def get_single_dna_extract_json(cache, study, study_md, subj_var_values,
samp_var_values):
# Almost all samples in TOPMed WGS phase are blood samples, named "Blood", "Peripheral Blood"...
# Few samples are saliva samples probably due to sample collection issues
name = None
if 'BODY_SITE' in samp_var_values:
name = 'BODY_SITE'
elif 'Body_Site' in samp_var_values:
name = 'Body_Site'
elif 'Body Site' in samp_var_values:
name = 'Body Site'
anat_id = None
anatomy_name = None
if name is not None:
if "blood" in samp_var_values[name]['value'].lower():
anatomy_name = "blood"
anat_id = "0000178"
elif samp_var_values[name]['value'].lower() == "saliva":
anatomy_name = "saliva"
anat_id = "0001836"
else:
logging.fatal(
"encountered BODY_SITE other than 'Blood' and 'Saliva' in TOPMed sample metadata - "
+ samp_var_values['BODY_SITE']['value'])
sys.exit(1)
if anat_id is not None:
anatomy_identifier = OrderedDict([("identifier",
"UBERON:" + str(anat_id)),
("identifierSource", "UBERON")])
anatomy_alt_ids = [
OrderedDict([
("identifier",
"http://purl.obolibrary.org/obo/UBERON_" + str(anat_id)),
("identifierSource", "UBERON")
])
]
# extract subject attributes
gender = None
age = None
visit_year = None
sys_bp = None
dias_bp = None
disease = {}
disease['hypertension'] = "unknown"
for name in subj_var_values:
name_upper = name.upper()
if name_upper == "GENDER" or name_upper == "SEX":
gender = subj_var_values[name]['value'].lower()
elif name_upper == "VISIT_AGE" or name_upper == "AGE" or name_upper == "AGE_ENROLL": #need to confirm that these allmean the same thing
age = subj_var_values[name]['value']
elif name_upper == "VISIT_YEAR":
visit_year = subj_var_values[name]['value']
elif name_upper == "SYSBP":
sys_bp = subj_var_values[name]['value']
elif name_upper == "DIASBP":
dias_bp = subj_var_values[name]['value']
elif name_upper == "HYPERTENSION" or name_upper == "HIGHBLOODPRES":
if subj_var_values[name]['value'].lower(
) == "yes" or subj_var_values[name]['value'] == '1':
disease['hypertension'] = "yes"
elif re.match(r'\S', subj_var_values[name]['value']):
disease['hypertension'] = "no"
# anatomical part
anatomical_part = None
if anatomy_name is not None:
anatomical_part = DatsObj("AnatomicalPart",
[("name", anatomy_name),
("identifier", anatomy_identifier),
("alternateIdentifiers", anatomy_alt_ids)])
subject_characteristics = []
subject_bearerOfDisease = []
# harmonized/standardized characteristics
if gender is not None:
subject_sex = DatsObj(
"Dimension",
[("name", DatsObj("Annotation", [("value", "Gender")])),
("description", "Gender of the subject"), ("values", [gender])])
subject_characteristics.append(subject_sex)
if age is not None:
subject_age = DatsObj(
"Dimension", [("name", DatsObj("Annotation", [("value", "Age")])),
("description", "Age of the subject"),
("values", [age])])
subject_characteristics.append(subject_age)
if visit_year is not None:
subject_visitYear = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Visit year")])),
("description", "Year of visit, to use for longitudinal analysis"),
("values", [visit_year])
])
subject_characteristics.append(subject_visitYear)
if sys_bp is not None:
subject_sysBP = DatsObj(
"Dimension",
[("name",
DatsObj("Annotation", [("value", "Systolic blood pressure")])),
("description",
"Systolic blood pressure of subject, measured in mmHg"),
("values", [sys_bp])])
subject_characteristics.append(subject_sysBP)
if dias_bp is not None:
subject_diasBP = DatsObj(
"Dimension",
[("name",
DatsObj("Annotation", [("value", "Diastolic blood pressure")])),
("description",
"Diastolic blood pressure of subject, measured in mmHg"),
("values", [dias_bp])])
subject_characteristics.append(subject_diasBP)
if disease['hypertension'] != "unknown":
disease_name = "hypertension"
disease_id = "10763"
disease_identifier = OrderedDict([
("identifier", "DOID:" + str(disease_id)),
("identifierSource", "Disease Ontology")
])
disease_alt_ids = [
OrderedDict([
("identifier",
"http://purl.obolibrary.org/obo/DOID_" + str(disease_id)),
("identifierSource", "Disease Ontology")
])
]
subject_hypertension = DatsObj("Disease", [
("name", "Hypertension"),
("identifier", disease_identifier),
("alternateIdentifiers", disease_alt_ids),
("diseaseStatus",
DatsObj("Annotation", [("value", disease['hypertension']),
("valueIRI", "")])),
])
subject_bearerOfDisease.append(subject_hypertension)
# create a DATS Dimension from a dbGaP variable value
def make_var_dimension(name, var_value):
value = var_value["value"]
dim = DatsObj("Dimension",
[("name", DatsObj("Annotation", [("value", name)])),
("values", [value])])
# find existing DATS identifier for the corresponding Dataset Dimension
if "var" in var_value:
id = var_value["var"]["id"]
dbgap_var_dim = study_md['dbgap_vars'][id]
dim.setProperty("identifier",
dbgap_var_dim.get("identifier").getIdRef())
return dim
# create DATS Dimensions for dbGaP subject metadata
subject_dimensions = [
make_var_dimension(vname, subj_var_values[vname])
for vname in sorted(subj_var_values)
]
# create DATS Dimensions for dbGaP sample metadata
sample_dimensions = [
make_var_dimension(vname, samp_var_values[vname])
for vname in sorted(samp_var_values)
]
# "raw" characteristics from dbGaP metadata
subject_characteristics.extend(subject_dimensions)
sample_characteristics = sample_dimensions
human_t = util.get_taxon_human(cache)
subj_id = subj_var_values['SUBJECT_ID']['value']
dbgap_subj_id = subj_var_values['dbGaP_Subject_ID']['value']
samp_id = samp_var_values['SAMPLE_ID']['value']
dbgap_samp_id = samp_var_values['dbGaP_Sample_ID']['value']
study_title = study.get("title")
# human experimental subject/patient
subject_material = DatsObj(
"Material",
[("name", subj_id), ("identifier", {
"identifier": subj_id
}),
("alternateIdentifiers", [util.get_alt_id(dbgap_subj_id, "dbGaP")]),
("description", study_title + " subject " + subj_id),
("characteristics", subject_characteristics),
("bearerOfDisease", subject_bearerOfDisease), ("taxonomy", [human_t]),
("roles", util.get_donor_roles(cache))])
# TODO - use DatsObjCache
specimen_annot = util.get_annotation("specimen")
dna_extract_annot = util.get_annotation("DNA extract")
# biological/tissue sample
sample_name = samp_id
sample_derives_from = [subject_material]
sample_descr = "specimen collected from subject " + subj_id
if anatomical_part is not None:
sample_derives_from.append(anatomical_part)
sample_descr = anatomy_name + " " + sample_descr
biological_sample_material = DatsObj(
"Material",
[("name", sample_name), ("identifier", {
"identifier": samp_id
}),
("alternateIdentifiers", [util.get_alt_id(dbgap_samp_id, "dbGaP")]),
("description", sample_descr),
("characteristics", sample_characteristics), ("taxonomy", [human_t]),
("roles", [specimen_annot]), ("derivesFrom", sample_derives_from)])
# DNA extracted from tissue sample
dna_descr = "DNA extracted from specimen collected from subject " + subj_id
if anatomical_part is not None:
dna_descr = "DNA extracted from " + anatomy_name + " specimen collected from subject " + subj_id
dna_material = DatsObj("Material",
[("name", "DNA from " + sample_name),
("description", dna_descr),
("taxonomy", [human_t]),
("roles", [dna_extract_annot]),
("derivesFrom", [biological_sample_material])])
return dna_material
def get_sample_dats_material(cache, dats_subject, study, study_md,
samp_var_values):
# Almost all samples in TOPMed WGS phase are blood samples, named "Blood", "Peripheral Blood"...
# Few samples are saliva samples probably due to sample collection issues
name = None
if 'BODY_SITE' in samp_var_values:
name = 'BODY_SITE'
elif 'Body_Site' in samp_var_values:
name = 'Body_Site'
elif 'Body Site' in samp_var_values:
name = 'Body Site'
anat_id = None
anatomy_name = None
if name is not None:
if "blood" in samp_var_values[name]['value'].lower():
anatomy_name = "blood"
anat_id = "0000178"
elif samp_var_values[name]['value'].lower() == "saliva":
anatomy_name = "saliva"
anat_id = "0001836"
else:
logging.fatal(
"encountered BODY_SITE other than 'Blood' and 'Saliva' in TOPMed sample metadata - "
+ samp_var_values['BODY_SITE']['value'])
sys.exit(1)
def make_anat_part(anat_id, anatomy_name):
# anatomical part
anatomical_part = DatsObj("AnatomicalPart", [("name", anatomy_name)])
if anat_id is not None:
anatomy_identifier = OrderedDict([("identifier",
"UBERON:" + str(anat_id)),
("identifierSource", "UBERON")])
anatomy_alt_ids = [
OrderedDict([
("identifier",
"http://purl.obolibrary.org/obo/UBERON_" + str(anat_id)),
("identifierSource", "UBERON")
])
]
anatomical_part.set("identifier", anatomy_identifier)
anatomical_part.set("alternateIdentifiers", anatomy_alt_ids)
return anatomical_part
if anatomy_name is not None:
# use cached value for AnatomicalPart if possible
anat_part_key = ":".join(["AnatomicalPart", anatomy_name])
anatomical_part = cache.get_obj_or_ref(
anat_part_key, lambda: make_anat_part(anat_id, anatomy_name))
else:
anatomical_part = None
# create a DATS Dimension from a dbGaP variable value
def make_var_dimension(name, var_value):
value = var_value["value"]
dim = DatsObj("Dimension",
[("name", DatsObj("Annotation", [("value", name)])),
("values", [value])])
# find existing DATS identifier for the corresponding Dataset Dimension
if "var" in var_value:
dbgap_var_dim = var_value["var"]["dim"]
dim.setProperty("identifier",
dbgap_var_dim.get("identifier").getIdRef())
return dim
# create DATS Dimensions for dbGaP sample metadata
sample_dimensions = [
make_var_dimension(vname, samp_var_values[vname])
for vname in sorted(samp_var_values)
]
sample_characteristics = sample_dimensions
samp_id = samp_var_values['SAMPLE_ID']['value']
dbgap_samp_id = samp_var_values['dbGaP_Sample_ID']['value']
study_title = study.get("title")
specimen_annot = util.get_annotation("specimen", cache)
# corresponding DATS subject Material
subj_key = ":".join(["Material", dats_subject.get("name")])
dats_subj = cache.get_obj_or_ref(subj_key, lambda: dats_subject)
dats_subj_name = dats_subject.get("name")
# biological/tissue sample
sample_name = samp_id
sample_derives_from = [dats_subj]
sample_descr = "specimen collected from subject " + dats_subj_name
if anatomical_part is not None:
sample_derives_from.append(anatomical_part)
sample_descr = anatomy_name + " " + sample_descr
biological_sample_material = DatsObj(
"Material",
[("name", sample_name), ("identifier", {
"identifier": samp_id
}),
("alternateIdentifiers", [util.get_alt_id(dbgap_samp_id, "dbGaP")]),
("description", sample_descr),
("characteristics", sample_characteristics),
("taxonomy", [util.get_taxon_human(cache)]),
("roles", [specimen_annot]), ("derivesFrom", sample_derives_from)])
# RNA or DNA extracted from tissue sample
stype = "DNA"
# TODO - check if RNA, not DNA
dna_or_rna_descr = stype + " extracted from specimen collected from subject " + dats_subj_name
if anatomical_part is not None:
dna_or_rna_descr = stype + " extracted from " + anatomy_name + " specimen collected from subject " + dats_subj_name
dna_or_rna_material = DatsObj(
"Material",
[("name", stype + " from " + sample_name),
("description", dna_or_rna_descr),
("taxonomy", [util.get_taxon_human(cache)]),
("roles", [util.get_annotation(stype + " extract", cache)]),
("derivesFrom", [biological_sample_material])])
return dna_or_rna_material
def get_subject_dats_material(cache, study, study_md, subj_var_values):
# extract subject attributes
gender = None
age = None
visit_year = None
sys_bp = None
dias_bp = None
disease = {}
disease['hypertension'] = "unknown"
for name in subj_var_values:
name_upper = name.upper()
if name_upper == "GENDER" or name_upper == "SEX":
gender = subj_var_values[name]['value'].lower()
elif name_upper == "VISIT_AGE" or name_upper == "AGE" or name_upper == "AGE_ENROLL": #need to confirm that these allmean the same thing
age = subj_var_values[name]['value']
elif name_upper == "VISIT_YEAR":
visit_year = subj_var_values[name]['value']
elif name_upper == "SYSBP":
sys_bp = subj_var_values[name]['value']
elif name_upper == "DIASBP":
dias_bp = subj_var_values[name]['value']
elif name_upper == "HYPERTENSION" or name_upper == "HIGHBLOODPRES":
if subj_var_values[name]['value'].lower() == "yes" or subj_var_values[name]['value'] == '1':
disease['hypertension'] = "yes"
elif re.match(r'\S', subj_var_values[name]['value']):
disease['hypertension'] = "no"
subject_characteristics = []
subject_bearerOfDisease = []
# harmonized/standardized characteristics
if gender is not None:
subject_sex = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Gender")])),
("description", "Gender of the subject"),
("values", [ gender ])
])
subject_characteristics.append(subject_sex)
if age is not None:
subject_age = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Age")])),
("description", "Age of the subject"),
("values", [ age ])
])
subject_characteristics.append(subject_age)
if visit_year is not None:
subject_visitYear = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Visit year")])),
("description", "Year of visit, to use for longitudinal analysis"),
("values", [ visit_year ])
])
subject_characteristics.append(subject_visitYear)
if sys_bp is not None:
subject_sysBP = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Systolic blood pressure")])),
("description", "Systolic blood pressure of subject, measured in mmHg"),
("values", [ sys_bp ])
])
subject_characteristics.append(subject_sysBP)
if dias_bp is not None:
subject_diasBP = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Diastolic blood pressure")])),
("description", "Diastolic blood pressure of subject, measured in mmHg"),
("values", [ dias_bp ])
])
subject_characteristics.append(subject_diasBP)
if disease['hypertension'] != "unknown":
disease_name = "hypertension"
disease_id = "10763"
disease_identifier = OrderedDict([
("identifier", "DOID:" + str(disease_id)),
("identifierSource", "Disease Ontology")])
disease_alt_ids = [OrderedDict([
("identifier", "http://purl.obolibrary.org/obo/DOID_" + str(disease_id)),
("identifierSource", "Disease Ontology")])]
subject_hypertension = DatsObj("Disease", [
("name", "Hypertension"),
("identifier", disease_identifier),
("alternateIdentifiers", disease_alt_ids),
("diseaseStatus", DatsObj("Annotation", [("value", disease['hypertension'] ), ("valueIRI", "")])),
])
subject_bearerOfDisease.append(subject_hypertension)
# create a DATS Dimension from a dbGaP variable value
def make_var_dimension(name, var_value):
value = var_value["value"]
dim = DatsObj("Dimension",
[("name", DatsObj("Annotation", [( "value", name )])),
("values", [ value ])
])
# find existing DATS identifier for the corresponding Dataset Dimension
if "var" in var_value:
dbgap_var_dim = var_value["var"]["dim"]
dim.setProperty("identifier", dbgap_var_dim.get("identifier").getIdRef())
return dim
# create DATS Dimensions for dbGaP subject metadata
subject_dimensions = [ make_var_dimension(vname, subj_var_values[vname]) for vname in sorted(subj_var_values) ]
# "raw" characteristics from dbGaP metadata
subject_characteristics.extend(subject_dimensions)
human_t = util.get_taxon_human(cache)
subj_id = subj_var_values['SUBJECT_ID']['value']
dbgap_subj_id = subj_var_values['dbGaP_Subject_ID']['value']
study_title = study.get("title")
# human experimental subject/patient
subject_material = DatsObj("Material", [
("name", subj_id),
("identifier", { "identifier": subj_id }),
("alternateIdentifiers", [ util.get_alt_id(dbgap_subj_id, "dbGaP") ]),
("description", study_title + " subject " + subj_id),
("characteristics", subject_characteristics),
("bearerOfDisease", subject_bearerOfDisease),
("taxonomy", [ human_t ]),
("roles", util.get_donor_roles(cache))
])
# add to the cache
subj_key = ":".join(["Material", subj_id])
dats_subj = cache.get_obj_or_ref(subj_key, lambda: subject_material)
return dats_subj
def get_single_dna_extract_json(study, subj_var_values, samp_var_values):
# all samples in TOPMed WGS phase are blood samples
if samp_var_values['BODY_SITE'] != 'Blood':
logging.fatal(
"encountered BODY_SITE other than 'Blood' in TOPMed sample metadata - "
+ samp_var_values['BODY_SITE'])
sys.exit(1)
anatomy_name = "blood"
anat_id = "0000178"
anatomy_identifier = OrderedDict([("identifier", "UBERON:" + str(anat_id)),
("identifierSource", "UBERON")])
anatomy_alt_ids = [
OrderedDict([("identifier",
"http://purl.obolibrary.org/obo/UBERON_" + str(anat_id)),
("identifierSource", "UBERON")])
]
# extract subject attributes
gender = None
age = None
for name in subj_var_values:
if name == "GENDER":
gender = subj_var_values[name].lower()
elif name == "VISIT_AGE":
age = subj_var_values[name]
# TODO - determine what other subject attributes can be mapped directly to core DATS objects
# place original dbGaP subject metadata into extraProperties
# TODO - consider alternative of doing this only for un-harmonized metadata
subj_extra_props = [
DatsObj("CategoryValuesPair", [("category", xp),
("values", [subj_var_values[xp]])])
for xp in sorted(subj_var_values)
]
# extract sample attributes
for name in samp_var_values:
if name == 'SEQUENCING_CENTER':
# TODO - determine which DATS objects (e.g., biological sample, DNA prep, sequence data) this property should attach to
pass
# TODO - determine what other subject attributes can be mapped directly to core DATS objects
# e.g., IS_TUMOR -> bearerOfDisease ("the pathology affecting the material...")
# place original dbGaP sample metadata into extraProperties
samp_extra_props = [
DatsObj("CategoryValuesPair", [("category", xp),
("values", [samp_var_values[xp]])])
for xp in sorted(samp_var_values)
]
# anatomical part
anatomical_part = DatsObj("AnatomicalPart",
[("name", anatomy_name),
("identifier", anatomy_identifier),
("alternateIdentifiers", anatomy_alt_ids)])
subject_sex = DatsObj("Dimension", [("name", {
"value": "Gender"
}), ("description", "Gender of the subject"), ("values", [gender])])
subject_age = DatsObj("Dimension", [("name", {
"value": "Age"
}), ("description", "Age of the subject"), ("values", [age])])
subject_characteristics = [subject_sex, subject_age]
human_t = util.get_taxon_human()
subj_id = subj_var_values['SUBJECT_ID']
dbgap_subj_id = subj_var_values['dbGaP_Subject_ID']
samp_id = samp_var_values['SAMPLE_ID']
dbgap_samp_id = samp_var_values['dbGaP_Sample_ID']
study_title = study.get("title")
# human experimental subject/patient
subject_material = DatsObj(
"Material",
[("name", subj_id), ("identifier", {
"identifier": subj_id
}),
("alternateIdentifiers", [util.get_alt_id(dbgap_subj_id, "dbGaP")]),
("description", study_title + " subject " + subj_id),
("characteristics", subject_characteristics), ("taxonomy", human_t),
("roles", util.get_donor_roles()),
("extraProperties", subj_extra_props)])
# biological/tissue sample
sample_name = samp_id
biological_sample_material = DatsObj(
"Material",
[("name", sample_name), ("identifier", {
"identifier": samp_id
}),
("alternateIdentifiers", [util.get_alt_id(dbgap_samp_id, "dbGaP")]),
("description",
anatomy_name + " specimen collected from subject " + subj_id),
("taxonomy", human_t),
("roles", [OrderedDict([("value", "specimen"), ("valueIRI", "")])]),
("derivesFrom", [subject_material, anatomical_part]),
("extraProperties", samp_extra_props)])
# DNA extracted from tissue sample
dna_material = DatsObj(
"Material",
[("name", "DNA from " + sample_name),
("description", "DNA extracted from " +
anatomy_name + " specimen collected from subject " + subj_id),
("taxonomy", human_t),
("roles", [OrderedDict([("value", "DNA extract"),
("valueIRI", "")])]),
("derivesFrom", [biological_sample_material])])
return dna_material
def update_single_subject(cache, study, study_md, subj, subj_var_values,
use_all_dbgap_vars):
# extract subject attributes
gender = None
age = None
visit_year = None
sys_bp = None
dias_bp = None
disease = {}
disease['hypertension'] = "unknown"
for name in subj_var_values:
name_upper = name.upper()
if name_upper == "GENDER" or name_upper == "SEX":
gender = subj_var_values[name]['value'].lower()
elif name_upper == "VISIT_AGE" or name_upper == "AGE" or name_upper == "AGE_ENROLL": #need to confirm that these allmean the same thing
age = subj_var_values[name]['value']
elif name_upper == "VISIT_YEAR":
visit_year = subj_var_values[name]['value']
elif name_upper == "SYSBP":
sys_bp = subj_var_values[name]['value']
elif name_upper == "DIASBP":
dias_bp = subj_var_values[name]['value']
elif name_upper == "HYPERTENSION" or name_upper == "MHHTN":
if subj_var_values[name]['value'].lower(
) == "yes" or subj_var_values[name]['value'] == '1':
disease['hypertension'] = "yes"
elif re.match(r'\S', subj_var_values[name]['value']):
disease['hypertension'] = "no"
subject_characteristics = []
subject_bearerOfDisease = []
# harmonized/standardized characteristics
if gender is not None:
# TODO - this
ss = None
if gender == "2":
ss = "female"
if gender == "1":
ss = "male"
subject_sex = DatsObj(
"Dimension",
[("name", DatsObj("Annotation", [("value", "Gender")])),
("description", "Gender of the subject"), ("values", [ss])])
subject_characteristics.append(subject_sex)
if age is not None:
subject_age = DatsObj(
"Dimension", [("name", DatsObj("Annotation", [("value", "Age")])),
("description", "Age of the subject"),
("values", [age])])
subject_characteristics.append(subject_age)
if visit_year is not None:
subject_visitYear = DatsObj("Dimension", [
("name", DatsObj("Annotation", [("value", "Visit year")])),
("description", "Year of visit, to use for longitudinal analysis"),
("values", [visit_year])
])
subject_characteristics.append(subject_visitYear)
if sys_bp is not None:
subject_sysBP = DatsObj(
"Dimension",
[("name",
DatsObj("Annotation", [("value", "Systolic blood pressure")])),
("description",
"Systolic blood pressure of subject, measured in mmHg"),
("values", [sys_bp])])
subject_characteristics.append(subject_sysBP)
if dias_bp is not None:
subject_diasBP = DatsObj(
"Dimension",
[("name",
DatsObj("Annotation", [("value", "Diastolic blood pressure")])),
("description",
"Diastolic blood pressure of subject, measured in mmHg"),
("values", [dias_bp])])
subject_characteristics.append(subject_diasBP)
if disease['hypertension'] != "unknown":
disease_name = "hypertension"
disease_id = "10763"
disease_identifier = OrderedDict([
("identifier", "DOID:" + str(disease_id)),
("identifierSource", "Disease Ontology")
])
disease_alt_ids = [
OrderedDict([
("identifier",
"http://purl.obolibrary.org/obo/DOID_" + str(disease_id)),
("identifierSource", "Disease Ontology")
])
]
subject_hypertension = DatsObj(
"Disease",
[("name", "Hypertension"), ("identifier", disease_identifier),
("alternateIdentifiers", disease_alt_ids),
("diseaseStatus",
DatsObj("Annotation", [("value", disease['hypertension'])]))])
subject_bearerOfDisease.append(subject_hypertension)
# create a DATS Dimension from a dbGaP variable value
def make_var_dimension(name, var_value):
value = var_value["value"]
dim = DatsObj("Dimension",
[("name", DatsObj("Annotation", [("value", name)])),
("values", [value])])
# find existing DATS identifier for the corresponding Dataset Dimension
if "var" in var_value:
dim.setProperty(
"identifier",
var_value["var"]["dim"].get("identifier").getIdRef())
return dim
# add "raw" characteristics / DATS Dimensions for _all_ dbGaP subject metadata
# create DATS Dimensions for dbGaP subject metadata
if use_all_dbgap_vars:
subject_dimensions = [
make_var_dimension(vname, subj_var_values[vname])
for vname in sorted(subj_var_values)
]
subject_characteristics.extend(subject_dimensions)
# update subject
dbgap_subj_id = subj_var_values['dbGaP_Subject_ID']['value']
subj.set("alternateIdentifiers", [util.get_alt_id(dbgap_subj_id, "dbGaP")])
subj.set("bearerOfDisease", subject_bearerOfDisease)
# update characteristics
chars = subj.get("characteristics")
new_chars = []
# remove values from public data release that will be overwritten
for c in chars:
name = c.get("name")
# TODO - 'member of study group' is string, not Annotation
if not isinstance(name, DatsObj) and name == 'member of study group':
new_chars.append(c)
new_chars.extend(subject_characteristics)
subj.set("characteristics", new_chars)
def get_gene_json(cache, mod, gff3_json_path, orthologs):
# read gene features form BGI file
features = read_bgi(cache, mod, gff3_json_path)
# read disease info from disease JSON file
diseases = read_disease(cache, mod, gff3_json_path)
# read disease info from disease JSON file
phenotypes = read_phenotype(cache, mod, gff3_json_path)
# TODO - read gene features from GFF3 file
genes = []
for f in features:
genomeLocations = DatsObj("GenomeLocation",
[("assembly", f['assembly']),
("chromosome", f['chr']),
("startPosition", f['start']),
("endPosition", f['end']),
("strand", f['strand'])])
roles = [
DatsObj("Annotation",
[("value", SOID[f['soid']]),
("valueIRI",
"http://purl.obolibrary.org/obo/SO_" + f['soid'][3:])])
]
alternate_ids = []
if f['alt_ids'] != "NA":
alt_ids_list = []
for i in f['alt_ids']:
source, id = i.split(':')
alt_id = util.get_alt_id(id, source)
alternate_ids.append(alt_id)
#encode disease
disease_list = []
gene_diseases = search_dict('object_id', f['primaryId'], diseases)
if len(gene_diseases) > 0:
do_ids = [d['do_id'] for d in gene_diseases]
uniq_do_ids = list(set(do_ids))
for d in uniq_do_ids:
disease_id = DatsObj(
"Annotation",
[("value", d),
("valueIRI",
"http://purl.obolibrary.org/obo/DOID_" + d[5:])])
select_diseases = search_dict('do_id', d, gene_diseases)
#relation = OrderedDict([("value", select_diseases[0]['association_type'])])
relation = DatsObj(
"Annotation",
[("value", "Disease"),
("valueIRI", "http://purl.obolibrary.org/obo/DOID_4")])
# account for multiple evidence codes per disease id
evd_ids = []
evd_ids_list = [d['evidence_codes'] for d in select_diseases]
for i in evd_ids_list[0]:
evd_id = DatsObj(
"Annotation",
[("value", i),
("valueIRI",
"http://purl.obolibrary.org/obo/" + EVID[i])])
evd_ids.append(evd_id)
# account for multiple publications per disease id
pub_ids = []
pub_ids_list = [d['pubmed_id'] for d in select_diseases]
for i in pub_ids_list:
pub_id = DatsObj(
"Publication",
[("Identifier",
DatsObj("Identifier",
[("identifier", i),
("identifierSource", "PubMed")]))])
pub_ids.append(pub_id)
mod_pub_ids_list = [d['mod_pub_id'] for d in select_diseases]
for i in mod_pub_ids_list:
mod_pub_id = DatsObj("Publication", [
("Identifier",
DatsObj("Identifier", [("identifier", i),
("identifierSource", i[:3])]))
])
pub_ids.append(mod_pub_id)
relation_evidence = OrderedDict([
("evidenceCodes", evd_ids), ("publications", pub_ids),
("dateEstablished",
DatsObj("Date", [
("date", select_diseases[0]['date_ass']),
("type",
DatsObj("Annotation", [("value", "Date Assigned")]))
]))
])
related_entity_id = OrderedDict([
("object", disease_id), ("relation", relation),
("resultingFrom",
DatsObj(
"Activity",
[("name", select_diseases[0]['association_type'])])),
("relationEvidence", relation_evidence)
])
disease_list.append(related_entity_id)
#encode phenotype
#assumes one phenotype termID per record as is in RGD and MGI phenotype JSONs
phenotype_list = []
gene_phenotypes = search_dict('object_id', f['primaryId'], phenotypes)
if len(gene_phenotypes) > 0:
phe_ids = [p['phe_term_ids'] for p in gene_phenotypes]
#logging.info("phe_ids: " + str(phe_ids))
uniq_phe_ids = list(set(phe_ids))
for p in uniq_phe_ids:
select_phenotypes = search_dict('phe_term_ids', p,
gene_phenotypes)
#logging.info("select_phe: " + str(select_phenotypes))
term_id = DatsObj(
"Annotation",
[("value", select_phenotypes[0]['phe_term_ids']),
("valueIRI", "http://purl.obolibrary.org/obo/MP_" +
select_phenotypes[0]['phe_term_ids'][3:])])
relation = DatsObj("Annotation", [
("value", "Phenotype"),
("valueIRI", "http://purl.obolibrary.org/obo/OGMS_0000023")
])
# account for multiple publications per phenotype
pub_ids = []
empt = ''
pub_ids_list = [p['pubmed_id'] for p in select_phenotypes]
for i in pub_ids_list:
if i == "":
continue
else:
pub_id = DatsObj(
"Publication",
[("Identifier",
DatsObj("Identifier",
[("identifier", i),
("identifierSource", "PubMed")]))])
pub_ids.append(pub_id)
mod_pub_ids_list = [p['mod_pub_id'] for p in select_phenotypes]
for i in mod_pub_ids_list:
mod_pub_id = DatsObj("Publication", [
("Identifier",
DatsObj("Identifier", [("identifier", i),
("identifierSource", i[:3])]))
])
pub_ids.append(mod_pub_id)
relation_evidence = OrderedDict([
("publications", pub_ids),
("dateEstablished",
DatsObj("Date", [
("date", select_phenotypes[0]['date_ass']),
("type",
DatsObj("Annotation", [("value", "Date Assigned")]))
]))
])
related_entity_id = OrderedDict([("object", term_id),
("relation", relation),
("relationEvidence",
relation_evidence)])
phenotype_list.append(related_entity_id)
#encode ortholog
ortholog_list = []
gene_orthologs = search_dict('mod_gene_id', f['primaryId'], orthologs)
if len(gene_orthologs) > 0:
for o in gene_orthologs:
if '9606' in o['ortho_taxon']:
o_taxon = util.get_taxon_human(cache)
else:
logging.fatal("encountered taxonomy other human - " +
o['ortho_taxon'])
sys.exit(1)
mol_entity_ortholog = DatsObj("MolecularEntity", [
("identifier",
DatsObj("Identifier",
[("identifier", o['ortho_gene_id'])])),
("name", o['ortho_gene_id']),
("taxonomy", [o_taxon]),
("alternateIdentifiers",
util.get_alt_id(o['ortho_gene_symbol'], "Gene Symbol")),
])
related_entity_id = OrderedDict([
("object", mol_entity_ortholog),
("relation",
DatsObj("Annotation",
[("value", "Orthology"),
("valueIRI",
"http://purl.obolibrary.org/obo/HOM_0000017")]))
])
ortholog_list.append(related_entity_id)
related_entities = disease_list + phenotype_list + ortholog_list
gene = DatsObj(
"MolecularEntity",
[("identifier",
DatsObj("Identifier", [("identifier", f['primaryId'])])),
("name", f['primaryId']), ("description", f['descr']),
("roles", roles), ("taxonomy", [f['taxon']]),
("genomeLocations", [genomeLocations]),
("alternateIdentifiers", alternate_ids),
("relatedEntities", related_entities)])
genes.append(gene)
return genes