def test_genotyping_trio5():
reads = """
B 101
B 101
B 101
A 111
A 111
A 111
C 111
C 111
C 101
C 101
"""
expected_genotypes = [
canonic_index_list_to_biallelic_gt_list([2, 2, 2]),
canonic_index_list_to_biallelic_gt_list([2, 0, 2]),
canonic_index_list_to_biallelic_gt_list([2, 1, 2]),
]
numeric_sample_ids = NumericSampleIds()
pedigree = Pedigree(numeric_sample_ids)
pedigree.add_individual(
"individual0",
canonic_index_list_to_biallelic_gt_list([0, 0, 0]),
[PhredGenotypeLikelihoods([1.0 / 3.0, 1.0 / 3.0, 1.0 / 3.0])] * 3,
)
pedigree.add_individual(
"individual1",
canonic_index_list_to_biallelic_gt_list([0, 0, 0]),
[PhredGenotypeLikelihoods([1.0 / 3.0, 1.0 / 3.0, 1.0 / 3.0])] * 3,
)
pedigree.add_individual(
"individual2",
canonic_index_list_to_biallelic_gt_list([0, 0, 0]),
[PhredGenotypeLikelihoods([1.0 / 3.0, 1.0 / 3.0, 1.0 / 3.0])] * 3,
)
pedigree.add_relationship("individual0", "individual1", "individual2")
recombcost = [2, 2, 2]
genotype_pedigree(numeric_sample_ids, reads, recombcost, pedigree, expected_genotypes)
def verify(rs, all_heterozygous=False):
positions = rs.get_positions()
recombcost = [1] * len(
positions) # recombination costs 1, should not occur
pedigree = Pedigree(NumericSampleIds())
genotype_likelihoods = [
None if all_heterozygous else PhredGenotypeLikelihoods(0, 0, 0)
] * len(positions)
pedigree.add_individual('individual0', [1] * len(positions),
genotype_likelihoods) # all genotypes heterozygous
dp_table = PedigreeDPTable(rs,
recombcost,
pedigree,
distrust_genotypes=not all_heterozygous)
verify_mec_score_and_partitioning(dp_table, rs)
def test_genotyping_trio14():
reads = """
A 111111
A 111111
B 111111
B 000000
C 000000
"""
expected_genotypes = [
canonic_index_list_to_biallelic_gt_list([2, 2, 2, 2, 2, 2]),
canonic_index_list_to_biallelic_gt_list([1, 1, 1, 1, 1, 1]),
canonic_index_list_to_biallelic_gt_list([1, 1, 1, 1, 1, 1]),
]
numeric_sample_ids = NumericSampleIds()
pedigree = Pedigree(numeric_sample_ids)
pedigree.add_individual(
"individual0",
canonic_index_list_to_biallelic_gt_list([0, 0, 0, 0, 0, 0]),
[PhredGenotypeLikelihoods([1 / 3.0, 1 / 3.0, 1 / 3.0])] * 6,
)
pedigree.add_individual(
"individual1",
canonic_index_list_to_biallelic_gt_list([0, 0, 0, 0, 0, 0]),
[PhredGenotypeLikelihoods([1 / 3.0, 1 / 3.0, 1 / 3.0])] * 6,
)
pedigree.add_individual(
"individual2",
canonic_index_list_to_biallelic_gt_list([0, 0, 0, 0, 0, 0]),
[PhredGenotypeLikelihoods([1 / 3.0, 1 / 3.0, 1 / 3.0])] * 6,
)
pedigree.add_relationship("individual0", "individual1", "individual2")
recombcost = [1000000, 1000000, 1000000, 1000000, 1000000, 1000000]
genotype_pedigree(
numeric_sample_ids, reads, recombcost, pedigree, expected_genotypes, scaling=1000,
)
def verify(rs, all_heterozygous=False):
positions = rs.get_positions()
# recombination costs 1, should not occur
recombcost = [1] * len(positions)
pedigree = Pedigree(NumericSampleIds())
genotype_likelihoods = [
None if all_heterozygous else PhredGenotypeLikelihoods([0, 0, 0])
] * len(positions)
# all genotypes heterozygous
pedigree.add_individual(
"individual0",
[canonic_index_to_biallelic_gt(1) for _ in range(len(positions))],
genotype_likelihoods,
)
dp_table = PedigreeDPTable(rs, recombcost, pedigree, distrust_genotypes=not all_heterozygous)
verify_mec_score_and_partitioning(dp_table, rs)
def check_genotyping_single_individual(reads, weights = None, expected = None, genotypes = None, scaling = None, genotype_priors = None):
# 0) set up read set
readset = string_to_readset(s=reads, w=weights, scale_quality=scaling)
positions = readset.get_positions()
# 1) Genotype using forward backward algorithm
recombcost = [1] * len(positions)
numeric_sample_ids = NumericSampleIds()
pedigree = Pedigree(numeric_sample_ids)
genotype_likelihoods = [PhredGenotypeLikelihoods(1.0/3.0,1.0/3.0,1.0/3.0)] * len(positions)
if genotype_priors != None:
genotype_likelihoods = genotype_priors
pedigree.add_individual('individual0', [1] * len(positions), genotype_likelihoods)
dp_forward_backward = GenotypeDPTable(numeric_sample_ids, readset, recombcost,pedigree)
# check the results
compare_to_expected(dp_forward_backward, positions, expected, genotypes)
def phase_MAV(reads, n_alleles, all_het, genos, genotypes, weights=None):
readset = string_to_readset(reads, n_alleles)
positions = readset.get_positions()
for all_heterozygous in all_het:
recombcost = [1] * len(
positions) # recombination costs 1, should not occur
pedigree = Pedigree(NumericSampleIds())
genotype_likelihoods = [
None if all_heterozygous else PhredGenotypeLikelihoods(genos)
] * len(positions)
pedigree.add_individual(
'individual0', genotypes,
genotype_likelihoods) # all genotypes heterozygous
dp_table = PedigreeDPTable(readset,
recombcost,
pedigree,
distrust_genotypes=not all_heterozygous)
superreads_list, transmission_vector = dp_table.get_super_reads()
cost = dp_table.get_optimal_cost()
return superreads_list, transmission_vector, cost
def create_pedigree(
default_gq,
distrust_genotypes,
family,
gl_regularizer,
numeric_sample_ids,
phasable_variant_table,
trios,
):
pedigree = Pedigree(numeric_sample_ids)
for sample in family:
# If distrusting genotypes, we pass genotype likelihoods on to pedigree object
if distrust_genotypes:
genotype_likelihoods = []
for gt, gl in zip(
phasable_variant_table.genotypes_of(sample),
phasable_variant_table.genotype_likelihoods_of(sample),
):
assert gt.is_diploid_and_biallelic()
if gl is None:
# all genotypes get default_gq as genotype likelihood, exept the called genotype ...
x = [default_gq] * 3
# ... which gets a 0
x[gt.get_index()] = 0
genotype_likelihoods.append(PhredGenotypeLikelihoods(x))
else:
genotype_likelihoods.append(
gl.as_phred(regularizer=gl_regularizer))
else:
genotype_likelihoods = None
pedigree.add_individual(sample,
phasable_variant_table.genotypes_of(sample),
genotype_likelihoods)
for trio in trios:
pedigree.add_relationship(father_id=trio.father,
mother_id=trio.mother,
child_id=trio.child)
return pedigree
def test_geno_10():
reads = """
001100
000000
000000
110011
110011
111111
"""
genotypes = canonic_index_list_to_biallelic_gt_list([1, 1, 0, 0, 1, 1])
genotype_priors = [
PhredGenotypeLikelihoods([0.1, 0.8, 0.1]),
PhredGenotypeLikelihoods([0.1, 0.8, 0.1]),
PhredGenotypeLikelihoods([0.7, 0.2, 0.1]),
PhredGenotypeLikelihoods([0.7, 0.2, 0.1]),
PhredGenotypeLikelihoods([0.1, 0.8, 0.1]),
PhredGenotypeLikelihoods([0.1, 0.8, 0.1]),
]
check_genotyping_single_individual(reads, None, None, genotypes, 50, genotype_priors)
def test_geno_priors2():
reads = """
11
01
"""
prior_likelihoods = [
PhredGenotypeLikelihoods([0, 0.5, 0.5]),
PhredGenotypeLikelihoods([0.25, 0.5, 0.25]),
PhredGenotypeLikelihoods([0.1, 0.4, 0.5]),
]
expected_likelihoods = [
PhredGenotypeLikelihoods([0.0, 0.35714285714285715, 0.6428571428571429]),
PhredGenotypeLikelihoods([0.1323529411764706, 0.7352941176470589, 0.1323529411764706]),
PhredGenotypeLikelihoods([0.015151515151515152, 0.30303030303030304, 0.6818181818181818]),
]
check_genotyping_single_individual(
reads, None, expected_likelihoods, None, 10, prior_likelihoods
)
def check_phasing_single_individual(reads, algorithm="whatshap", weights=None):
# 0) set up read set
readset = string_to_readset(reads, weights)
positions = readset.get_positions()
# for hapchat
if algorithm == "hapchat":
dp_table = HapChatCore(readset)
superreads = dp_table.get_super_reads()
cost = dp_table.get_optimal_cost()
partition = dp_table.get_optimal_partitioning()
compare_phasing_brute_force(superreads[0][0], cost, partition, readset,
True, weights, algorithm)
return
# 1) Phase using PedMEC code for single individual
for all_heterozygous in [False, True]:
recombcost = [1] * len(
positions) # recombination costs 1, should not occur
pedigree = Pedigree(NumericSampleIds())
genotype_likelihoods = [
None if all_heterozygous else PhredGenotypeLikelihoods([0, 0, 0])
] * len(positions)
pedigree.add_individual(
"individual0",
[canonic_index_to_biallelic_gt(1) for i in range(len(positions))],
genotype_likelihoods,
) # all genotypes heterozygous
dp_table = PedigreeDPTable(readset,
recombcost,
pedigree,
distrust_genotypes=not all_heterozygous)
superreads, transmission_vector = dp_table.get_super_reads()
cost = dp_table.get_optimal_cost()
# TODO: transmission vectors not returned properly, see issue 73
assert len(set(transmission_vector)) == 1
partition = dp_table.get_optimal_partitioning()
compare_phasing_brute_force(superreads[0], cost, partition, readset,
all_heterozygous, weights)
# 2) Phase using PedMEC code for trios with two "empty" individuals (i.e. having no reads)
for all_heterozygous in [False, True]:
recombcost = [1] * len(
positions) # recombination costs 1, should not occur
pedigree = Pedigree(NumericSampleIds())
genotype_likelihoods = [
None if all_heterozygous else PhredGenotypeLikelihoods([0, 0, 0])
] * len(positions)
pedigree.add_individual(
"individual0",
[canonic_index_to_biallelic_gt(1) for _ in range(len(positions))],
genotype_likelihoods,
) # all genotypes heterozygous
pedigree.add_individual(
"individual1",
[canonic_index_to_biallelic_gt(1) for _ in range(len(positions))],
genotype_likelihoods,
) # all genotypes heterozygous
pedigree.add_individual(
"individual2",
[canonic_index_to_biallelic_gt(1) for _ in range(len(positions))],
genotype_likelihoods,
) # all genotypes heterozygous
pedigree.add_relationship("individual0", "individual1", "individual2")
dp_table = PedigreeDPTable(readset,
recombcost,
pedigree,
distrust_genotypes=not all_heterozygous)
cost = dp_table.get_optimal_cost()
superreads, transmission_vector = dp_table.get_super_reads()
assert len(set(transmission_vector)) == 1
partition = dp_table.get_optimal_partitioning()
compare_phasing_brute_force(superreads[0], cost, partition, readset,
all_heterozygous, weights)
def run_genotype(
phase_input_files,
variant_file,
reference=None,
output=sys.stdout,
samples=None,
chromosomes=None,
ignore_read_groups=False,
indels=True,
mapping_quality=20,
max_coverage=15,
nopriors=False,
ped=None,
recombrate=1.26,
genmap=None,
gt_qual_threshold=0,
prioroutput=None,
constant=0.0,
overhang=10,
affine_gap=False,
gap_start=10,
gap_extend=7,
mismatch=15,
write_command_line_header=True,
use_ped_samples=False,
):
"""
For now: this function only runs the genotyping algorithm. Genotype likelihoods for
all variants are computed using the forward backward algorithm
"""
timers = StageTimer()
logger.info(
"This is WhatsHap (genotyping) %s running under Python %s",
__version__,
platform.python_version(),
)
if write_command_line_header:
command_line = "(whatshap {}) {}".format(__version__,
" ".join(sys.argv[1:]))
else:
command_line = None
with ExitStack() as stack:
# read the given input files (BAMs, VCFs, ref...)
numeric_sample_ids = NumericSampleIds()
phased_input_reader = stack.enter_context(
PhasedInputReader(
phase_input_files,
reference,
numeric_sample_ids,
ignore_read_groups,
indels=indels,
mapq_threshold=mapping_quality,
overhang=overhang,
affine=affine_gap,
gap_start=gap_start,
gap_extend=gap_extend,
default_mismatch=mismatch,
))
show_phase_vcfs = phased_input_reader.has_vcfs
# vcf writer for final genotype likelihoods
vcf_writer = stack.enter_context(
GenotypeVcfWriter(command_line=command_line,
in_path=variant_file,
out_file=output))
# vcf writer for only the prior likelihoods (if output is desired)
prior_vcf_writer = None
if prioroutput is not None:
prior_vcf_writer = stack.enter_context(
GenotypeVcfWriter(
command_line=command_line,
in_path=variant_file,
out_file=stack.enter_context(open(prioroutput, "w")),
))
# parse vcf with input variants
# remove all likelihoods that may already be present
vcf_reader = stack.enter_context(
VcfReader(
variant_file,
indels=indels,
genotype_likelihoods=False,
ignore_genotypes=True,
))
if ignore_read_groups and not samples and len(vcf_reader.samples) > 1:
raise CommandLineError(
"When using --ignore-read-groups on a VCF with "
"multiple samples, --sample must also be used.")
if not samples:
samples = vcf_reader.samples
# if --use-ped-samples is set, use only samples from PED file
if ped and use_ped_samples:
samples = set()
for trio in PedReader(ped):
if trio.child is None or trio.mother is None or trio.father is None:
continue
samples.add(trio.mother)
samples.add(trio.father)
samples.add(trio.child)
vcf_sample_set = set(vcf_reader.samples)
for sample in samples:
if sample not in vcf_sample_set:
raise CommandLineError(
"Sample {!r} requested on command-line not found in VCF".
format(sample))
if ped and genmap:
logger.info(
"Using region-specific recombination rates from genetic map %s.",
genmap,
)
recombination_cost_computer = GeneticMapRecombinationCostComputer(
genmap)
else:
if ped:
logger.info("Using uniform recombination rate of %g cM/Mb.",
recombrate)
recombination_cost_computer = UniformRecombinationCostComputer(
recombrate)
samples = frozenset(samples)
families, family_trios = setup_families(samples, ped,
numeric_sample_ids,
max_coverage)
# Read phase information provided as VCF files, if provided.
with timers("parse_phasing_vcfs"):
phased_input_reader.read_vcfs()
# compute genotype likelihood threshold
gt_prob = 1.0 - (10**(-gt_qual_threshold / 10.0))
for variant_table in timers.iterate("parse_vcf", vcf_reader):
# create a mapping of genome positions to indices
var_to_pos = dict()
for i in range(len(variant_table.variants)):
var_to_pos[variant_table.variants[i].position] = i
chromosome = variant_table.chromosome
if (not chromosomes) or (chromosome in chromosomes):
logger.info("======== Working on chromosome %r", chromosome)
else:
logger.info(
"Leaving chromosome %r unchanged (present in VCF but not requested by option --chromosome)",
chromosome,
)
vcf_writer.write_genotypes(chromosome,
variant_table,
indels,
leave_unchanged=True)
if prioroutput is not None:
prior_vcf_writer.write_genotypes(chromosome,
variant_table,
indels,
leave_unchanged=True)
continue
positions = [v.position for v in variant_table.variants]
if not nopriors:
# compute prior genotype likelihoods based on all reads
for sample in samples:
logger.info("---- Initial genotyping of %s", sample)
with timers("read_bam"):
readset, vcf_source_ids = phased_input_reader.read(
chromosome,
variant_table.variants,
sample,
read_vcf=False,
)
readset.sort()
genotypes, genotype_likelihoods = compute_genotypes(
readset, positions)
# recompute genotypes based on given threshold
reg_genotype_likelihoods = []
for gl in range(len(genotype_likelihoods)):
norm_sum = (genotype_likelihoods[gl][0] +
genotype_likelihoods[gl][1] +
genotype_likelihoods[gl][2] +
3 * constant)
regularized = PhredGenotypeLikelihoods([
(genotype_likelihoods[gl][0] + constant) /
norm_sum,
(genotype_likelihoods[gl][1] + constant) /
norm_sum,
(genotype_likelihoods[gl][2] + constant) /
norm_sum,
])
genotypes[gl] = determine_genotype(
regularized, gt_prob)
assert isinstance(genotypes[gl], Genotype)
reg_genotype_likelihoods.append(regularized)
variant_table.set_genotype_likelihoods_of(
sample,
[
PhredGenotypeLikelihoods(list(gl))
for gl in reg_genotype_likelihoods
],
)
variant_table.set_genotypes_of(sample, genotypes)
else:
# use uniform genotype likelihoods for all individuals
for sample in samples:
variant_table.set_genotype_likelihoods_of(
sample,
[PhredGenotypeLikelihoods([1 / 3, 1 / 3, 1 / 3])] *
len(positions),
)
# if desired, output the priors in separate vcf
if prioroutput is not None:
prior_vcf_writer.write_genotypes(chromosome, variant_table,
indels)
# Iterate over all families to process, i.e. a separate DP table is created
# for each family.
for representative_sample, family in sorted(families.items()):
if len(family) == 1:
logger.info("---- Processing individual %s",
representative_sample)
else:
logger.info("---- Processing family with individuals: %s",
",".join(family))
max_coverage_per_sample = max(1, max_coverage // len(family))
logger.info("Using maximum coverage per sample of %dX",
max_coverage_per_sample)
trios = family_trios[representative_sample]
assert (len(family) == 1) or (len(trios) > 0)
# Get the reads belonging to each sample
readsets = dict()
for sample in family:
with timers("read_bam"):
readset, vcf_source_ids = phased_input_reader.read(
chromosome,
variant_table.variants,
sample,
)
with timers("select"):
readset = readset.subset([
i for i, read in enumerate(readset)
if len(read) >= 2
])
logger.info(
"Kept %d reads that cover at least two variants each",
len(readset),
)
selected_reads = select_reads(
readset,
max_coverage_per_sample,
preferred_source_ids=vcf_source_ids,
)
readsets[sample] = selected_reads
# Merge reads into one ReadSet (note that each Read object
# knows the sample it originated from).
all_reads = ReadSet()
for sample, readset in readsets.items():
for read in readset:
assert read.is_sorted(), "Add a read.sort() here"
all_reads.add(read)
all_reads.sort()
# Determine which variants can (in principle) be phased
accessible_positions = sorted(all_reads.get_positions())
logger.info(
"Variants covered by at least one phase-informative "
"read in at least one individual after read selection: %d",
len(accessible_positions),
)
# Create Pedigree
pedigree = Pedigree(numeric_sample_ids)
for sample in family:
# genotypes are assumed to be unknown, so ignore information that
# might already be present in the input vcf
all_genotype_likelihoods = variant_table.genotype_likelihoods_of(
sample)
genotype_l = [
all_genotype_likelihoods[var_to_pos[a_p]]
for a_p in accessible_positions
]
pedigree.add_individual(
sample,
[
Genotype([])
for i in range(len(accessible_positions))
],
genotype_l,
)
for trio in trios:
pedigree.add_relationship(
father_id=trio.father,
mother_id=trio.mother,
child_id=trio.child,
)
recombination_costs = recombination_cost_computer.compute(
accessible_positions)
# Finally, run genotyping algorithm
with timers("genotyping"):
problem_name = "genotyping"
logger.info(
"Genotype %d sample%s by solving the %s problem ...",
len(family),
"s" if len(family) > 1 else "",
problem_name,
)
forward_backward_table = GenotypeDPTable(
numeric_sample_ids,
all_reads,
recombination_costs,
pedigree,
accessible_positions,
)
# store results
for s in family:
likelihood_list = variant_table.genotype_likelihoods_of(
s)
genotypes_list = variant_table.genotypes_of(s)
for pos in range(len(accessible_positions)):
likelihoods = forward_backward_table.get_genotype_likelihoods(
s, pos)
# compute genotypes from likelihoods and store information
geno = determine_genotype(likelihoods, gt_prob)
assert isinstance(geno, Genotype)
genotypes_list[var_to_pos[
accessible_positions[pos]]] = geno
likelihood_list[var_to_pos[
accessible_positions[pos]]] = likelihoods
variant_table.set_genotypes_of(s, genotypes_list)
variant_table.set_genotype_likelihoods_of(
s, likelihood_list)
with timers("write_vcf"):
logger.info("======== Writing VCF")
vcf_writer.write_genotypes(chromosome, variant_table, indels)
logger.info("Done writing VCF")
logger.debug("Chromosome %r finished", chromosome)
logger.info("\n== SUMMARY ==")
total_time = timers.total()
log_memory_usage()
logger.info(
"Time spent reading BAM: %6.1f s",
timers.elapsed("read_bam"),
)
logger.info(
"Time spent parsing VCF: %6.1f s",
timers.elapsed("parse_vcf"),
)
if show_phase_vcfs:
logger.info(
"Time spent parsing input phasings from VCFs: %6.1f s",
timers.elapsed("parse_phasing_vcfs"),
)
logger.info("Time spent selecting reads: %6.1f s",
timers.elapsed("select"))
logger.info(
"Time spent genotyping: %6.1f s",
timers.elapsed("genotyping"),
)
logger.info(
"Time spent writing VCF: %6.1f s",
timers.elapsed("write_vcf"),
)
logger.info(
"Time spent on rest: %6.1f s",
total_time - timers.sum(),
)
logger.info("Total elapsed time: %6.1f s",
total_time)
def test_genotype_likelihoods():
assert list(PhredGenotypeLikelihoods()) == [0, 0, 0]
assert list(PhredGenotypeLikelihoods(7, 1, 12)) == [7, 1, 12]
gl = GenotypeLikelihoods(*(math.log10(x) for x in [1e-10, 0.5, 0.002]))
assert list(gl.as_phred()) == [97, 0, 24]
assert list(gl.as_phred(regularizer=0.01)) == [20, 0, 19]