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864 lines (775 loc) · 29.3 KB
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#!/usr/bin/env python
import os
import contextlib
import sys
import sqlalchemy as sql
from sqlalchemy.orm import mapper, create_session
import sqlalchemy
from ped import get_ped_fields
def index_variation(cursor):
cursor.execute('''create index var_chr_start_idx on\
variants(chrom, start)''')
cursor.execute('''create index var_type_idx on variants(type)''')
cursor.execute('''create index var_gt_counts_idx on \
variants(num_hom_ref, num_het, \
num_hom_alt, num_unknown)''')
cursor.execute('''create index var_aaf_idx on variants(aaf)''')
cursor.execute('''create index var_in_dbsnp_idx on variants(in_dbsnp)''')
cursor.execute('''create index var_in_call_rate_idx on variants(call_rate)''')
cursor.execute('''create index var_exonic_idx on variants(is_exonic)''')
cursor.execute('''create index var_coding_idx on variants(is_coding)''')
cursor.execute('''create index var_lof_idx on variants(is_lof)''')
cursor.execute('''create index var_som_idx on variants(is_somatic)''')
cursor.execute('''create index var_depth_idx on variants(depth)''')
cursor.execute('''create index var_gene_idx on variants(gene)''')
cursor.execute('''create index var_trans_idx on variants(transcript)''')
cursor.execute('''create index var_impact_idx on variants(impact)''')
cursor.execute('''create index var_impact_severity_idx on variants(impact_severity)''')
cursor.execute('''create index var_esp_idx on variants(aaf_esp_all)''')
cursor.execute('''create index var_1kg_idx on variants(aaf_1kg_all)''')
cursor.execute('''create index var_qual_idx on variants(qual)''')
cursor.execute('''create index var_homref_idx on variants(num_hom_ref)''')
cursor.execute('''create index var_homalt_idx on variants(num_hom_alt)''')
cursor.execute('''create index var_het_idx on variants(num_het)''')
cursor.execute('''create index var_unk_idx on variants(num_unknown)''')
cursor.execute('''create index var_omim_idx on variants(in_omim)''')
cursor.execute('''create index var_cadd_raw_idx on variants(cadd_raw)''')
cursor.execute('''create index var_cadd_scaled_idx on variants(cadd_scaled)''')
cursor.execute('''create index var_fitcons_idx on variants(fitcons)''')
cursor.execute('''create index chrom_varid_idx on variants(chrom,variant_id)''')
cursor.execute('CREATE index max_aaf_all_idx on variants(max_aaf_all)')
def index_variation_impacts(cursor):
cursor.execute('''create index varimp_exonic_idx on \
variant_impacts(is_exonic)''')
cursor.execute('''create index varimp_coding_idx on \
variant_impacts(is_coding)''')
cursor.execute(
'''create index varimp_lof_idx on variant_impacts(is_lof)''')
cursor.execute('''create index varimp_impact_idx on \
variant_impacts(impact)''')
cursor.execute('''create index varimp_trans_idx on \
variant_impacts(transcript)''')
cursor.execute('''create index varimp_gene_idx on \
variant_impacts(gene)''')
def index_samples(cursor):
cursor.execute('''create unique index sample_name_idx on samples(name)''')
def index_gene_detailed(cursor):
cursor.execute('''create index gendet_chrom_gene_idx on \
gene_detailed(chrom, gene)''')
cursor.execute('''create index gendet_rvis_idx on \
gene_detailed(rvis_pct)''')
cursor.execute('''create index gendet_transcript_idx on \
gene_detailed(transcript)''')
cursor.execute('''create index gendet_ccds_idx on \
gene_detailed(ccds_id)''')
def index_gene_summary(cursor):
cursor.execute('''create index gensum_chrom_gene_idx on \
gene_summary(chrom, gene)''')
cursor.execute('''create index gensum_rvis_idx on \
gene_summary(rvis_pct)''')
def create_indices(cursor):
"""
Index our master DB tables for speed
"""
index_variation(cursor)
index_variation_impacts(cursor)
index_samples(cursor)
index_gene_detailed(cursor)
index_gene_summary(cursor)
def create_gene_view(cursor):
"""
View of gene_summary table, without redundances
"""
cursor.execute('''create view gene_view as \
SELECT * from gene_summary group by ensembl_gene_id having count(*)=1
UNION
SELECT * from gene_summary where is_hgnc=='1' group by ensembl_gene_id having count(*)>1
''')
def get_path(path):
if "://" not in path:
if not (os.path.exists(path) or os.access(os.path.dirname(os.path.abspath(path)), os.W_OK)):
raise Exception("unable to find path: %s" % path)
path = "sqlite:///%s" % path
return path
def create_tables(path, effect_fields=None):
"""
Create our master DB tables
"""
if effect_fields:
effect_string = "".join(e + (" float,\n" if e.endswith("_num") else " TEXT,\n") for e in effect_fields)
else:
effect_string = ""
db = dict(variants="""
chrom varchar(15),
start integer,
end integer,
vcf_id text,
variant_id integer,
anno_id integer,
ref text,
alt text,
qual float,
filter text,
type varchar(15),
sub_type text,
gts blob,
gt_types blob,
gt_phases blob,
gt_depths blob,
gt_ref_depths blob,
gt_alt_depths blob,
gt_quals blob,
gt_copy_numbers blob,
gt_phred_ll_homref blob,
gt_phred_ll_het blob,
gt_phred_ll_homalt blob,
call_rate float,
max_aaf_all float,
in_dbsnp bool,
rs_ids text default NULL,
sv_cipos_start_left integer,
sv_cipos_end_left integer,
sv_cipos_start_right integer,
sv_cipos_end_right integer,
sv_length integer,
sv_is_precise bool,
sv_tool text,
sv_evidence_type text,
sv_event_id text,
sv_mate_id text,
sv_strand text,
in_omim bool,
clinvar_sig text default NULL,
clinvar_disease_name text default NULL,
clinvar_dbsource text default NULL,
clinvar_dbsource_id text default NULL,
clinvar_origin text default NULL,
clinvar_dsdb text default NULL,
clinvar_dsdbid text default NULL,
clinvar_disease_acc text default NULL,
clinvar_in_locus_spec_db bool,
clinvar_on_diag_assay bool,
clinvar_causal_allele text,
clinvar_gene_phenotype text,
geno2mp_hpo_ct integer,
pfam_domain text,
cyto_band text default NULL,
rmsk text default NULL,
in_cpg_island bool,
in_segdup bool,
is_conserved bool,
gerp_bp_score float,
gerp_element_pval float,
num_hom_ref integer,
num_het integer,
num_hom_alt integer,
num_unknown integer,
aaf real,
hwe decimal(2,7),
inbreeding_coeff decimal(2,7),
pi decimal(2,7),
recomb_rate decimal(2,7),
gene varchar(60),
transcript varchar(60),
is_exonic bool,
is_coding bool,
is_splicing bool,
is_lof bool,
exon text,
codon_change text,
aa_change text,
aa_length text,
biotype text,
impact varchar(60) default NULL,
impact_so text default NULL,
impact_severity varchar(15),
polyphen_pred text,
polyphen_score float,
sift_pred text,
sift_score float,
anc_allele text,
rms_bq float,
cigar text,
depth integer default NULL,
strand_bias float default NULL,
rms_map_qual float default NULL,
in_hom_run integer default NULL,
num_mapq_zero integer default NULL,
num_alleles integer default NULL,
num_reads_w_dels float default NULL,
haplotype_score float default NULL,
qual_depth float default NULL,
allele_count integer default NULL,
allele_bal float default NULL,
in_hm2 bool,
in_hm3 bool,
is_somatic bool,
somatic_score float,
in_esp bool,
aaf_esp_ea decimal(2,7),
aaf_esp_aa decimal(2,7),
aaf_esp_all decimal(2,7),
exome_chip bool,
in_1kg bool,
aaf_1kg_amr decimal(2,7),
aaf_1kg_eas decimal(2,7),
aaf_1kg_sas decimal(2,7),
aaf_1kg_afr decimal(2,7),
aaf_1kg_eur decimal(2,7),
aaf_1kg_all decimal(2,7),
grc text default NULL,
gms_illumina float,
gms_solid float,
gms_iontorrent float,
in_cse bool,
encode_tfbs text,
encode_dnaseI_cell_count integer,
encode_dnaseI_cell_list text,
encode_consensus_gm12878 text,
encode_consensus_h1hesc text,
encode_consensus_helas3 text,
encode_consensus_hepg2 text,
encode_consensus_huvec text,
encode_consensus_k562 text,
vista_enhancers text,
cosmic_ids text,
info blob,
cadd_raw float,
cadd_scaled float,
fitcons float,
in_exac bool,
aaf_exac_all decimal(2,7),
aaf_adj_exac_all decimal(2,7),
aaf_adj_exac_afr decimal(2,7),
aaf_adj_exac_amr decimal(2,7),
aaf_adj_exac_eas decimal(2,7),
aaf_adj_exac_fin decimal(2,7),
aaf_adj_exac_nfe decimal(2,7),
aaf_adj_exac_oth decimal(2,7),
aaf_adj_exac_sas decimal(2,7),
exac_num_het int,
exac_num_hom_alt int,
exac_num_chroms int,
%s""" % effect_string.rstrip(","),
variants_cnv = """
variant_id integer,
chrom varchar(15),
start integer,
end integer,
ref text,
alt text,
type varchar(15),
genotype varchar(15),
sub_type text,
gts blob,
gt_types blob,
gt_phases blob,
gt_depths blob,
gt_ref_depths blob,
gt_alt_depths blob,
gt_quals blob,
gt_copy_numbers blob,
gt_phred_ll_homref blob,
gt_phred_ll_het blob,
gt_phred_ll_homalt blob,
sv_cipos_start_left integer,
sv_cipos_end_left integer,
sv_cipos_start_right integer,
sv_cipos_end_right integer,
sv_length integer,
sv_is_precise bool,
sv_tool text,
sv_evidence_type text,
sv_event_id text,
sv_mate_id text,
sv_strand text,
in_cpg_island bool,
in_segdup bool,
is_conserved bool,
cyto_band text default NULL,
rmsk text default NULL,
recomb_rate decimal(2,7),
fitcons float,
encode_tfbs text,
encode_dnaseI_cell_count integer,
encode_dnaseI_cell_list text,
%s""" % effect_string.rstrip(","),
variant_impacts="""
variant_id integer,
anno_id integer,
gene varchar(60),
transcript varchar(60),
is_exonic bool,
is_coding bool,
is_lof bool,
exon text,
codon_change text,
aa_change text,
aa_length text,
biotype text,
impact varchar(60),
impact_so text,
impact_severity varchar(15),
polyphen_pred text,
polyphen_score float,
sift_pred text,
sift_score float,
%s""" % effect_string.rstrip(","),
sample_genotypes="""
sample_id integer,
gt_types BLOB""",
sample_genotype_counts="""
sample_id integer,
num_hom_ref integer,
num_het integer,
num_hom_alt integer,
num_unknown integer""",
resources="""
name text,
resource text""",
version="""version text""",
gene_detailed="""
uid integer,
chrom varchar(60),
gene varchar(60),
is_hgnc bool,
ensembl_gene_id text,
transcript varchar(60),
biotype text,
transcript_status text,
ccds_id varchar(60),
hgnc_id text,
entrez_id text,
cds_length text,
protein_length text,
transcript_start text,
transcript_end text,
strand text,
synonym text,
rvis_pct float,
mam_phenotype_id text""",
gene_summary="""
uid integer,
chrom varchar(60),
gene varchar(60),
is_hgnc bool,
ensembl_gene_id text,
hgnc_id text,
transcript_min_start integer,
transcript_max_end integer,
strand text,
synonym text,
rvis_pct float,
mam_phenotype_id text,
in_cosmic_census bool,
""",
vcf_header="""vcf_header text""",
)
# in the future this will be replaced by reading from the conf file.
lookup = {'real': sql.Float(),
'float': sql.Float(),
'text': sql.Text(),
'bool': sql.Boolean(),
'blob': sql.LargeBinary(),
'decimal(2,7)': sql.Float(), #sql.DECIMAL(precision=7, scale=2, asdecimal=False),
'integer': sql.Integer(),
'varchar(15)': sql.String(20),
'varchar(60)': sql.String(60),
'int': sql.Integer(),
}
for table in db:
db[table] = db[table].strip().strip(",").split(",\n")
db[table] = [x.strip().split() for x in db[table]]
cols = [sql.Column(c[0], lookup[c[1].lower()]) for c in db[table]]
if table != "variant_impacts":
for c in cols:
if c.name in ("variant_id", "sample_id", "uid"):
c.primary_key = True
if c.name == "variant_id" and table == "variants":
c.autoincrement = False
db[table] = cols
e = sql.create_engine(get_path(path), isolation_level=None)
e.connect().connection.connection.text_factory = str
metadata = sql.MetaData(bind=e)
session = create_session(bind=e, autocommit=False, autoflush=False)
mapped = {}
tables = ['variants'] + [x for x in sorted(db) if x != 'variants']
otables = [sql.Table(tbl, metadata, *db[tbl]) for tbl in tables]
metadata.drop_all(tables=otables)
for t in otables:
mapped[t.name] = t
session.commit()
metadata.create_all()
return session, metadata
def create_sample_table(cursor, metadata, args):
NUM_BUILT_IN = 6
cols = [sql.Column("sample_id", sql.Integer, primary_key=True)]
fields = get_ped_fields(args.ped_file)
optional_fields = ["family_id", "name", "paternal_id", "maternal_id",
"sex", "phenotype"]
optional_fields += fields[NUM_BUILT_IN:]
for field in optional_fields:
if field == "name":
cols.append(sql.Column(field, sql.String(50)))
else:
cols.append(sql.Column(field, sql.TEXT))
t = sql.Table("samples", metadata, *cols)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_dgv_table(cursor, metadata, args):
cols = [sql.Column("uid",sql.Integer, primary_key = True),
sql.Column("chr",sql.TEXT),
sql.Column("start",sql.Integer),
sql.Column("end", sql.Integer),
sql.Column("state", sql.TEXT),
sql.Column("id", sql.Text),
sql.Column("type", sql.TEXT),
sql.Column("num_variants", sql.Integer),
sql.Column("num_samples", sql.Integer),
sql.Column("num_samples_multicounted", sql.Integer),
sql.Column("num_studies", sql.Integer),
sql.Column("variants", sql.TEXT),
sql.Column("samples", sql.TEXT),
sql.Column("studies", sql.TEXT),
sql.Column("African", sql.Integer),
sql.Column("Asian", sql.Integer),
sql.Column("European", sql.Integer),
sql.Column("Mexican", sql.Integer),
sql.Column("Middle_east", sql.Integer),
sql.Column("Native_american", sql.Integer),
sql.Column("Oceania", sql.Integer),
sql.Column("South_american", sql.Integer),]
t = sql.Table("dgv_map", metadata, *cols, extend_existing = True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_cnv_map(cursor, metadata, args):
cols = [sql.Column("uid",sql.Integer,primary_key=True),
sql.Column("chr",sql.TEXT),
sql.Column("start",sql.Integer),
sql.Column("end", sql.Integer),
sql.Column("opt_field", sql.TEXT)]
t = sql.Table("cnv_map", metadata, *cols, extend_existing = True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_gene_custom_table(cursor,metadata,args):
cols = [sql.Column("uid", sql.Integer, primary_key=True),
sql.Column("chrom", sql.TEXT),
sql.Column("transcript_min_start", sql.Integer),
sql.Column("transcript_max_end", sql.Integer),
sql.Column("gene", sql.TEXT)]
t = sql.Table("gene_custom_map", metadata, *cols,extend_existing=True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_overlap_result(cursor,metadata,args):
cols = [sql.Column("uid",sql.Integer, primary_key=True),
sql.Column("chrom_A",sql.TEXT),
sql.Column("start_A",sql.Integer),
sql.Column("end_A",sql.Integer),
sql.Column("len_A",sql.Integer),
sql.Column("overlap_A_perc", sql.TEXT),
sql.Column("alt",sql.TEXT),
sql.Column("chrom_B",sql.TEXT),
sql.Column("start_B",sql.Integer),
sql.Column("end_B", sql.Integer),
sql.Column("len_B", sql.Integer),
sql.Column("overlap_B_perc", sql.TEXT),
sql.Column("type", sql.TEXT),
sql.Column("overlap_bp", sql.Integer),
sql.Column("jaccard_index", sql.Float),
sql.Column("num_variants", sql.Integer),
sql.Column("num_samples", sql.Integer),
sql.Column("African", sql.Integer),
sql.Column("Asian", sql.Integer),
sql.Column("European", sql.Integer),
sql.Column("Mexican", sql.Integer),
sql.Column("Middle_east", sql.Integer),
sql.Column("Native_american", sql.Integer),
sql.Column("Oceania", sql.Integer),
sql.Column("South_american", sql.Integer),
sql.Column("gts",sql.LargeBinary()),
sql.Column("gt_types",sql.LargeBinary()),
sql.Column("gt_phases",sql.LargeBinary()),
sql.Column("gt_depths",sql.LargeBinary()),
sql.Column("gt_ref_depths",sql.LargeBinary()),
sql.Column("gt_alt_depths",sql.LargeBinary()),
sql.Column("gt_quals",sql.LargeBinary()),
sql.Column("gt_copy_numbers",sql.LargeBinary()),
sql.Column("gt_phred_ll_homref",sql.LargeBinary()),
sql.Column("gt_phred_ll_het",sql.LargeBinary()),
sql.Column("gt_phred_ll_homalt",sql.LargeBinary())]
t = sql.Table("overlap", metadata, *cols,extend_existing=True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_no_overlap_result(cursor,metadata,args):
# table for result of no overlap intersect
cols = [sql.Column("uid",sql.Integer, primary_key=True),
sql.Column("chrom", sql.TEXT),
sql.Column("start", sql.Integer),
sql.Column("end", sql.Integer),
sql.Column("len",sql.Integer),
sql.Column("alt", sql.TEXT),
sql.Column("gts",sql.LargeBinary()),
sql.Column("gt_types",sql.LargeBinary()),
sql.Column("gt_phases",sql.LargeBinary()),
sql.Column("gt_depths",sql.LargeBinary()),
sql.Column("gt_ref_depths",sql.LargeBinary()),
sql.Column("gt_alt_depths",sql.LargeBinary()),
sql.Column("gt_quals",sql.LargeBinary()),
sql.Column("gt_copy_numbers",sql.LargeBinary()),
sql.Column("gt_phred_ll_homref",sql.LargeBinary()),
sql.Column("gt_phred_ll_het",sql.LargeBinary()),
sql.Column("gt_phred_ll_homalt",sql.LargeBinary())
]
t = sql.Table("no_overlap", metadata, *cols,extend_existing=True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_overlap_custom_result(cursor, metadata, args):
cols = [sql.Column("uid",sql.Integer, primary_key=True),
sql.Column("chrom_A",sql.TEXT),
sql.Column("start_A",sql.Integer),
sql.Column("end_A",sql.Integer),
sql.Column("len_A",sql.Integer),
sql.Column("overlap_A_perc", sql.TEXT),
sql.Column("alt",sql.TEXT),
sql.Column("chrom_B",sql.TEXT),
sql.Column("start_B",sql.Integer),
sql.Column("end_B", sql.Integer),
sql.Column("len_B", sql.Integer),
sql.Column("overlap_B_perc", sql.TEXT),
sql.Column("opt_field",sql.TEXT),
sql.Column("overlap_bp", sql.Integer),
sql.Column("jaccard_index", sql.Float),sql.Column("gts",sql.LargeBinary()),
sql.Column("gt_types",sql.LargeBinary()),
sql.Column("gt_phases",sql.LargeBinary()),
sql.Column("gt_depths",sql.LargeBinary()),
sql.Column("gt_ref_depths",sql.LargeBinary()),
sql.Column("gt_alt_depths",sql.LargeBinary()),
sql.Column("gt_quals",sql.LargeBinary()),
sql.Column("gt_copy_numbers",sql.LargeBinary()),
sql.Column("gt_phred_ll_homref",sql.LargeBinary()),
sql.Column("gt_phred_ll_het",sql.LargeBinary()),
sql.Column("gt_phred_ll_homalt",sql.LargeBinary())]
t = sql.Table('overlap_custom', metadata, *cols,extend_existing=True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def create_gene_overlap_result(cursor, metadata, args):
cols = [sql.Column("uid", sql.Integer, primary_key=True),
sql.Column("variant_id",sql.Integer),
sql.Column("chrom",sql.TEXT),
sql.Column("type",sql.TEXT),
sql.Column("sub_type",sql.TEXT),
sql.Column("alt",sql.TEXT),
sql.Column("sv_length", sql.Integer),
sql.Column("start", sql.Integer),
sql.Column("end", sql.Integer),
sql.Column("gene", sql.TEXT),
sql.Column("transcript_min_start", sql.Integer),
sql.Column("transcript_max_end", sql.Integer),
sql.Column("perc", sql.Float),
sql.Column("gts",sql.LargeBinary()),
sql.Column("gt_types",sql.LargeBinary()),
sql.Column("gt_phases",sql.LargeBinary()),
sql.Column("gt_depths",sql.LargeBinary()),
sql.Column("gt_ref_depths",sql.LargeBinary()),
sql.Column("gt_alt_depths",sql.LargeBinary()),
sql.Column("gt_quals",sql.LargeBinary()),
sql.Column("gt_copy_numbers",sql.LargeBinary()),
sql.Column("gt_phred_ll_homref",sql.LargeBinary()),
sql.Column("gt_phred_ll_het",sql.LargeBinary()),
sql.Column("gt_phred_ll_homalt",sql.LargeBinary())]
t = sql.Table('overlap_gene_result',metadata, *cols,extend_existing = True)
t.drop(checkfirst=True)
metadata.create_all(tables=[t])
def insert_variation(session, metadata, buffer):
"""
Populate the variants table with each variant in the buffer.
"""
if len(buffer) == 0: return
tbl = metadata.tables['variants']
cols = _get_cols(tbl)
left = set(cols) - set(buffer[0].keys())
assert len(left) == 0, left
left = set(buffer[0].keys()) - set(cols)
assert len(left) == 0, left
try:
session.execute(tbl.insert(), buffer)
session.commit()
except:
sys.stderr.write("insert error trying 1 at a time:\n")
session.rollback()
stmt = tbl.insert()
with session.bind.begin() as trans:
for b in buffer:
trans.execute(stmt, b)
raise
def insert_variation_cnv(session, metadata, buffer):
"""
Populate the CNV variants table with each variant in the buffer.
"""
if len(buffer) == 0: return
tbl = metadata.tables['variants_cnv']
cols = _get_cols(tbl)
left = set(cols) - set(buffer[0].keys())
assert len(left) == 0, left
left = set(buffer[0].keys()) - set(cols)
assert len(left) == 0, left
try:
session.execute(tbl.insert(), buffer)
session.commit()
except:
sys.stderr.write("insert error trying 1 at a time:\n")
session.rollback()
stmt = tbl.insert()
with session.bind.begin() as trans:
for b in buffer:
trans.execute(stmt, b)
raise
def insert_variation_impacts(session, metadata, buffer):
"""
Populate the variant_impacts table with each variant in the buffer.
"""
if len(buffer) == 0: return
tbl = metadata.tables['variant_impacts']
session.execute(tbl.insert(), buffer)
session.commit()
def insert_sample(session, metadata, sample_list):
"""
Populate the samples with sample ids, names, and
other indicative information.
"""
tbl = metadata.tables['samples']
cols = [c.key for c in tbl.c]
session.execute(tbl.insert(), dict(zip(cols, sample_list)))
def _get_cols(tbl):
return [c.key for c in tbl.c]
def gen_gene_vals(cols, table_contents):
for row in table_contents:
d = dict(zip(cols, row))
d['is_hgnc'] = bool(d['is_hgnc'] != '0')
if d['rvis_pct'] in (None, 'None'):
d['rvis_pct'] = None
else:
d['rvis_pct'] = float(d['rvis_pct'])
if "in_cosmic_census" in d:
d['in_cosmic_census'] = bool(d['in_cosmic_census'])
yield d
def insert_gene_detailed(session, metadata, table_contents):
t = metadata.tables['gene_detailed']
cols = _get_cols(t)
n = 1000
for chunk in (table_contents[i:i+n] for i in xrange(0, len(table_contents), n)):
session.execute(t.insert(), list(gen_gene_vals(cols, chunk)))
def insert_gene_summary(session, metadata, contents):
t = metadata.tables['gene_summary']
cols = _get_cols(t)
session.execute(t.insert(), list(gen_gene_vals(cols, contents)))
session.commit()
def insert_resources(session, metadata, resources):
"""Populate table of annotation resources used in this database.
"""
t = metadata.tables['resources']
cols = _get_cols(t)
session.execute(t.insert(), [dict(zip(cols, r)) for r in resources])
session.commit()
def insert_vcf_header(session, metadata, vcf_header):
"""Populate a table storing the original VCF header.
"""
t = metadata.tables['vcf_header']
session.execute(t.insert(), dict(vcf_header=vcf_header.rstrip("\r\n")))
session.commit()
def insert_version(session, metadata, version):
"""Populate table of documenting which
gemini version was used for this database.
"""
t = metadata.tables['version']
session.execute(t.insert(), dict(version=version))
session.commit()
def gen_map(cols,table_contents):
for row in table_contents:
d = dict(zip(cols,row))
yield d
def insert_dgv_map(session, metadata, dgvmap):
"""Populate table of DGVmap with selected map"""
t = metadata.tables['dgv_map']
cols = _get_cols(t)
session.execute(t.insert(),list(gen_map(cols, dgvmap)))
session.commit()
def insert_cnv_map(session, metadata, cnvmap):
"""Populate table of cnv map with a bed file"""
t = metadata.tables['cnv_map']
cols = _get_cols(t)
session.execute(t.insert(),list(gen_map(cols,cnvmap)))
session.commit()
def insert_overlap(session, metadata, overlap):
"""Populate overlap results"""
t = metadata.tables['overlap']
session.execute(t.insert(), list(overlap))
session.commit()
def insert_no_overlap(session, metadata, overlap):
"""Populate no overlap results"""
t = metadata.tables['no_overlap']
session.execute(t.insert(), list(overlap))
session.commit()
def insert_overlap_custom(session,metadata, overlap):
"""Populate overlap result from custom map"""
t = metadata.tables['overlap_custom']
session.execute(t.insert(), list(overlap))
session.commit()
def insert_gene_custom_map(session,metadata,gene_custom_map):
"""Populate a table with a custom gene map"""
t = metadata.tables['gene_custom_map']
cols = _get_cols(t)
session.execute(t.insert(),list(gen_map(cols, gene_custom_map)))
session.commit()
def insert_overlap_gene_result(session, metadata, overlap_gene_result):
""" Polupate a table with overlap_gene result"""
t = metadata.tables['overlap_gene_result']
session.execute(t.insert(),list(overlap_gene_result))
session.commit()
def empty_overlap_table(session,metadata):
t = metadata.tables['overlap']
session.execute(t.delete())
session.commit()
def empty_overlap_custom_table(session,metadata):
t = metadata.tables['overlap_custom']
session.execute(t.delete())
session.commit()
def close_and_commit(session):
"""
Commit changes to the DB and close out DB cursor.
"""
session.commit()
session.close()
def empty_tables(cursor):
cursor.execute('''delete * from variation''')
cursor.execute('''delete * from samples''')
def update_gene_summary_w_cancer_census(session, metadata, genes):
tbl = metadata.tables['gene_summary']
#http://docs.sqlalchemy.org/en/rel_1_0/core/tutorial.html?highlight=select#inserts-updates-and-deletes
stmt = tbl.update().where(sql.and_(tbl.c.gene == sql.bindparam("gene_"),
tbl.c.chrom == sql.bindparam("chrom_"))
).values(in_cosmic_census=sql.bindparam("in_cosmic_census_"))
# need the trailing underscore for bindparam
cols = ("in_cosmic_census_", "gene_", "chrom_")
session.execute(stmt, [dict(zip(cols, g)) for g in genes])
def get_session_metadata(path):
"""return an engine"""
engine = sqlalchemy.create_engine(get_path(path), isolation_level=None)
engine.connect().connection.connection.text_factory = str
engine.raw_connection().connection.text_factory = str
metadata = sql.MetaData(bind=engine)
metadata.reflect(bind=engine)
session = create_session(bind=engine, autocommit=False, autoflush=False)
session.bind.connect().connection.connection.text_factory = str
session.bind.raw_connection().connection.text_factory = str
return session, metadata
@contextlib.contextmanager
def database_transaction(db):
session, metadata = get_session_metadata(db)
conn = session.connection()
if session.bind.name == "sqlite":
conn.execute('PRAGMA synchronous = OFF')
conn.execute('PRAGMA journal_mode=MEMORY')
yield conn
session.commit()
conn.close()