED:
genes = ld[-1].split(",")
for gene in genes:
_out.append((gene, p_name, p_id, p_source))
load_done()
_out = list2dict(_out, 0, alwayslist=True)
def _inner_cvt(p):
p_name, p_id = p
_d = {'name': p_name}
if p_id != 'None':
_d['id'] = p_id
return _d
def _cvt(pli):
_d = list2dict(pli, 2)
_d = value_convert(_d, _inner_cvt)
for p_source in _d:
if isinstance(_d[p_source], list):
_d[p_source].sort()
return {'pathway': _d}
_out = dict_convert(_out, valuefn=_cvt)
load_done('[%d, %s]' % (len(_out), timesofar(t0)))
return _out
def _load_ensembl2name(self):
"""loading ensembl gene to symbol+name mapping"""
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__main.txt')
load_start(DATAFILE)
ensembl2name = tab2dict(DATAFILE, (1,2,7), 0, includefn=_not_LRG)
def _fn(x):
out={}
if x[0].strip() not in ['', '\\N']:
out['symbol'] = x[0].strip()
if x[1].strip() not in ['', '\\N']:
_name = SubStr(x[1].strip(), '', ' [Source:').strip()
if _name:
out['name'] = _name
return out
ensembl2name = value_convert(ensembl2name, _fn)
load_done('[%d]' % len(ensembl2name))
return ensembl2name
def load_ensembl2acc(self):
"""
loading ensembl to transcripts/proteins data
"""
#Loading all ensembl GeneIDs, TranscriptIDs and ProteinIDs
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__translation__main.txt')
load_start(DATAFILE)
ensembl2acc = tab2dict(DATAFILE, (1, 2, 3), 0, includefn=_not_LRG)
def _fn(x, eid):
out = {'gene': eid, 'translation' : []}
def mapping(transcript_id, protein_id):
trid = transcript_id and transcript_id != '\\N' and transcript_id or None
pid = protein_id and protein_id != '\\N' and protein_id or None
if trid and pid:
out['translation'].append({"rna" : trid, "protein" : pid})
if isinstance(x, list):
transcript_li = []
protein_li = []
for _x in x:
if _x[0] and _x[0] != '\\N':
transcript_li.append(_x[0])
if _x[1] and _x[1] != '\\N':
protein_li.append(_x[1])
mapping(_x[0],_x[1])
if transcript_li:
out['transcript'] = normalized_value(transcript_li)
if protein_li:
out['protein'] = normalized_value(protein_li)
else:
if x[0] and x[0] != '\\N':
out['transcript'] = x[0]
if x[1] and x[1] != '\\N':
out['protein'] = x[1]
mapping(x[0],x[1])
return out
for k in ensembl2acc:
ensembl2acc[k] = {'ensembl': _fn(ensembl2acc[k], k)}
load_done('[%d]' % len(ensembl2acc))
return self.convert2entrez(ensembl2acc)
def load(self, aslist=False):
load_start(self.datafile)
gene2go = tab2dict(self.datafile, (1, 2, 3, 4, 5, 6, 7), 0, alwayslist=1,
includefn=self.species_filter)
category_d = {'Function': 'MF',
'Process': 'BP',
'Component': 'CC'}
def _ff(d):
out = {}
for goid, evidence, qualifier, goterm, pubmed, gocategory in d:
_gocategory = category_d[gocategory]
_d = out.get(_gocategory, [])
_rec = dict(id=goid, term=goterm)
if evidence != '-':
_rec['evidence'] = evidence
if qualifier != '-':
# here I also fixing some inconsistency issues in NCBI data
# Colocalizes_with -> colocalizes_with
# Contributes_with -> contributes_with
# Not -> NOT
_rec['qualifier'] = qualifier.replace('Co', 'co').replace('Not', 'NOT')
if pubmed != '-':
if pubmed.find('|') != -1:
pubmed = [int(pid) for pid in pubmed.split('|')]
else:
pubmed = int(pubmed)
_rec['pubmed'] = pubmed
_d.append(_rec)
out[_gocategory] = _d
for k in out:
if len(out[k]) == 1:
out[k] = out[k][0]
return out
gene2go = dict_convert(gene2go, valuefn=_ff)
gene_d = {}
for gid, go in gene2go.items():
gene_d[gid] = {'go': go}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load(self, aslist=False):
'''
loading ncbi "homologene.data" file
adding "homologene" field in gene doc
'''
load_start(self.datafile)
with open(self.datafile) as df:
homologene_d = {}
doc_li = []
print()
geneid_d = get_geneid_d(self.species_li)
for line in df:
ld = line.strip().split('\t')
hm_id, tax_id, geneid = [int(x) for x in ld[:3]]
if (self.taxid_set is None or tax_id in self.taxid_set) and \
geneid in geneid_d:
# for selected species only
# and also ignore those geneid does not match any
# existing gene doc
# in case of orignal geneid is retired, replaced with the
# new one, if available.
geneid = geneid_d[geneid]
genes = homologene_d.get(hm_id, [])
genes.append((tax_id, geneid))
homologene_d[hm_id] = genes
doc_li.append(
dict(_id=str(geneid),
taxid=tax_id,
homologene={'id': hm_id}))
for i, gdoc in enumerate(doc_li):
gdoc['homologene']['genes'] = self._sorted_homologenes(
set(homologene_d[gdoc['homologene']['id']]))
doc_li[i] = gdoc
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def _load_ensembl2name(self):
"""loading ensembl gene to symbol+name mapping"""
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__main.txt')
load_start(DATAFILE)
ensembl2name = tab2dict(DATAFILE, (1, 2, 7), 0, includefn=_not_LRG)
def _fn(x):
out = {}
if x[0].strip() not in ['', '\\N']:
out['symbol'] = x[0].strip()
if x[1].strip() not in ['', '\\N']:
_name = SubStr(x[1].strip(), '', ' [Source:').strip()
if _name:
out['name'] = _name
return out
ensembl2name = value_convert(ensembl2name, _fn)
load_done('[%d]' % len(ensembl2name))
return ensembl2name
def load(self, aslist=False):
load_start(self.datafile)
if self.species_li:
_includefn = lambda ld: int(ld[0]) in self.taxid_set and ld[1] != '-'
else:
_includefn = lambda ld: ld[1] != '-'
gene2retired = tab2dict(self.datafile, (1, 2), 0, alwayslist=1,
includefn=_includefn)
gene2retired = dict_convert(gene2retired, valuefn=lambda x: normalized_value([int(xx) for xx in x]))
gene_d = {}
for gid, retired in gene2retired.items():
gene_d[gid] = {'retired': retired}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load(self, aslist=False):
'''
loading ncbi "homologene.data" file
adding "homologene" field in gene doc
'''
load_start(self.datafile)
with open(self.datafile) as df:
homologene_d = {}
doc_li = []
print()
geneid_d = get_geneid_d(self.species_li)
for line in df:
ld = line.strip().split('\t')
hm_id, tax_id, geneid = [int(x) for x in ld[:3]]
if (self.taxid_set is None or tax_id in self.taxid_set) and \
geneid in geneid_d:
# for selected species only
# and also ignore those geneid does not match any
# existing gene doc
# in case of orignal geneid is retired, replaced with the
# new one, if available.
geneid = geneid_d[geneid]
genes = homologene_d.get(hm_id, [])
genes.append((tax_id, geneid))
homologene_d[hm_id] = genes
doc_li.append(dict(_id=str(geneid), taxid=tax_id,
homologene={'id': hm_id}))
for i, gdoc in enumerate(doc_li):
gdoc['homologene']['genes'] = self._sorted_homologenes(
set(homologene_d[gdoc['homologene']['id']]))
doc_li[i] = gdoc
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def load(self, aslist=False):
load_start(self.datafile)
gene2acc = tab2dict(self.datafile, (1, 3, 5, 7), 0, alwayslist=1,
includefn=self.species_filter)
def _ff(d):
out = {
'rna': [],
'protein': [],
'genomic': [],
'translation': []
}
for rna, prot, dna in d:
if rna == '-': rna = None
if prot == '-': prot = None
if dna == '-': dna = None
if rna is not None:
out['rna'].append(rna)
if prot is not None:
out['protein'].append(prot)
if dna is not None:
out['genomic'].append(dna)
if rna and prot:
out['translation'].append({'rna' : rna, 'protein' : prot})
# remove dup
for k in out:
out[k] = normalized_value(out[k])
# remove empty rna/protein/genomic field
_out = {}
for k, v in out.items():
if v:
_out[k] = v
if _out:
_out = {self.fieldname: _out}
return _out
gene2acc = dict_convert(gene2acc, valuefn=_ff)
load_done('[%d]' % len(gene2acc))
if aslist:
return dict_to_list(gene2acc)
else:
return gene2acc
def load(self, aslist=False):
load_start(self.datafile)
if self.species_li:
_includefn = lambda ld: int(ld[0]) in self.taxid_set and ld[1] != '-'
else:
_includefn = lambda ld: ld[1] != '-'
gene2retired = tab2dict(self.datafile, (1, 2), 0, alwayslist=1,
includefn=_includefn)
gene2retired = dict_convert(gene2retired, valuefn=lambda x: normalized_value([int(xx) for xx in x]))
gene_d = {}
for gid, retired in gene2retired.items():
gene_d[gid] = {'retired': retired}
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
def load_ensembl2pos(self):
#Genomic position
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__main.txt')
load_start(DATAFILE)
# Twice 1 because first is the dict key, the second because we need gene id within genomic_pos
ensembl2pos = dict_nodup(
tab2dict(DATAFILE, (1, 1, 3, 4, 5, 6), 0, includefn=_not_LRG))
ensembl2pos = value_convert(
ensembl2pos, lambda x: {
'ensemblgene': x[0],
'chr': x[3],
'start': int(x[1]),
'end': int(x[2]),
'strand': int(x[4])
})
ensembl2pos = value_convert(ensembl2pos,
lambda x: {'genomic_pos': x},
traverse_list=False)
load_done('[%d]' % len(ensembl2pos))
return self.convert2entrez(ensembl2pos)
def load_x(idx, fieldname, cvt_fn=None):
'''idx is 0-based column number'''
print('DATA_FOLDER: ' + DATA_FOLDER)
DATAFILE = os.path.join(DATA_FOLDER, 'idmapping_selected.tab.gz')
load_start(DATAFILE)
t0 = time.time()
xli = []
for ld in tabfile_feeder(DATAFILE,
header=1,
assert_column_no=VALID_COLUMN_NO):
ld = listitems(ld, *(2, 19, idx)) # GeneID Ensembl(Gene) target_value
for value in dupline_seperator(dupline=ld, dup_sep='; '):
xli.append(value)
ensembl2geneid = list2dict(list_nondup([(x[1], x[0]) for x in xli
if x[0] != '' and x[1] != '']),
0,
alwayslist=True)
xli2 = []
for entrez_id, ensembl_id, x_value in xli:
if x_value:
if cvt_fn:
x_value = cvt_fn(x_value)
if entrez_id:
xli2.append((entrez_id, x_value))
elif ensembl_id:
entrez_id = ensembl2geneid.get(ensembl_id, None)
if entrez_id:
for _eid in entrez_id:
xli2.append((_eid, x_value))
else:
xli2.append((ensembl_id, x_value))
gene2x = list2dict(list_nondup(xli2), 0)
fn = lambda value: {
fieldname: sorted(value) if isinstance(value, list) else value
}
gene2x = value_convert(gene2x, fn, traverse_list=False)
load_done('[%d, %s]' % (len(gene2x), timesofar(t0)))
return gene2x
def load_genedoc(self):
"""
Loads gene data from NCBI's refseq2gene.gz file.
Parses it based on genomic position data and refseq status provided by the
list of taxids from get_ref_microbe_taxids() as lookup table
:return:
"""
taxids = loadobj(TAXIDS_FILE)
taxid_set = set(taxids)
load_start(DATAFILE)
def _includefn(ld):
return ld[0] in taxid_set # match taxid from taxid_set
cols_included = [0, 1, 7, 9, 10, 11] # 0-based col idx
gene2genomic_pos_li = tab2list(DATAFILE,
cols_included,
header=1,
includefn=_includefn)
count = 0
last_id = None
for gene in gene2genomic_pos_li:
count += 1
strand = 1 if gene[5] == '+' else -1
_id = gene[1]
mgi_dict = {
'_id': _id,
'genomic_pos': {
'start': int(gene[3]),
'end': int(gene[4]),
'chr': gene[2],
'strand': strand
}
}
if _id != last_id:
# rows with dup _id will be skipped
yield mgi_dict
last_id = _id
load_done('[%d]' % count)
def load_exons_for_species(species, exons_key='exons'):
refflat_file = os.path.join(DATA_FOLDER, species, 'database/refFlat.txt.gz')
reflink_file = os.path.join(DATA_FOLDER, species, 'database/refLink.txt.gz')
load_start(refflat_file)
t0 = time.time()
refseq2gene = tab2dict(reflink_file, (2, 6), 0, alwayslist=False)
ref2exons = []
for ld in tabfile_feeder(refflat_file, header=0):
refseq = ld[1]
chr = ld[2]
if chr.startswith('chr'):
chr = chr[3:]
exons = zip([int(x) for x in ld[9].split(',') if x],
[int(x) for x in ld[10].split(',') if x])
assert len(exons) == int(ld[8]), (len(exons), int(ld[8]))
ref2exons.append((refseq, {
'chr': chr,
'strand': -1 if ld[3] == '-' else 1,
'txstart': int(ld[4]),
'txend': int(ld[5]),
'cdsstart': int(ld[6]),
'cdsend': int(ld[7]),
'exons': exons
}))
ref2exons = list2dict(ref2exons, 0)
gene2exons = {}
for refseq in sorted(ref2exons.keys()):
geneid = refseq2gene.get(refseq, None)
if geneid and geneid != '0':
if geneid not in gene2exons:
gene2exons[geneid] = {exons_key: {refseq: ref2exons[refseq]}}
else:
gene2exons[geneid][exons_key][refseq] = ref2exons[refseq]
load_done('[%d, %s]' % (len(gene2exons), timesofar(t0)))
return gene2exons
def load(self, aslist=False):
load_start(self.datafile)
with open(self.datafile) as df:
geneid_set = set()
doc_li = []
for line in df:
geneid, ec = line.strip().split('\t')
if ec.find(',') != -1:
# there are multiple EC numbers
ec = [str(x) for x in ec.split(',')]
else:
ec = str(ec)
if geneid not in geneid_set:
doc_li.append(dict(_id=geneid, ec=ec))
geneid_set.add(geneid)
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def _load_ensembl2entrez_li(self):
"""gene_ensembl__xref_entrezgene__dm"""
CUSTOM_MAPPING_FILE = os.path.join(DATA_FOLDER, 'gene_ensembl__gene__extra.txt')
if not os.path.exists(CUSTOM_MAPPING_FILE):
print("Missing extra mapping file, now generating")
from . import ensembl_ncbi_mapping
ensembl_ncbi_mapping.main(confirm=False)
load_start(CUSTOM_MAPPING_FILE)
extra = tab2dict(CUSTOM_MAPPING_FILE,(0, 1), 0, alwayslist=True)
DATAFILE = os.path.join(DATA_FOLDER, 'gene_ensembl__xref_entrezgene__dm.txt')
load_start(DATAFILE)
ensembl2entrez = tab2dict(DATAFILE, (1, 2), 0, includefn=_not_LRG, alwayslist=True) # [(ensembl_gid, entrez_gid),...]
# replace with our custom mapping
for k in extra:
ensembl2entrez[k] = extra[k]
# back to list of tuples
ensembl2entrez_li = []
for ensembl_id, entrez_ids in ensembl2entrez.items():
for entrez_id in entrez_ids:
ensembl2entrez_li.append((ensembl_id, entrez_id))
load_done('[%d]' % len(ensembl2entrez_li))
self.ensembl2entrez_li = ensembl2entrez_li
def load_genedoc(self):
"""
Loads gene data from NCBI's refseq2gene.gz file.
Parses it based on genomic position data and refseq status provided by the
list of taxids from get_ref_microbe_taxids() as lookup table
:return:
"""
taxids = loadobj(TAXIDS_FILE)
taxid_set = set(taxids)
load_start(DATAFILE)
def _includefn(ld):
return ld[0] in taxid_set # match taxid from taxid_set
cols_included = [0, 1, 7, 9, 10, 11] # 0-based col idx
gene2genomic_pos_li = tab2list(DATAFILE, cols_included, header=1,
includefn=_includefn)
count = 0
last_id = None
for gene in gene2genomic_pos_li:
count += 1
strand = 1 if gene[5] == '+' else -1
_id = gene[1]
mgi_dict = {
'_id': _id,
'genomic_pos': {
'start': int(gene[3]),
'end': int(gene[4]),
'chr': gene[2],
'strand': strand
}
}
if _id != last_id:
# rows with dup _id will be skipped
yield mgi_dict
last_id = _id
load_done('[%d]' % count)
def load(self, aslist=False):
load_start(self.datafile)
with file(self.datafile) as df:
geneid_set = set()
doc_li = []
for line in df:
geneid, ec = line.strip().split('\t')
if ec.find(',') != -1:
# there are multiple EC numbers
ec = [unicode(x) for x in ec.split(',')]
else:
ec = unicode(ec)
if geneid not in geneid_set:
doc_li.append(dict(_id=geneid, ec=ec))
geneid_set.add(geneid)
load_done('[%d]' % len(doc_li))
if aslist:
return doc_li
else:
gene_d = dict([(d['_id'], d) for d in doc_li])
return gene_d
def load_exons_for_species(species, exons_key='exons'):
refflat_file = os.path.join(DATA_FOLDER, species, 'database/refFlat.txt.gz')
load_start(refflat_file)
t0 = time.time()
ref2exons = {}
for ld in tabfile_feeder(refflat_file, header=0):
refseq = ld[1]
chr = ld[2]
if chr.startswith('chr'):
chr = chr[3:]
exons = list(zip([int(x) for x in ld[9].split(',') if x],
[int(x) for x in ld[10].split(',') if x]))
assert len(exons) == int(ld[8]), (len(exons), int(ld[8]))
ref2exons.setdefault(refseq,[]).append({
'transcript' : refseq,
'chr': chr,
'strand': -1 if ld[3] == '-' else 1,
'txstart': int(ld[4]),
'txend': int(ld[5]),
'cdsstart': int(ld[6]),
'cdsend': int(ld[7]),
'position': exons
})
gene2exons = {}
for refseq in sorted(ref2exons.keys()):
geneid = refseq2gene.get(refseq, None)
if geneid and geneid != '0':
if geneid not in gene2exons:
gene2exons[geneid] = {exons_key: ref2exons[refseq]}
else:
gene2exons[geneid][exons_key].extend(ref2exons[refseq])
load_done('[%d, %s]' % (len(gene2exons), timesofar(t0)))
return gene2exons
def load(self, aslist=False):
load_start(self.datafile)
gene2acc = tab2dict(self.datafile, (1, 3, 5, 7), 0, alwayslist=1,
includefn=self.species_filter)
def _ff(d):
out = {
'rna': [],
'protein': [],
'genomic': []
}
for x1, x2, x3 in d:
if x1 != '-':
out['rna'].append(x1.split('.')[0]) # trim version number after dot
if x2 != '-':
out['protein'].append(x2.split('.')[0])
if x3 != '-':
out['genomic'].append(x3.split('.')[0])
# remove dup
for k in out:
out[k] = normalized_value(out[k])
# remove empty rna/protein/genomic field
_out = {}
for k, v in out.items():
if v:
_out[k] = v
if _out:
_out = {self.fieldname: _out}
return _out
gene2acc = dict_convert(gene2acc, valuefn=_ff)
load_done('[%d]' % len(gene2acc))
if aslist:
return dict_to_list(gene2acc)
else:
return gene2acc
def load_uniprot():
print('DATA_FOLDER: ' + DATA_FOLDER)
DATAFILE = os.path.join(DATA_FOLDER, 'idmapping_selected.tab.gz')
load_start(DATAFILE)
t0 = time.time()
xli = []
for ld in tabfile_feeder(DATAFILE, header=1):
ld = listitems(ld, *(0,1,2,19)) #UniProtKB-AC UniProtKB-ID GeneID Ensembl(Gene)
for value in dupline_seperator(dupline=ld,
dup_idx=[2,3], #GeneID and EnsemblID columns may have duplicates
dup_sep='; '):
value = list(value)
value[1] = get_uniprot_section(value[1])
value = tuple(value)
xli.append(value)
ensembl2geneid = list2dict([(x[3], x[2]) for x in xli if x[2]!='' and x[3]!=''], 0, alwayslist=True)
xli2 = []
for uniprot_acc, section, entrez_id, ensembl_id in xli:
if entrez_id:
xli2.append((uniprot_acc, section, entrez_id))
elif ensembl_id:
entrez_id = ensembl2geneid.get(ensembl_id, None)
if entrez_id:
#if ensembl_id can be mapped to entrez_id
for _eid in entrez_id:
xli2.append((uniprot_acc, section, _eid))
else:
#otherwise, just use ensembl_id
xli2.append((uniprot_acc, section, ensembl_id))
gene2uniprot = list2dict(list_nondup(xli2), 2, alwayslist=True)
gene2uniprot = value_convert(gene2uniprot, _dict_convert, traverse_list=False)
load_done('[%d, %s]' % (len(gene2uniprot), timesofar(t0)))
return gene2uniprot
def get_geneid_d(species_li=None, load_cache=True, save_cache=True):
'''return a dictionary of current/retired geneid to current geneid mapping.
This is useful, when other annotations were mapped to geneids may
contain retired gene ids.
if species_li is None, genes from all species are loaded.
Note that all ids are int type.
'''
if species_li:
taxid_set = set([TAXONOMY[species] for species in species_li])
else:
taxid_set = None
orig_cwd = os.getcwd()
os.chdir(DATA_FOLDER)
# check cache file
_cache_file = 'gene/geneid_d.pyobj'
if load_cache and os.path.exists(_cache_file) and \
file_newer(_cache_file, 'gene/gene_info.gz') and \
file_newer(_cache_file, 'gene/gene_history.gz'):
print('Loading "geneid_d" from cache file...', end='')
_taxid_set, out_d = loadobj(_cache_file)
assert _taxid_set == taxid_set
print('Done.')
os.chdir(orig_cwd)
return out_d
DATAFILE = os.path.join(DATA_FOLDER, 'gene/gene_info.gz')
load_start(DATAFILE)
if species_li:
species_filter = lambda ld: int(ld[0]) in taxid_set
else:
species_filter = None
geneid_li = set(tab2list(DATAFILE, 1, includefn=species_filter))
load_done('[%d]' % len(geneid_li))
DATAFILE = os.path.join(DATA_FOLDER, 'gene/gene_history.gz')
load_start(DATAFILE)
if species_li:
_includefn = lambda ld: int(ld[0]) in taxid_set and ld[1] in geneid_li
else:
_includefn = lambda ld: ld[1] in geneid_li # include all species
retired2gene = tab2dict(DATAFILE, (1, 2),
1,
alwayslist=0,
includefn=_includefn)
# includefn above makes sure taxid is for species_li and filters out those
# mapped_to geneid exists in gene_info list
load_done('[%d]' % len(retired2gene))
# convert key/value to int
out_d = dict_convert(retired2gene, keyfn=int, valuefn=int)
for g in geneid_li:
_g = int(g)
out_d[_g] = _g
if save_cache:
if species_li:
dump((taxid_set, out_d), _cache_file)
else:
dump((None, out_d), _cache_file)
os.chdir(orig_cwd)
return out_d
def load(self, aslist=False):
'''
loading ncbi "gene_info" file
This must be called first to create basic gene documents
with all basic fields, e.g., name, symbol, synonyms, etc.
format of gene_info file:
#Format: tax_id GeneID Symbol LocusTag Synonyms dbXrefs
map_location description type_of_gene Symbol_from
nomenclature_authority Full_name_from_nomenclature_authority
Nomenclature_status Other_designations Modification_da
te (tab is used as a separator, pound sign - start of a comment)
'''
load_start(self.datafile)
gene_d = tab2dict(self.datafile, (0, 1, 2, 3, 4, 5, 7, 8, 9, 13, 14),
key=1,
alwayslist=0,
includefn=self.species_filter)
def _ff(d):
(taxid, symbol, locus_tag, synonyms, dbxrefs, map_location,
description, type_of_gene, other_designations,
modification_date) = d
out = dict(taxid=int(taxid), symbol=symbol, name=description)
if map_location != '-':
out['map_location'] = map_location
if type_of_gene != '-':
out['type_of_gene'] = type_of_gene
if synonyms != '-':
out['alias'] = normalized_value(synonyms.split('|'))
if locus_tag != '-':
out['locus_tag'] = locus_tag
if other_designations != "-":
out['other_names'] = normalized_value(
other_designations.split('|'))
# when merged, this will become the default timestamp
out["_timestamp"] = datetime.datetime.strptime(
modification_date, "%Y%m%d")
for x in dbxrefs.split('|'):
if x == '-':
continue
xd = x.split(':')
if len(xd) == 3 and xd[0] == xd[1] and \
xd[0] in ['VGNC', 'HGNC', 'MGI']:
# a fix for NCBI bug for dup xref prefix, 'HGNC:HGNC:36328'
xd = xd[1:]
try:
_db, _id = xd
except:
print(repr(x))
raise
# we don't need ensembl xref from here, we will get it from
# Ensembl directly
if _db.lower() in ['ensembl', 'imgt/gene-db']:
# we don't need 'IMGT/GENE-DB" xref either, because they
# are mostly the same as gene symbol
continue
# add "MGI:" prefix for MGI ids.
if _db.lower() == 'mgi':
_id = "MGI:" + _id
out[_db] = _id
return out
gene_d = value_convert(gene_d, _ff)
# add entrezgene field
for geneid in gene_d:
d = gene_d[geneid]
d['entrezgene'] = int(geneid)
gene_d[geneid] = d
load_done('[%d]' % len(gene_d))
if aslist:
return dict_to_list(gene_d)
else:
return gene_d
