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"""Tests for VariantCalling CLIF python wrappers."""
from absl.testing import absltest
from deepvariant import testdata
from deepvariant.protos import deepvariant_pb2
from deepvariant.python import allelecounter as _allelecounter
from deepvariant.python import variant_calling_multisample
from third_party.nucleus.io import fasta
from third_party.nucleus.io import sam
from third_party.nucleus.util import ranges
def setUpModule():
testdata.init()
class WrapVariantCallingTest(absltest.TestCase):
def test_call_from_allele_counter(self):
ref = fasta.IndexedFastaReader(testdata.CHR20_FASTA)
sam_reader = sam.SamReader(testdata.CHR20_BAM)
size = 1000
region = ranges.make_range('chr20', 10000000, 10000000 + size)
allele_counter = _allelecounter.AlleleCounter(
ref.c_reader,
region,
[],
deepvariant_pb2.AlleleCounterOptions(partition_size=size),
)
caller = variant_calling_multisample.VariantCaller(
deepvariant_pb2.VariantCallerOptions(
min_count_snps=2,
min_count_indels=2,
min_fraction_snps=0.12,
min_fraction_indels=0.12,
sample_name='sample_name',
p_error=0.001,
max_gq=50,
gq_resolution=1,
ploidy=2,
)
)
# Grab all of the reads in our region and add them to the allele_counter.
reads = list(sam_reader.query(region))
self.assertNotEmpty(reads)
for read in reads:
allele_counter.add(read, 'sample_id')
# Get the candidates records for this whole region.
allele_counters = {}
allele_counters['sample_id'] = allele_counter
candidates = caller.calls_from_allele_counts(allele_counters, 'sample_id')
# We should have at least some candidates and some gvcf records.
self.assertNotEmpty(candidates)
# Each candidate should be a DeepVariantCall.
for candidate in candidates:
self.assertIsInstance(candidate, deepvariant_pb2.DeepVariantCall)
if __name__ == '__main__':
absltest.main()