def _create_sequencing_centers(self):
"""
Create sequencing center
"""
sc = {'name': random.choice(self.name_list)}
sequencing_experiments = self._create_experiments(
random.randint(self.min_seq_exps, self.max_seq_exps))
sc = SequencingCenter(**sc,
sequencing_experiments=sequencing_experiments)
db.session.add(sc)
db.session.commit()
return SequencingCenter(**sc)
def _create_save_to_db(self):
"""
Create and save sequencing_experiment
"""
sc = SequencingCenter(name='sc')
kwargs = {
'external_id': 'blah',
'experiment_strategy': 'WXS',
'library_name': 'Test_library_name_1',
'library_strand': 'Unstranded',
'is_paired_end': False,
'platform': 'Illumina',
'instrument_model': '454 GS FLX Titanium',
'max_insert_size': 600,
'mean_insert_size': 500,
'mean_depth': 40,
'total_reads': 800,
'mean_read_length': 200
}
se = SequencingExperiment(**kwargs, sequencing_center=sc)
db.session.add(se)
db.session.commit()
return se
def test_post(self):
"""
Test create a new sequencing_experiment_genomic_file
"""
# Create needed entities
gf = GenomicFile(external_id='gf0')
sc = SequencingCenter(name='sc')
se = SequencingExperiment(external_id='se0',
experiment_strategy='WGS',
is_paired_end=True,
platform='platform',
sequencing_center=sc)
db.session.add_all([gf, se])
db.session.commit()
kwargs = {'sequencing_experiment_id': se.kf_id,
'genomic_file_id': gf.kf_id,
'external_id': 'se0-gf0'
}
# Send get request
response = self.client.post(url_for(SE_GF_LIST_URL),
data=json.dumps(kwargs),
headers=self._api_headers())
# Check response status status_code
self.assertEqual(response.status_code, 201)
# Check response content
response = json.loads(response.data.decode('utf-8'))
assert response['results']['kf_id']
self.assertEqual(1, SequencingExperimentGenomicFile.query.count())
def _create_all_entities(self):
"""
Create 2 studies with genomic files and read groups
"""
sc = SequencingCenter(name='sc')
studies = []
ses = {}
gfs = {}
for j in range(2):
s = Study(external_id='s{}'.format(j))
p = Participant(external_id='p{}'.format(j))
s.participants.append(p)
study_gfs = gfs.setdefault('study{}'.format(j), [])
for i in range(3):
b = Biospecimen(external_sample_id='b{}'.format(i),
analyte_type='DNA',
sequencing_center=sc,
participant=p)
gf = GenomicFile(
external_id='study{}-gf{}'.format(j, i),
urls=['s3://mybucket/key'],
hashes={'md5': 'd418219b883fce3a085b1b7f38b01e37'})
study_gfs.append(gf)
b.genomic_files.append(gf)
study_ses = ses.setdefault('study{}'.format(j), [])
dt = datetime.now()
kwargs = {
'experiment_date': str(dt.replace(tzinfo=tz.tzutc())),
'experiment_strategy': 'WXS',
'library_name': 'Test_library_name_1',
'library_strand': 'Unstranded',
'is_paired_end': False,
'platform': 'Illumina',
'instrument_model': '454 GS FLX Titanium',
'max_insert_size': 600,
'mean_insert_size': 500,
'mean_depth': 40,
'total_reads': 800,
'mean_read_length': 200
}
se0 = SequencingExperiment(**kwargs,
sequencing_center=sc,
external_id='study{}-se0'.format(j))
se0.genomic_files.extend(study_gfs[0:2])
se1 = SequencingExperiment(**kwargs,
sequencing_center=sc,
external_id='study{}-se1'.format(j))
se1.genomic_files.extend([study_gfs[0], study_gfs[-1]])
study_ses.extend([se0, se1])
studies.append(s)
db.session.add_all(studies)
db.session.commit()
return ses, gfs, studies
def _create_save_to_db(self):
"""
Make all entities
"""
# Create sequencing_center
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
# Data
kwargs = {
'experiment_strategy': 'WXS',
'library_name': 'library',
'library_strand': 'Unstranded',
'is_paired_end': False,
'platform': 'platform',
'instrument_model': '454 GS FLX Titanium',
'max_insert_size': 600,
'mean_insert_size': 500,
'mean_depth': 40,
'total_reads': 800,
'mean_read_length': 200
}
# Create many to many se and gf
ses = []
gfs = []
for i in range(2):
gfs.append(
GenomicFile(external_id='gf{}'.format(i))
)
ses.append(
SequencingExperiment(**kwargs,
sequencing_center=sc,
external_id='se{}'.format(i))
)
db.session.add(SequencingExperimentGenomicFile(
genomic_file=gfs[0],
sequencing_experiment=ses[0],
external_id='se0-gf0'))
db.session.add(SequencingExperimentGenomicFile(
genomic_file=gfs[0],
sequencing_experiment=ses[1],
external_id='se1-gf0'))
db.session.add(SequencingExperimentGenomicFile(
genomic_file=gfs[1],
sequencing_experiment=ses[0],
external_id='se0-gf1'))
db.session.add(SequencingExperimentGenomicFile(
genomic_file=gfs[1],
sequencing_experiment=ses[1],
external_id='se1-gf1'))
db.session.commit()
return ses, gfs
def _create_entities(self):
"""
Create participant with required entities
"""
# Sequencing center
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
# Create study
study = Study(external_id='phs001')
# Participants
p = Participant(external_id='p0', is_proband=True, study=study)
# Biospecimen
bs = Biospecimen(analyte_type='dna',
sequencing_center=sc,
participant=p)
# SequencingExperiment
data = {
'external_id': 'se',
'experiment_strategy': 'wgs',
'is_paired_end': True,
'platform': 'platform',
'sequencing_center': sc
}
se = SequencingExperiment(**data)
# Genomic Files
genomic_files = []
for i in range(4):
data = {
'file_name': 'gf_{}'.format(i),
'data_type': 'submitted aligned read',
'file_format': '.cram',
'urls': ['s3://file_{}'.format(i)],
'hashes': {
'md5': str(uuid.uuid4())
},
'is_harmonized': True if i % 2 else False
}
gf = GenomicFile(**data)
bs.genomic_files.append(gf)
se.genomic_files.append(gf)
genomic_files.append(gf)
ct = self._create_cavatica_task('ct1')
db.session.add(ct)
db.session.add(study)
db.session.commit()
def test_not_null_constraint(self):
"""
Test sequencing_center can be created with out name
"""
# Create sequencing_center without name
sc = SequencingCenter(external_id='SC_0')
# Add sequencing_center to db
db.session.add(sc)
with self.assertRaises(IntegrityError):
db.session.commit()
def _create_all_entities():
"""
Create 2 studies with genomic files and read groups
"""
sc = SequencingCenter(name='sc')
studies = []
ses = {}
rgs = {}
gfs = {}
for j in range(2):
s = Study(external_id='s{}'.format(j))
p = Participant(external_id='p{}'.format(j))
s.participants.append(p)
study_gfs = gfs.setdefault('study{}'.format(j), [])
for i in range(3):
b = Biospecimen(external_sample_id='b{}'.format(i),
analyte_type='DNA',
sequencing_center=sc,
participant=p)
gf = GenomicFile(
external_id='study{}-gf{}'.format(j, i),
urls=['s3://mybucket/key', 'https://gen3.something.com/did'],
hashes={'md5': 'd418219b883fce3a085b1b7f38b01e37'})
study_gfs.append(gf)
b.genomic_files.append(gf)
study_rgs = rgs.setdefault('study{}'.format(j), [])
rg0 = ReadGroup(external_id='study{}-rg0'.format(j))
rg0.genomic_files.extend(study_gfs[0:2])
rg1 = ReadGroup(external_id='study{}-rg1'.format(j))
rg1.genomic_files.extend([study_gfs[0], study_gfs[-1]])
study_ses = ses.setdefault('study{}'.format(j), [])
se0 = SequencingExperiment(external_id='study{}-se0'.format(j),
experiment_strategy='WGS',
is_paired_end=True,
platform='platform',
sequencing_center=sc)
se0.genomic_files.extend(study_gfs[0:2])
se1 = SequencingExperiment(external_id='study{}-se1'.format(j),
experiment_strategy='WGS',
is_paired_end=True,
platform='platform',
sequencing_center=sc)
se1.genomic_files.extend([study_gfs[0], study_gfs[-1]])
study_rgs.extend([rg0, rg1])
study_ses.extend([se0, se1])
studies.append(s)
db.session.add_all(studies)
db.session.commit()
return ses, rgs, gfs, studies
def _create_save_to_db(self):
"""
Create and save sequencing_center
"""
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
kwargs = {'name': sc.name, 'kf_id': sc.kf_id}
return kwargs
def _create_biospecimens(self, total=2):
"""
Create biospecimens
"""
# Create Sequencing_center
sc = SequencingCenter(name='Baylor')
db.session.add(sc)
db.session.commit()
return [Biospecimen(external_sample_id='s{}'.format(i),
analyte_type='dna',
sequencing_center_id=sc.kf_id)
for i in range(total)]
def test_unique_constraint(self):
"""
Test name field sequencing_center can not take duplicate name
"""
ids = self.create_seqexp_seqcen()
# Create sequencing_center with same value in name
sc = SequencingCenter(external_id='SC_0', name='Baylor')
# Add sequencing_center to db
db.session.add(sc)
with self.assertRaises(IntegrityError):
db.session.commit()
def _create_save_to_db(self):
"""
Create and save diagnosis
Requires creating a participant
Create a diagnosis and add it to participant as kwarg
Save participant
"""
# Create study
study = Study(external_id='phs001')
# Create diagnosis
kwargs = {
'external_id': 'd1',
'source_text_diagnosis': 'flu',
'diagnosis_category': 'Cancer',
'source_text_tumor_location': 'Brain',
'age_at_event_days': 365,
'mondo_id_diagnosis': 'DOID:8469',
'icd_id_diagnosis': 'J10.01',
'uberon_id_tumor_location': 'UBERON:0000955',
'spatial_descriptor': 'left side'
}
d = Diagnosis(**kwargs)
# Create and save participant with diagnosis
participant_id = 'Test subject 0'
p = Participant(external_id=participant_id,
diagnoses=[d],
is_proband=True,
study=study)
db.session.add(p)
db.session.commit()
# Create sequencing center
s = SequencingCenter(name='washu')
db.session.add(s)
db.session.commit()
# Create biospecimen
b = Biospecimen(analyte_type='DNA',
sequencing_center_id=s.kf_id,
participant=p)
db.session.add(s)
db.session.add(b)
db.session.commit()
kwargs['participant_id'] = p.kf_id
kwargs['kf_id'] = d.kf_id
return kwargs
def _create_entities(self):
# Create study
study = Study(external_id='phs001')
# Create participant
p = Participant(external_id='p1',
is_proband=True, study=study)
# Create sequencing_center
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
# Create sequencing experiments
se1 = SequencingExperiment(**self._make_seq_exp('se1'),
sequencing_center_id=sc.kf_id)
se2 = SequencingExperiment(**self._make_seq_exp('se2'),
sequencing_center_id=sc.kf_id)
# Create biospecimen
bs = Biospecimen(external_sample_id='bio1', analyte_type='dna',
participant_id=p.kf_id,
sequencing_center_id=sc.kf_id)
# Create genomic files
gfs = []
for i in range(4):
kwargs = {
'file_name': 'file_{}'.format(i),
'data_type': 'submitted aligned read',
'file_format': '.cram',
'urls': ['s3://file_{}'.format(i)],
'hashes': {'md5': str(uuid.uuid4())},
'controlled_access': True,
'is_harmonized': True,
'reference_genome': 'Test01'
}
gf = GenomicFile(**kwargs,
sequencing_experiment_id=se1.kf_id)
if i % 2:
se1.genomic_files.append(gf)
else:
se2.genomic_files.append(gf)
gfs.append(gf)
bs.genomic_files = gfs
p.biospecimens = [bs]
db.session.add(p)
db.session.commit()
def _create_save_to_db(self):
"""
Create and save sequencing_experiment
"""
sc = SequencingCenter(name="Baylor")
kwargs = self._make_seq_exp(external_id='se')
se = SequencingExperiment(**kwargs,
sequencing_center_id=sc.kf_id)
sc.sequencing_experiments.extend([se])
db.session.add(sc)
db.session.commit()
kwargs['kf_id'] = se.kf_id
kwargs['sequencing_center_id'] = sc.kf_id
return kwargs
def create_seqexp(self):
"""
create sequencing_center and
sequencing experiment save the above entities to db
returns sequencing_experiment_id
"""
sc = SequencingCenter(name="Baylor")
se_id = "Test_SequencingExperiment_0"
seq_experiment_data = self._make_seq_exp(external_id=se_id)
se = SequencingExperiment(
**seq_experiment_data, sequencing_center_id=sc.kf_id)
sc.sequencing_experiments.extend([se])
db.session.add(sc)
db.session.commit()
ids = {'sequencing_experiment_id': se_id}
return ids
def _create_participants_and_dependents(self):
"""
Create participant with required entities
"""
# Create study
study = Study(external_id='phs001')
names = ['Fred', 'Wilma', 'Pebbles', 'Dino']
proband = [True, False]
participants = []
for i, _name in enumerate(names):
# Participants
p = Participant(external_id=_name,
is_proband=random.choice(proband),
study=study)
db.session.add(p)
db.session.commit()
# Sequencing center
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
# SequencingExperiment
se = self._create_experiment('se_{}'.format(i),
sequencing_center_id=sc.kf_id)
# Biospecimen
s = self._create_biospecimen('s_{}'.format(i),
sequencing_center_id=sc.kf_id,
participant_id=p.kf_id)
# Input GF
gf_in = self._create_genomic_file(
'gf_{}_in'.format(i),
sequencing_experiment_id=se.kf_id)
# Output GF
gf_out = self._create_genomic_file(
'gf_{}_out'.format(i),
data_type='aligned read',
sequencing_experiment_id=se.kf_id)
s.genomic_files = [gf_in, gf_out]
p.biospecimens = [s]
participants.append(p)
return participants
def test_post(self):
"""
Test create a new sequencing_experiment
"""
sc = SequencingCenter(name='sc')
db.session.add(sc)
db.session.commit()
kwargs = {
'external_id': 'blah',
'experiment_strategy': 'WXS',
'library_name': 'Test_library_name_1',
'library_strand': 'Unstranded',
'library_selection': 'PCR',
'library_prep': 'polyA',
'is_paired_end': False,
'platform': 'Illumina',
'instrument_model': '454 GS FLX Titanium',
'max_insert_size': 600,
'mean_insert_size': 500,
'mean_depth': 40,
'total_reads': 800,
'mean_read_length': 200,
'sequencing_center_id': sc.kf_id
}
# Send get request
response = self.client.post(url_for(SEQUENCING_EXPERIMENTS_LIST_URL),
data=json.dumps(kwargs),
headers=self._api_headers())
# Check response status status_code
self.assertEqual(response.status_code, 201)
# Check response content
response = json.loads(response.data.decode('utf-8'))
sequencing_experiment = response['results']
for k, v in kwargs.items():
if 'sequencing_center_id':
continue
self.assertEqual(sequencing_experiment[k], v)
self.assertEqual(1, SequencingExperiment.query.count())
def create_seqexp(self):
"""
create sequencing_center and
sequencing experiment save the above entities to db
returns sequencing_experiment_id
"""
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
se = SequencingExperiment(external_id="Test_seq_ex_o",
experiment_strategy="WGS",
is_paired_end="True",
platform="Test_platform",
sequencing_center_id=sc.kf_id)
sc.sequencing_experiments.extend([se])
db.session.add(sc)
db.session.commit()
ids = {
'sequencing_experiment_id': se.kf_id,
'sequencing_center_id': sc.kf_id
}
return ids
def _create_all_entities(self):
"""
Create 2 studies with genomic files and read groups
"""
sc = SequencingCenter(name='sc')
studies = []
rgs = {}
gfs = {}
for j in range(2):
s = Study(external_id='s{}'.format(j))
p = Participant(external_id='p{}'.format(j))
s.participants.append(p)
study_gfs = gfs.setdefault('study{}'.format(j), [])
for i in range(3):
b = Biospecimen(external_sample_id='b{}'.format(i),
analyte_type='DNA',
sequencing_center=sc,
participant=p)
gf = GenomicFile(
external_id='study{}-gf{}'.format(j, i),
urls=['s3://mybucket/key'],
hashes={'md5': 'd418219b883fce3a085b1b7f38b01e37'})
study_gfs.append(gf)
b.genomic_files.append(gf)
study_rgs = rgs.setdefault('study{}'.format(j), [])
rg0 = ReadGroup(external_id='study{}-rg0'.format(j))
rg0.genomic_files.extend(study_gfs[0:2])
rg1 = ReadGroup(external_id='study{}-rg1'.format(j))
rg1.genomic_files.extend([study_gfs[0], study_gfs[-1]])
study_rgs.extend([rg0, rg1])
studies.append(s)
db.session.add_all(studies)
db.session.commit()
return rgs, gfs, studies
def test_create_and_find_sequencing_experiment(self):
"""
Test creation of sequencing_exeriment
"""
dt = datetime.now()
# Create sequencing center
sc = SequencingCenter(name="Baylor")
# Create sequencing experiment
se_id = 'Test_SequencingExperiment_0'
seq_experiment_data = self._make_seq_exp(external_id=se_id)
e = SequencingExperiment(
**seq_experiment_data, sequencing_center_id=sc.kf_id)
sc.sequencing_experiments.extend([e])
db.session.add(sc)
db.session.commit()
self.assertEqual(SequencingExperiment.query.count(), 1)
se = SequencingExperiment.query.one()
for key, value in seq_experiment_data.items():
self.assertEqual(value, getattr(se, key))
self.assertGreater(se.created_at, dt)
self.assertGreater(se.modified_at, dt)
self.assertIs(type(uuid.UUID(se.uuid)), uuid.UUID)
def _create_diagnoses(self, total=2):
"""
Create diagnoses and other requred entities
"""
# Create study
study = Study(external_id='phs001')
# Create participant
participant_id = 'Test subject 0'
p = Participant(external_id=participant_id,
is_proband=True,
study=study)
# Create sequencing center
s = SequencingCenter(name='washu')
db.session.add(s)
db.session.commit()
# Create biospecimen
b = Biospecimen(analyte_type='DNA',
sequencing_center_id=s.kf_id,
participant=p)
db.session.add(p)
db.session.add(b)
db.session.commit()
# Create diagnoses
diagnoses = []
kwarg_dict = {}
for i in range(total):
d, kwargs = self._create_diagnosis(i, participant_id=p.kf_id)
kwarg_dict[d.external_id] = kwargs
diagnoses.append(d)
db.session.add_all(diagnoses)
db.session.commit()
return diagnoses, kwarg_dict
def create_seqexp_seqcen(self):
"""
create sequencial center save to db
returns sequencing_center kf_id
"""
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(external_id='SC_0', name="Baylor")
db.session.add(sc)
db.session.commit()
seq_data = {
'external_id': 'Seq_0',
'experiment_strategy': 'WXS',
'library_name': 'Test_library_name_1',
'library_strand': 'Unstranded',
'is_paired_end': False,
'platform': 'Test_platform_name_1'
}
seq_exp = SequencingExperiment(**seq_data,
sequencing_center_id=sc.kf_id)
db.session.add(seq_exp)
db.session.commit()
ids = {'sequencing_center_id': sc.kf_id}
return ids
def participants(client):
# Add a bunch of studies for pagination
for i in range(101):
s = Study(external_id='Study_{}'.format(i))
db.session.add(s)
for i in range(101):
ca = CavaticaApp(name='app', revision=0)
db.session.add(ca)
# Add a bunch of study files
s0 = Study.query.filter_by(external_id='Study_0').one()
s1 = Study.query.filter_by(external_id='Study_1').one()
for i in range(101):
sf = StudyFile(file_name='blah', study_id=s0.kf_id)
db.session.add(sf)
# Add a bunch of investigators
for _ in range(102):
inv = Investigator(name='test')
inv.studies.extend([s0, s1])
db.session.add(inv)
# Add a bunch of families
families = []
for i in range(101):
families.append(Family(external_id='Family_{}'.format(i)))
db.session.add_all(families)
db.session.flush()
participants = []
f0 = Family.query.filter_by(external_id='Family_0').one()
f1 = Family.query.filter_by(external_id='Family_1').one()
seq_cen = None
for i in range(102):
f = f0 if i < 50 else f1
s = s0 if i < 50 else s1
data = {
'external_id': "test",
'is_proband': True,
'race': 'Asian',
'ethnicity': 'Hispanic or Latino',
'diagnosis_category': 'Cancer',
'gender': 'Male'
}
p = Participant(**data, study_id=s.kf_id, family_id=f.kf_id)
diag = Diagnosis()
p.diagnoses = [diag]
outcome = Outcome()
p.outcomes = [outcome]
phen = Phenotype()
p.phenotypes = [phen]
participants.append(p)
db.session.add(p)
db.session.flush()
seq_data = {
'external_id': 'Seq_0',
'experiment_strategy': 'WXS',
'library_name': 'Test_library_name_1',
'library_strand': 'Unstranded',
'is_paired_end': False,
'platform': 'Test_platform_name_1'
}
gf_kwargs = {
'external_id': 'gf_0',
'file_name': 'hg38.fq',
'data_type': 'Aligned Reads',
'file_format': 'fastq',
'size': 1000,
'urls': ['s3://bucket/key'],
'hashes': {
'md5': str(uuid.uuid4())
},
'controlled_access': False
}
seq_cen = SequencingCenter.query.filter_by(name="Baylor")\
.one_or_none()
if seq_cen is None:
seq_cen = SequencingCenter(external_id='SC_0', name="Baylor")
db.session.add(seq_cen)
db.session.flush()
seq_exp = SequencingExperiment(**seq_data,
sequencing_center_id=seq_cen.kf_id)
db.session.add(seq_exp)
samp = Biospecimen(analyte_type='an analyte',
sequencing_center_id=seq_cen.kf_id,
participant=p)
db.session.add(samp)
p.biospecimens = [samp]
gf = GenomicFile(**gf_kwargs,
sequencing_experiment_id=seq_exp.kf_id)
db.session.add(gf)
samp.genomic_files.append(gf)
samp.diagnoses.append(diag)
db.session.flush()
rg = ReadGroup(lane_number=4, flow_cell='FL0123')
rg.genomic_files.append(gf)
ct = CavaticaTask(name='task_{}'.format(i))
ct.genomic_files.append(gf)
ca.cavatica_tasks.append(ct)
# Family relationships
for participant1, participant2 in iterate_pairwise(participants):
gender = participant1.gender
rel = 'mother'
if gender == 'male':
rel = 'father'
r = FamilyRelationship(participant1=participant1,
participant2=participant2,
participant1_to_participant2_relation=rel)
db.session.add(r)
db.session.commit()
def _create_all_entities(self):
"""
Create 2 studies with same content
Content: 3 participants, 4 biospecimens, 4 diagnoses
"""
# Create entities
sc = SequencingCenter.query.filter_by(name='sc').first()
if not sc:
sc = SequencingCenter(name='sc')
studies = []
# Two studies
for j in range(2):
s = Study(external_id='s{}'.format(j))
p0 = Participant(external_id='study{}-p0'.format(j))
p1 = Participant(external_id='study{}-p1'.format(j))
p2 = Participant(external_id='study{}-p2'.format(j))
# Participant 0
# Has 2 Biospecimens
for i in range(2):
b = Biospecimen(external_sample_id='study{}-p0-b{}'.format(
j, i),
analyte_type='DNA',
sequencing_center=sc)
# Biospecimen b0 has 2 diagnoses
if i == 0:
for k in range(2):
d = Diagnosis(
external_id='study{}-p0-d{}'.format(j, k))
p0.diagnoses.append(d)
# Biospecimen b1 has 1 diagnosis
else:
d = Diagnosis(
external_id='study{}-p0-d{}'.format(j, k + 1))
p0.diagnoses.append(d)
p0.biospecimens.append(b)
# Participant 1
# Has 1 biospecimen, 1 diagnosis
b = Biospecimen(external_sample_id='study{}-p1-b0'.format(j),
analyte_type='DNA',
sequencing_center=sc)
d = Diagnosis(external_id='study{}-p1-d0'.format(j))
p1.biospecimens.append(b)
p1.diagnoses.append(d)
# Participant 2
# Has 1 biospecimen
b = Biospecimen(external_sample_id='study{}-p2-b0'.format(j),
analyte_type='DNA',
sequencing_center=sc)
p2.biospecimens.append(b)
s.participants.extend([p0, p1, p2])
studies.append(s)
db.session.add_all(studies)
db.session.commit()
# Create links between bios and diags
bs_dgs = []
# Participant 0
p0 = studies[0].participants[0]
# b0-d0
bs_dgs.append(
BiospecimenDiagnosis(biospecimen_id=p0.biospecimens[0].kf_id,
diagnosis_id=p0.diagnoses[0].kf_id))
# b0-d1
bs_dgs.append(
BiospecimenDiagnosis(biospecimen_id=p0.biospecimens[0].kf_id,
diagnosis_id=p0.diagnoses[1].kf_id))
# b1-d2
bs_dgs.append(
BiospecimenDiagnosis(biospecimen_id=p0.biospecimens[1].kf_id,
diagnosis_id=p0.diagnoses[2].kf_id))
# b0-d2
bs_dgs.append(
BiospecimenDiagnosis(biospecimen_id=p0.biospecimens[0].kf_id,
diagnosis_id=p0.diagnoses[2].kf_id))
# Participant 1
p1 = studies[0].participants[1]
# b0-d0
bs_dgs.append(
BiospecimenDiagnosis(biospecimen_id=p1.biospecimens[0].kf_id,
diagnosis_id=p1.diagnoses[0].kf_id))
db.session.add_all(bs_dgs)
db.session.commit()
def _create_save_to_db(self):
"""
Create and save biospecimen
Requires creating a participant
Create a biospecimen and add it to participant as kwarg
Save participant
"""
dt = datetime.now()
study = Study(external_id='phs001')
db.session.add(study)
db.session.commit()
sc = SequencingCenter.query.filter_by(name="Baylor").one_or_none()
if sc is None:
sc = SequencingCenter(name="Baylor")
db.session.add(sc)
db.session.commit()
se = SequencingExperiment(external_id="Test_seq_ex_o",
experiment_strategy="WGS",
is_paired_end="True",
platform="Test_platform",
sequencing_center_id=sc.kf_id)
db.session.add(se)
db.session.commit()
# Create biospecimen
kwargs = {
'external_sample_id': 's1',
'external_aliquot_id': 'a1',
'source_text_tissue_type': 'Normal',
'composition': 'composition1',
'source_text_anatomical_site': 'Brain',
'age_at_event_days': 365,
'source_text_tumor_descriptor': 'Metastatic',
'shipment_origin': 'CORIELL',
'analyte_type': 'DNA',
'concentration_mg_per_ml': 100,
'volume_ul': 12.67,
'shipment_date': dt,
'spatial_descriptor': 'left side',
'ncit_id_tissue_type': 'Test',
'ncit_id_anatomical_site': 'C12439',
'uberon_id_anatomical_site': 'UBERON:0000955',
'consent_type': 'GRU-IRB',
'dbgap_consent_code': 'phs00000.c1',
'sequencing_center_id': sc.kf_id
}
d = Biospecimen(**kwargs)
# Create and save participant with biospecimen
p = Participant(external_id='Test subject 0',
biospecimens=[d],
is_proband=True,
study_id=study.kf_id)
db.session.add(p)
db.session.commit()
kwargs['participant_id'] = p.kf_id
kwargs['kf_id'] = d.kf_id
return kwargs