def main(args):
mt = get_gnomad_v3_mt(key_by_locus_and_alleles=True)
mt = mt.annotate_entries(
gvcf_info=mt.gvcf_info.drop('ClippingRankSum', 'ReadPosRankSum'))
mt = mt.annotate_rows(
n_unsplit_alleles=hl.len(mt.alleles),
mixed_site=(hl.len(mt.alleles) > 2)
& hl.any(lambda a: hl.is_indel(mt.alleles[0], a), mt.alleles[1:])
& hl.any(lambda a: hl.is_snp(mt.alleles[0], a), mt.alleles[1:]))
mt = hl.experimental.sparse_split_multi(mt, filter_changed_loci=True)
mt.write(args.split_mt_location, overwrite=args.overwrite)
def get_gene_intervals(gene_symbols=None, gene_ids=None, transcript_ids=None,
verbose=True, reference_genome=None, gtf_file=None):
"""Get intervals of genes or transcripts.
Get the boundaries of genes or transcripts from a GTF file, for quick filtering of a Table or MatrixTable.
On Google Cloud platform:
Gencode v19 (GRCh37) GTF available at: gs://hail-common/references/gencode/gencode.v19.annotation.gtf.bgz
Gencode v29 (GRCh38) GTF available at: gs://hail-common/references/gencode/gencode.v29.annotation.gtf.bgz
Example
-------
>>> hl.filter_intervals(ht, get_gene_intervals(gene_symbols=['PCSK9'], reference_genome='GRCh37')) # doctest: +SKIP
Parameters
----------
gene_symbols : :obj:`list` of :obj:`str`, optional
Gene symbols (e.g. PCSK9).
gene_ids : :obj:`list` of :obj:`str`, optional
Gene IDs (e.g. ENSG00000223972).
transcript_ids : :obj:`list` of :obj:`str`, optional
Transcript IDs (e.g. ENSG00000223972).
verbose : :obj:`bool`
If ``True``, print which genes and transcripts were matched in the GTF file.
reference_genome : :obj:`str` or :class:`.ReferenceGenome`, optional
Reference genome to use (passed along to import_gtf).
gtf_file : :obj:`str`
GTF file to load. If none is provided, but `reference_genome` is one of
`GRCh37` or `GRCh38`, a default will be used (on Google Cloud Platform).
Returns
-------
:obj:`list` of :class:`.Interval`
"""
if gene_symbols is None and gene_ids is None and transcript_ids is None:
raise ValueError('get_gene_intervals requires at least one of gene_symbols, gene_ids, or transcript_ids')
ht = _load_gencode_gtf(gtf_file, reference_genome)
criteria = []
if gene_symbols:
criteria.append(hl.any(lambda y: (ht.feature == 'gene') & (ht.gene_name == y), gene_symbols))
if gene_ids:
criteria.append(hl.any(lambda y: (ht.feature == 'gene') & (ht.gene_id == y.split('\\.')[0]), gene_ids))
if transcript_ids:
criteria.append(hl.any(lambda y: (ht.feature == 'transcript') & (ht.transcript_id == y.split('\\.')[0]), transcript_ids))
ht = ht.filter(functools.reduce(operator.ior, criteria))
gene_info = ht.aggregate(hl.agg.collect((ht.feature, ht.gene_name, ht.gene_id, ht.transcript_id, ht.interval)))
if verbose:
info(f'get_gene_intervals found {len(gene_info)} entries:\n'
+ "\n".join(map(lambda x: f'{x[0]}: {x[1]} ({x[2] if x[0] == "gene" else x[3]})', gene_info)))
intervals = list(map(lambda x: x[-1], gene_info))
return intervals
def get_gnomad_v3_mt(
split=False,
key_by_locus_and_alleles: bool = False,
remove_hard_filtered_samples: bool = True,
release_only: bool = False,
samples_meta: bool = False,
) -> hl.MatrixTable:
"""
Wrapper function to get gnomAD data with desired filtering and metadata annotations
:param split: Perform split on MT - Note: this will perform a split on the MT rather than grab an already split MT
:param key_by_locus_and_alleles: Whether to key the MatrixTable by locus and alleles (only needed for v3)
:param remove_hard_filtered_samples: Whether to remove samples that failed hard filters (only relevant after sample QC)
:param release_only: Whether to filter the MT to only samples available for release (can only be used if metadata is present)
:param samples_meta: Whether to add metadata to MT in 'meta' column
:return: gnomAD v3 dataset with chosen annotations and filters
"""
mt = gnomad_v3_genotypes.mt()
if key_by_locus_and_alleles:
mt = hl.MatrixTable(
hl.ir.MatrixKeyRowsBy(
mt._mir, ["locus", "alleles"], is_sorted=True
) # Prevents hail from running sort on genotype MT which is already sorted by a unique locus
)
if remove_hard_filtered_samples:
mt = mt.filter_cols(
hl.is_missing(hard_filtered_samples.ht()[mt.col_key]))
if samples_meta:
mt = mt.annotate_cols(meta=meta.ht()[mt.col_key])
if release_only:
mt = mt.filter_cols(mt.meta.release)
elif release_only:
mt = mt.filter_cols(meta.ht()[mt.col_key].release)
if split:
mt = mt.annotate_rows(
n_unsplit_alleles=hl.len(mt.alleles),
mixed_site=(hl.len(mt.alleles) > 2)
& hl.any(lambda a: hl.is_indel(mt.alleles[0], a), mt.alleles[1:])
& hl.any(lambda a: hl.is_snp(mt.alleles[0], a), mt.alleles[1:]),
)
mt = hl.experimental.sparse_split_multi(mt, filter_changed_loci=True)
return mt
def generate_allele_data(mt: hl.MatrixTable) -> hl.Table:
"""
Writes bi-allelic sites MT with the following annotations:
- allele_data (nonsplit_alleles, has_star, variant_type, and n_alt_alleles)
:param MatrixTable mt: Full unsplit MT
:return: Table with allele data annotations
:rtype: Table
"""
ht = mt.rows().select()
allele_data = hl.struct(nonsplit_alleles=ht.alleles,
has_star=hl.any(lambda a: a == '*', ht.alleles))
ht = ht.annotate(allele_data=allele_data.annotate(
**add_variant_type(ht.alleles)))
ht = hl.split_multi_hts(ht)
allele_type = (hl.case().when(
hl.is_snp(ht.alleles[0], ht.alleles[1]),
'snv').when(hl.is_insertion(ht.alleles[0], ht.alleles[1]),
'ins').when(hl.is_deletion(ht.alleles[0], ht.alleles[1]),
'del').default('complex'))
ht = ht.annotate(allele_data=ht.allele_data.annotate(
allele_type=allele_type,
was_mixed=ht.allele_data.variant_type == 'mixed'))
return ht
def get_filtered_mt(chrom: str = 'all',
pop: str = 'all',
imputed: bool = True,
min_mac: int = 20,
entry_fields=('GP', )):
if imputed:
ht = hl.read_table(get_ukb_af_ht_path())
if pop == 'all':
ht = ht.filter(
hl.any(lambda x: ht.af[x] * ht.an[x] >= min_mac,
hl.literal(POPS)))
else:
ht = ht.filter(ht.af[pop] * ht.an[pop] >= min_mac)
mt = get_ukb_imputed_data(chrom,
variant_list=ht,
entry_fields=entry_fields)
else:
mt = hl.read_matrix_table('gs://ukb31063/ukb31063.genotype.mt')
covariates_ht = get_covariates()
hq_samples_ht = get_hq_samples()
# TODO: confirm that this is correct set
mt = mt.annotate_cols(**covariates_ht[mt.s])
mt = mt.filter_cols(
hl.is_defined(mt.pop) & hl.is_defined(hq_samples_ht[mt.s]))
if pop != 'all': mt = mt.filter_cols(mt.pop == pop)
return mt
def generate_allele_data(ht: hl.Table) -> hl.Table:
"""
Returns bi-allelic sites HT with the following annotations:
- allele_data (nonsplit_alleles, has_star, variant_type, and n_alt_alleles)
:param Table ht: Full unsplit HT
:return: Table with allele data annotations
:rtype: Table
"""
ht = ht.select()
allele_data = hl.struct(nonsplit_alleles=ht.alleles,
has_star=hl.any(lambda a: a == "*", ht.alleles))
ht = ht.annotate(allele_data=allele_data.annotate(
**add_variant_type(ht.alleles)))
ht = hl.split_multi_hts(ht)
ht = ht.filter(hl.len(ht.alleles) > 1)
allele_type = (hl.case().when(
hl.is_snp(ht.alleles[0], ht.alleles[1]),
"snv").when(hl.is_insertion(ht.alleles[0], ht.alleles[1]),
"ins").when(hl.is_deletion(ht.alleles[0], ht.alleles[1]),
"del").default("complex"))
ht = ht.annotate(allele_data=ht.allele_data.annotate(
allele_type=allele_type,
was_mixed=ht.allele_data.variant_type == "mixed"))
return ht
def conditional_phenotypes(mt: hl.MatrixTable,
column_field,
entry_field,
lists_of_columns,
new_col_name='grouping',
new_entry_name='new_entry'):
"""
Create a conditional phenotype by setting phenotype1 to missing for any individual without phenotype2.
Pheno1 Pheno2 new_pheno
T T T
T F NA
F F NA
F T F
`lists_of_columns` should be a list of lists (of length 2 for the inner list).
The first element corresponds to the phenotype to maintain, except for setting to missing when the
phenotype coded by the second element is False.
new_entry = Pheno1 conditioned on having Pheno2
Example:
mt = hl.balding_nichols_model(1, 3, 10).drop('GT')
mt = mt.annotate_entries(pheno=hl.rand_bool(0.5))
lists_of_columns = [[0, 1], [2, 1]]
entry_field = mt.pheno
column_field = mt.sample_idx
:param MatrixTable mt: Input MatrixTable
:param Expression column_field: Column-indexed Expression to group by
:param Expression entry_field: Entry-indexed Expression to which to apply `grouping_function`
:param list of list lists_of_columns: Entry in this list should be the same type as `column_field`
:param str new_col_name: Name for new column key (default 'grouping')
:param str new_entry_name: Name for new entry expression (default 'new_entry')
:return: Re-grouped MatrixTable
:rtype: MatrixTable
"""
assert all([len(x) == 2 for x in lists_of_columns])
lists_of_columns = hl.literal(lists_of_columns)
mt = mt._annotate_all(col_exprs={'_col_expr': column_field},
entry_exprs={'_entry_expr': entry_field})
mt = mt.annotate_cols(
_col_expr=lists_of_columns.filter(lambda x: x.contains(
mt._col_expr)).map(lambda y: (y, y[0] == mt._col_expr)))
mt = mt.explode_cols('_col_expr')
# if second element (~mt._col_expr[1]) is false (~mt._entry_expr), then return missing
# otherwise, get actual element (either true if second element, or actual first element)
bool_array = hl.agg.collect(
hl.if_else(~mt._col_expr[1] & ~mt._entry_expr, hl.null(hl.tbool),
mt._entry_expr))
# if any element is missing, return missing. otherwise return first element
return mt.group_cols_by(**{
new_col_name: mt._col_expr[0]
}).aggregate(
**{
new_entry_name:
hl.if_else(hl.any(lambda x: hl.is_missing(x), bool_array),
hl.null(hl.tbool), bool_array[0] & bool_array[1])
})
def generate_split_alleles(mt: hl.MatrixTable) -> hl.Table:
allele_data = hl.struct(nonsplit_alleles=mt.alleles,
has_star=hl.any(lambda a: a == '*', mt.alleles))
mt = mt.annotate_rows(allele_data=allele_data.annotate(
**add_variant_type(mt.alleles)))
mt = hl.split_multi_hts(mt, left_aligned=True)
allele_type = (hl.case().when(
hl.is_snp(mt.alleles[0], mt.alleles[1]),
'snv').when(hl.is_insertion(mt.alleles[0], mt.alleles[1]),
'ins').when(hl.is_deletion(mt.alleles[0], mt.alleles[1]),
'del').default('complex'))
mt = mt.annotate_rows(allele_data=mt.allele_data.annotate(
allele_type=allele_type,
was_mixed=mt.allele_data.variant_type == 'mixed'))
return mt
def get_filtered_mt(pop: str = 'all',
imputed: bool = True,
chrom: str = 'all',
min_mac: int = 20):
if imputed:
ht = hl.read_table(ukb_af_ht_path)
if pop == 'all':
ht = ht.filter(
hl.any(lambda x: ht.af[x] * ht.an[x] >= min_mac,
hl.literal(POPS)))
else:
ht = ht.filter(ht.af[pop] * ht.an[pop] >= min_mac)
mt = get_ukb_imputed_data(chrom, variant_list=ht)
else:
mt = hl.read_matrix_table('gs://ukb31063/ukb31063.genotype.mt')
meta_ht = get_ukb_meta()
mt = mt.annotate_cols(**meta_ht.key_by(s=hl.str(meta_ht.s))[mt.s])
if pop != 'all': mt = mt.filter_cols(mt.pop == pop)
return mt
def all_and_leave_one_out(x,
pop_array,
all_f=hl.sum,
loo_f=lambda i, x: hl.sum(x) - hl.or_else(x[i], 0)):
"""
Applies a function to an input array for all populations, and for each of leave-one-out populations.
:param x: Input array
:param pop_array: Population array
:param all_f: Function for all populations. It takes the input array and returns a new value
:param loo_f: Function for each of leave-one-out populations. It takes an index of leave-one-out
population and the input array, and returns an array of new values.
...
:return: Array of new values for all populations and for each of leave-one-out populations.
:rtype: ArrayExpression
"""
arr = hl.array([all_f(x)])
arr = arr.extend(hl.map(lambda i: loo_f(i, x),
hl.range(hl.len(pop_array))))
return hl.or_missing(hl.any(hl.is_defined, x), arr)
def get_r_within_gene(
bm: BlockMatrix,
ld_index: hl.Table,
gene: str,
vep_ht: hl.Table = None,
reference_genome: str = None,
):
"""
Get LD information (`r`) for all pairs of variants within `gene`.
Warning: this returns a table quadratic in number of variants. Exercise caution with large genes.
:param bm: Input Block Matrix
:param ld_index: Corresponding index table
:param gene: Gene symbol as string
:param vep_ht: Table with VEP annotations (if None, gets from get_gnomad_public_data())
:param reference_genome: Reference genome to pass to get_gene_intervals for fast filtering to gene
:return: Table with pairs of variants
"""
if vep_ht is None:
vep_ht = public_release("exomes").ht()
if reference_genome is None:
reference_genome = hl.default_reference().name
intervals = hl.experimental.get_gene_intervals(
gene_symbols=[gene], reference_genome=reference_genome)
ld_index = hl.filter_intervals(ld_index, intervals)
ld_index = ld_index.annotate(vep=vep_ht[ld_index.key].vep)
ld_index = ld_index.filter(
hl.any(lambda tc: tc.gene_symbol == gene,
ld_index.vep.transcript_consequences))
indices_to_keep = ld_index.idx.collect()
filt_bm = bm.filter(indices_to_keep, indices_to_keep)
ht = filt_bm.entries()
ld_index = ld_index.add_index("new_idx").key_by("new_idx")
return ht.transmute(r=ht.entry,
i_variant=ld_index[ht.i],
j_variant=ld_index[ht.j])
def get_filtered_mt(chrom: str = 'all',
pop: str = 'all',
imputed: bool = True,
min_mac: int = 20,
entry_fields=('GP', ),
filter_mac_instead_of_ac: bool = False):
# get ac or mac based on filter_mac_instead_of_ac
def get_ac(af, an):
if filter_mac_instead_of_ac:
# Note that the underlying file behind get_ukb_af_ht_path() accidentally double af and halve an
return (1.0 - hl.abs(1.0 - af)) * an
else:
return af * an
if imputed:
ht = hl.read_table(get_ukb_af_ht_path())
if pop == 'all':
ht = ht.filter(
hl.any(lambda x: get_ac(ht.af[x], ht.an[x]) >= min_mac,
hl.literal(POPS)))
else:
ht = ht.filter(get_ac(ht.af[pop], ht.an[pop]) >= min_mac)
mt = get_ukb_imputed_data(chrom,
variant_list=ht,
entry_fields=entry_fields)
else:
mt = hl.read_matrix_table('gs://ukb31063/ukb31063.genotype.mt')
covariates_ht = get_covariates()
hq_samples_ht = get_hq_samples()
mt = mt.annotate_cols(**covariates_ht[mt.s])
mt = mt.filter_cols(
hl.is_defined(mt.pop) & hl.is_defined(hq_samples_ht[mt.s]))
if pop != 'all': mt = mt.filter_cols(mt.pop == pop)
return mt
def process_consequences(mt: hl.MatrixTable,
vep_root: str = 'vep',
penalize_flags: bool = True) -> hl.MatrixTable:
"""
Adds most_severe_consequence (worst consequence for a transcript) into [vep_root].transcript_consequences,
and worst_csq_by_gene, any_lof into [vep_root]
:param MatrixTable mt: Input MT
:param str vep_root: Root for vep annotation (probably vep)
:param bool penalize_flags: Whether to penalize LOFTEE flagged variants, or treat them as equal to HC
:return: MT with better formatted consequences
:rtype: MatrixTable
"""
csqs = hl.literal(CSQ_ORDER)
csq_dict = hl.literal(dict(zip(CSQ_ORDER, range(len(CSQ_ORDER)))))
def add_most_severe_consequence(
tc: hl.expr.StructExpression) -> hl.expr.StructExpression:
"""
Add most_severe_consequence annotation to transcript consequences
This is for a given transcript, as there are often multiple annotations for a single transcript:
e.g. splice_region_variant&intron_variant -> splice_region_variant
"""
return tc.annotate(most_severe_consequence=csqs.find(
lambda c: tc.consequence_terms.contains(c)))
def find_worst_transcript_consequence(
tcl: hl.expr.ArrayExpression) -> hl.expr.StructExpression:
"""
Gets worst transcript_consequence from an array of em
"""
flag_score = 500
no_flag_score = flag_score * (1 + penalize_flags)
def csq_score(tc):
return csq_dict[csqs.find(
lambda x: x == tc.most_severe_consequence)]
tcl = tcl.map(lambda tc: tc.annotate(
csq_score=hl.case(missing_false=True).
when((tc.lof == 'HC') & (tc.lof_flags == ''),
csq_score(tc) - no_flag_score).when(
(tc.lof == 'HC') & (tc.lof_flags != ''),
csq_score(tc) - flag_score).when(tc.lof == 'LC',
csq_score(tc) - 10).
when(tc.polyphen_prediction == 'probably_damaging',
csq_score(tc) - 0.5).when(
tc.polyphen_prediction == 'possibly_damaging',
csq_score(tc) - 0.25).when(
tc.polyphen_prediction == 'benign',
csq_score(tc) - 0.1).default(csq_score(tc))))
return hl.or_missing(
hl.len(tcl) > 0,
hl.sorted(tcl, lambda x: x.csq_score)[0])
transcript_csqs = mt[vep_root].transcript_consequences.map(
add_most_severe_consequence)
gene_dict = transcript_csqs.group_by(lambda tc: tc.gene_symbol)
worst_csq_gene = gene_dict.map_values(find_worst_transcript_consequence)
sorted_scores = hl.sorted(worst_csq_gene.values(),
key=lambda tc: tc.csq_score)
lowest_score = hl.or_missing(
hl.len(sorted_scores) > 0, sorted_scores[0].csq_score)
gene_with_worst_csq = sorted_scores.filter(
lambda tc: tc.csq_score == lowest_score).map(lambda tc: tc.gene_symbol)
ensg_with_worst_csq = sorted_scores.filter(
lambda tc: tc.csq_score == lowest_score).map(lambda tc: tc.gene_id)
vep_data = mt[vep_root].annotate(
transcript_consequences=transcript_csqs,
worst_csq_by_gene=worst_csq_gene,
any_lof=hl.any(lambda x: x.lof == 'HC', worst_csq_gene.values()),
gene_with_most_severe_csq=gene_with_worst_csq,
ensg_with_most_severe_csq=ensg_with_worst_csq)
return mt.annotate_rows(**{vep_root: vep_data})
def main(args):
subsets = args.subsets
hl.init(
log=
f"/generate_frequency_data{'.' + '_'.join(subsets) if subsets else ''}.log",
default_reference="GRCh38",
)
invalid_subsets = []
n_subsets_use_subpops = 0
for s in subsets:
if s not in SUBSETS:
invalid_subsets.append(s)
if s in COHORTS_WITH_POP_STORED_AS_SUBPOP:
n_subsets_use_subpops += 1
if invalid_subsets:
raise ValueError(
f"{', '.join(invalid_subsets)} subset(s) are not one of the following official subsets: {SUBSETS}"
)
if n_subsets_use_subpops & (n_subsets_use_subpops != len(subsets)):
raise ValueError(
f"All or none of the supplied subset(s) should be in the list of cohorts that need to use subpops instead "
f"of pops in frequency calculations: {COHORTS_WITH_POP_STORED_AS_SUBPOP}"
)
try:
logger.info("Reading full sparse MT and metadata table...")
mt = get_gnomad_v3_mt(
key_by_locus_and_alleles=True,
release_only=not args.include_non_release,
samples_meta=True,
)
if args.test:
logger.info("Filtering to two partitions on chr20")
mt = hl.filter_intervals(
mt, [hl.parse_locus_interval("chr20:1-1000000")])
mt = mt._filter_partitions(range(2))
mt = hl.experimental.sparse_split_multi(mt, filter_changed_loci=True)
if args.include_non_release:
logger.info("Filtering MT columns to high quality samples")
total_sample_count = mt.count_cols()
mt = mt.filter_cols(mt.meta.high_quality)
high_quality_sample_count = mt.count_cols()
logger.info(
f"Filtered {total_sample_count - high_quality_sample_count} from the full set of {total_sample_count} "
f"samples...")
if subsets:
mt = mt.filter_cols(hl.any([mt.meta.subsets[s] for s in subsets]))
logger.info(
f"Running frequency generation pipeline on {mt.count_cols()} samples in {', '.join(subsets)} subset(s)..."
)
else:
logger.info(
f"Running frequency generation pipeline on {mt.count_cols()} samples..."
)
logger.info("Computing adj and sex adjusted genotypes...")
mt = mt.annotate_entries(
GT=adjusted_sex_ploidy_expr(mt.locus, mt.GT,
mt.meta.sex_imputation.sex_karyotype),
adj=get_adj_expr(mt.GT, mt.GQ, mt.DP, mt.AD),
)
logger.info("Densify-ing...")
mt = hl.experimental.densify(mt)
mt = mt.filter_rows(hl.len(mt.alleles) > 1)
# Temporary hotfix for depletion of homozygous alternate genotypes
logger.info(
"Setting het genotypes at sites with >1% AF (using v3.0 frequencies) and > 0.9 AB to homalt..."
)
# Load v3.0 allele frequencies to avoid an extra frequency calculation
# NOTE: Using previous callset AF works for small incremental changes to a callset, but we will need to revisit for large increments
freq_ht = get_freq(version="3").ht()
freq_ht = freq_ht.select(AF=freq_ht.freq[0].AF)
mt = mt.annotate_entries(GT=hl.cond(
(freq_ht[mt.row_key].AF > 0.01)
& mt.GT.is_het()
& (mt.AD[1] / mt.DP > 0.9),
hl.call(1, 1),
mt.GT,
))
logger.info("Generating frequency data...")
if subsets:
mt = annotate_freq(
mt,
sex_expr=mt.meta.sex_imputation.sex_karyotype,
pop_expr=mt.meta.population_inference.pop
if not n_subsets_use_subpops else
mt.meta.project_meta.project_subpop,
# NOTE: TGP and HGDP labeled populations are highly specific and are stored in the project_subpop meta field
)
# NOTE: no FAFs or popmax needed for subsets
mt = mt.select_rows("freq")
logger.info(
f"Writing out frequency data for {', '.join(subsets)} subset(s)..."
)
if args.test:
mt.rows().write(
get_checkpoint_path(
f"chr20_test_freq.{'_'.join(subsets)}"),
overwrite=True,
)
else:
mt.rows().write(get_freq(subset="_".join(subsets)).path,
overwrite=args.overwrite)
else:
logger.info("Computing age histograms for each variant...")
mt = mt.annotate_cols(age=hl.if_else(
hl.is_defined(mt.meta.project_meta.age),
mt.meta.project_meta.age,
mt.meta.project_meta.age_alt,
# NOTE: most age data is stored as integers in 'age' annotation, but for a select number of samples, age is stored as a bin range and 'age_alt' corresponds to an integer in the middle of the bin
))
mt = mt.annotate_rows(**age_hists_expr(mt.adj, mt.GT, mt.age))
# Compute callset-wide age histogram global
mt = mt.annotate_globals(age_distribution=mt.aggregate_cols(
hl.agg.hist(mt.age, 30, 80, 10)))
mt = annotate_freq(
mt,
sex_expr=mt.meta.sex_imputation.sex_karyotype,
pop_expr=mt.meta.population_inference.pop,
downsamplings=DOWNSAMPLINGS,
)
# Remove all loci with raw AC=0
mt = mt.filter_rows(mt.freq[1].AC > 0)
logger.info("Calculating InbreedingCoeff...")
# NOTE: This is not the ideal location to calculate this, but added here to avoid another densify
mt = mt.annotate_rows(
InbreedingCoeff=bi_allelic_site_inbreeding_expr(mt.GT))
logger.info("Computing filtering allele frequencies and popmax...")
faf, faf_meta = faf_expr(mt.freq, mt.freq_meta, mt.locus,
POPS_TO_REMOVE_FOR_POPMAX)
mt = mt.select_rows(
"InbreedingCoeff",
"freq",
faf=faf,
popmax=pop_max_expr(mt.freq, mt.freq_meta,
POPS_TO_REMOVE_FOR_POPMAX),
)
mt = mt.annotate_globals(
faf_meta=faf_meta,
faf_index_dict=make_faf_index_dict(faf_meta))
mt = mt.annotate_rows(popmax=mt.popmax.annotate(
faf95=mt.faf[mt.faf_meta.index(
lambda x: x.values() == ["adj", mt.popmax.pop])].faf95))
logger.info("Annotating quality metrics histograms...")
# NOTE: these are performed here as the quality metrics histograms also require densifying
mt = mt.annotate_rows(
qual_hists=qual_hist_expr(mt.GT, mt.GQ, mt.DP, mt.AD, mt.adj))
ht = mt.rows()
ht = ht.annotate(
qual_hists=hl.Struct(
**{
i.replace("_adj", ""): ht.qual_hists[i]
for i in ht.qual_hists if "_adj" in i
}),
raw_qual_hists=hl.Struct(**{
i: ht.qual_hists[i]
for i in ht.qual_hists if "_adj" not in i
}),
)
logger.info("Writing out frequency data...")
if args.test:
ht.write(get_checkpoint_path("chr20_test_freq"),
overwrite=True)
else:
ht.write(get_freq().path, overwrite=args.overwrite)
finally:
logger.info("Copying hail log to logging bucket...")
hl.copy_log(f"{qc_temp_prefix()}logs/")
# Mixture of non-empty with empty PL fields causes problems with sample QC for some reason; setting field to all empty mt = mt.annotate_entries(PL=hl.missing(mt.PL.dtype)) # Add variant-level annotations necessary for variant QC later ## Annotate variants in one of the categories: SNV, multi-SNV, indel, multi-indel, mixed mt = mt.annotate_rows(**add_variant_type(mt.alleles)) ## Number of alleles at the site mt = mt.annotate_rows(n_alleles = hl.len(mt.alleles)) ## Mixed sites (SNVs and indels present at the site) mt = mt.annotate_rows(mixed_site = hl.if_else(mt.variant_type == "mixed", True, False)) ## Spanning deletions mt = mt.annotate_rows(spanning_deletion=hl.any(lambda a: a == "*", mt.alleles)) # Number of Rows, Columns mt.count() # Number of Columns mt.count_cols() # Variants breakdown hl.summarize_variants(mt) # Split variants with multiple alleles into biallelic configuration. Notice that hl.count() and hl.summarize_variants() will give different numbers after multi-allele sites splitting than before mt = hl.split_multi_hts(mt) # Remove monomorphic sites mt = mt.filter_rows(mt.n_alleles > 1)
def load_icd_data(pre_phesant_data_path,
icd_codings_path,
temp_directory,
force_overwrite_intermediate: bool = False,
include_dates: bool = False,
icd9: bool = False):
"""
Load raw (pre-PHESANT) phenotype data and extract ICD codes into hail MatrixTable with booleans as entries
:param str pre_phesant_data_path: Input phenotype file
:param str icd_codings_path: Input coding metadata
:param str temp_directory: Temp bucket/directory to write intermediate file
:param bool force_overwrite_intermediate: Whether to overwrite intermediate loaded file
:param bool include_dates: Whether to also load date data (not implemented yet)
:param bool icd9: Whether to load ICD9 data
:return: MatrixTable with ICD codes
:rtype: MatrixTable
"""
if icd9:
code_locations = {'primary_codes': '41203', 'secondary_codes': '41205'}
else:
code_locations = {
'primary_codes': '41202',
'secondary_codes': '41204',
'external_codes': '41201',
'cause_of_death_codes': '40001'
}
date_locations = {'primary_codes': '41262'}
ht = hl.import_table(pre_phesant_data_path,
impute=not icd9,
min_partitions=100,
missing='',
key='userId',
types={'userId': hl.tint32})
ht = ht.checkpoint(f'{temp_directory}/pre_phesant.ht',
_read_if_exists=not force_overwrite_intermediate)
all_phenos = list(ht.row_value)
fields_to_select = {
code: [ht[x] for x in all_phenos if x.startswith(f'x{loc}')]
for code, loc in code_locations.items()
}
if include_dates:
fields_to_select.update({
f'date_{code}':
[ht[x] for x in all_phenos if x.startswith(f'x{loc}')]
for code, loc in date_locations.items()
})
ht = ht.select(**fields_to_select)
ht = ht.annotate(
**{
code: ht[code].filter(lambda x: hl.is_defined(x))
for code in code_locations
},
# **{f'date_{code}': ht[code].filter(lambda x: hl.is_defined(x)) for code in date_locations}
)
# ht = ht.annotate(primary_codes_with_date=hl.dict(hl.zip(ht.primary_codes, ht.date_primary_codes)))
all_codes = hl.sorted(
hl.array(
hl.set(
hl.flatmap(
lambda x: hl.array(x),
ht.aggregate([
hl.agg.explode(lambda c: hl.agg.collect_as_set(c),
ht[code]) for code in code_locations
],
_localize=True)))))
ht = ht.select(bool_codes=all_codes.map(lambda x: hl.struct(
**{code: ht[code].contains(x)
for code in code_locations})))
ht = ht.annotate_globals(
all_codes=all_codes.map(lambda x: hl.struct(icd_code=x)))
mt = ht._unlocalize_entries('bool_codes', 'all_codes', ['icd_code'])
mt = mt.annotate_entries(
any_codes=hl.any(lambda x: x, list(mt.entry.values())))
# mt = mt.annotate_entries(date=hl.cond(mt.primary_codes, mt.primary_codes_with_date[mt.icd_code], hl.null(hl.tstr)))
mt = mt.annotate_cols(truncated=False).annotate_globals(
code_locations=code_locations)
mt = mt.checkpoint(f'{temp_directory}/raw_icd.mt',
_read_if_exists=not force_overwrite_intermediate)
trunc_mt = mt.filter_cols((hl.len(mt.icd_code) == 3)
| (hl.len(mt.icd_code) == 4))
trunc_mt = trunc_mt.key_cols_by(icd_code=trunc_mt.icd_code[:3])
trunc_mt = trunc_mt.group_cols_by('icd_code').aggregate_entries(
**{
code: hl.agg.any(trunc_mt[code])
for code in list(code_locations.keys()) + ['any_codes']
}).aggregate_cols(n_phenos_truncated=hl.agg.count()).result()
trunc_mt = trunc_mt.filter_cols(trunc_mt.n_phenos_truncated > 1)
trunc_mt = trunc_mt.annotate_cols(
**mt.cols().drop('truncated', 'code_locations')[trunc_mt.icd_code],
truncated=True).drop('n_phenos_truncated')
mt = mt.union_cols(trunc_mt)
coding_ht = hl.read_table(icd_codings_path)
return mt.annotate_cols(**coding_ht[mt.col_key])
def annotate_variants(mt):
'''
Takes matrix table and annotates variants with gene, LOF and missense annotations by parsing VEP annotations.
:param mt: matrix table to annotate
:return: returns matrix table with new row annotations gene, LOF, and missense.
'''
try:
test = hl.is_defined(mt.row.was_split)
except Exception as e:
print('Split multi-allelics before running!')
print(e)
return
# If there is no canonical and protein-coding transcript consequence for that variant,
# give the gene corresponding to the most severe consequence.
# If there is a canonical and protein-coding transcript consequence for that variant,
# give the gene symbol associated with that transcript consequence.
canon_pc = mt.row.vep.transcript_consequences.filter(
lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'))
most_severe = mt.row.vep.transcript_consequences.filter(
lambda x: x.consequence_terms.contains(mt.row.vep.
most_severe_consequence))
mt = mt.annotate_rows(gene=hl.if_else(
hl.any(lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'),
mt.row.vep.transcript_consequences),
canon_pc.map(lambda x: x.gene_symbol),
most_severe.map(lambda x: x.gene_symbol)))
# The above returns gene symbols for all canonical and protein coding transcripts, not just the one related to the
# most severe consequence. So we will keep the above, but annotate also the gene corresponding to the most severe
# consequence as well (useful for synonymous, missense, and LOF annotations)
canon_pc = mt.row.vep.transcript_consequences.filter(
lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding')
& x.consequence_terms.contains(mt.vep.most_severe_consequence))
most_severe = mt.vep.transcript_consequences.filter(
lambda x: x.consequence_terms.contains(mt.row.vep.
most_severe_consequence))
mt = mt.annotate_rows(gene_most_severe_conseq=hl.if_else(
hl.any(lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'),
mt.vep.transcript_consequences),
canon_pc.map(lambda x: x.gene_symbol),
most_severe.map(lambda x: x.gene_symbol)))
# either if there is a canonical and protein coding transcript consequence for that variant,
# and the lof annotation is not missing and equal to HC, and the lof flag is missing or is blank,
# or if there isn't a canonical and protein coding transcript consequence for that variant and the
# transcript consequence with consequence terms containing the most severe consequence term has lof not missing,
# is equal to HC, and lof flags missing or blank,
# true, else false
canon_pc = mt.row.vep.transcript_consequences\
.filter(lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'))
most_severe = mt.row.vep.transcript_consequences\
.filter(lambda x: x.consequence_terms.contains(
mt.row.vep.most_severe_consequence))
canon_bool = (
hl.any(lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'),
mt.row.vep.transcript_consequences)
& hl.any(lambda x: hl.is_defined(x.lof), canon_pc) &
(canon_pc.map(lambda x: x.lof) == ["HC"]) &
(hl.all(lambda x: hl.is_missing(x.lof_flags) |
(x.lof_flags == ""), canon_pc)))
non_canon_bool = (~(hl.any(
lambda x: (x.canonical == 1) &
(x.biotype == 'protein_coding'), mt.row.vep.transcript_consequences))
& hl.any(lambda x: hl.is_defined(x.lof), most_severe) &
(most_severe.map(lambda x: x.lof) == ["HC"]) & (hl.all(
lambda x: hl.is_missing(x.lof_flags) |
(x.lof_flags == ""), most_severe)))
mt = mt.annotate_rows(LOF=hl.if_else(canon_bool
| non_canon_bool, True, False))
# Either if there is a canonical and protein coding transcript consequence for that variant
# whose consequence terms contain "missense variant"
# or if there is not a canonical and protein coding transcript consequence for that variant,
# but the most severe consequence is "missense variant"
# or if if there is a canonical and protein coding transcript consequence for that variant
# whose consequence terms contain "inframe deletion"
# or if there is not a canonical and protein coding transcript consequence for that variant,
# but the variant's most severe consequence is "inframe deletion"
# true else false
canon_pc = mt.row.vep.transcript_consequences\
.filter(lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'))
canon_missense_bool = canon_pc.map(lambda x: x.consequence_terms).contains(
["missense_variant"])
noncanon_missense_bool = (~(hl.any(
lambda x: (x.canonical == 1) &
(x.biotype == 'protein_coding'), mt.row.vep.transcript_consequences)) &
(mt.row.vep.most_severe_consequence
== "missense_variant"))
canon_inframe_bool = canon_pc.map(lambda x: x.consequence_terms).contains(
["inframe_deletion"])
noncanon_inframe_bool = (~(hl.any(
lambda x: (x.canonical == 1) &
(x.biotype == 'protein_coding'), mt.row.vep.transcript_consequences)) &
(mt.row.vep.most_severe_consequence
== "inframe_deletion"))
canon_inframe_ins_bool = canon_pc.map(
lambda x: x.consequence_terms).contains(["inframe_insertion"])
noncanon_inframe_ins_bool = (~(hl.any(
lambda x: (x.canonical == 1) &
(x.biotype == 'protein_coding'), mt.row.vep.transcript_consequences)) &
(mt.row.vep.most_severe_consequence
== "inframe_insertion"))
mt = mt.annotate_rows(
missense=hl.if_else((canon_missense_bool | noncanon_missense_bool
| canon_inframe_bool | noncanon_inframe_bool
| canon_inframe_ins_bool
| noncanon_inframe_ins_bool), True, False))
# If the most severe consequence is "synonymous_variant", true else false
mt = mt.annotate_rows(synonymous=hl.if_else(
mt.row.vep.most_severe_consequence == "synonymous_variant", True,
False))
# When there is a transcript consequence for that variant that is canonical,
# protein coding, and lof = "HC", its lof flags
# When there is not a transcript consequence for that variant that is canonical and protein coding,
# but there is a transcript consequence whose consequence terms contains the most severe consequence
# and its lof == HC, its lof flags
# else blank
canon_bool = hl.any(
lambda x: (x.canonical == 1) & (x.biotype == 'protein_coding'),
mt.row.vep.transcript_consequences)
canon_hc_bool = hl.any(
lambda x:
(x.canonical == 1) & (x.biotype == 'protein_coding') & (x.lof == 'HC'),
mt.row.vep.transcript_consequences)
canon_pc_hc = mt.row.vep.transcript_consequences.filter(lambda x: (
x.canonical == 1) & (x.biotype == 'protein_coding') & (x.lof == "HC"))
most_severe_bool = hl.any(
lambda x:
(x.consequence_terms.contains(mt.row.vep.most_severe_consequence)) &
(x.lof == 'HC'), mt.row.vep.transcript_consequences)
most_severe_hc = mt.row.vep.transcript_consequences.filter(lambda x: (
x.consequence_terms.contains(mt.row.vep.most_severe_consequence)) &
(x.lof == "HC"))
mt = mt.annotate_rows(LOF_flag=hl.case().when(
canon_hc_bool, canon_pc_hc.map(lambda x: x.lof_flags)).when(
~canon_bool & most_severe_bool,
most_severe_hc.map(lambda x: x.lof_flags)).default([""]))
return mt
def get_gene_intervals(gene_symbols=None, gene_ids=None, transcript_ids=None,
verbose=True, reference_genome=None, gtf_file=None):
"""Get intervals of genes or transcripts.
Get the boundaries of genes or transcripts from a GTF file, for quick filtering of a Table or MatrixTable.
On Google Cloud platform:
Gencode v19 (GRCh37) GTF available at: gs://hail-common/references/gencode/gencode.v19.annotation.gtf.bgz
Gencode v29 (GRCh38) GTF available at: gs://hail-common/references/gencode/gencode.v29.annotation.gtf.bgz
Example
-------
>>> hl.filter_intervals(ht, get_gene_intervals(gene_symbols=['PCSK9'], reference_genome='GRCh37')) # doctest: +SKIP
Parameters
----------
gene_symbols : :obj:`list` of :obj:`str`, optional
Gene symbols (e.g. PCSK9).
gene_ids : :obj:`list` of :obj:`str`, optional
Gene IDs (e.g. ENSG00000223972).
transcript_ids : :obj:`list` of :obj:`str`, optional
Transcript IDs (e.g. ENSG00000223972).
verbose : :obj:`bool`
If ``True``, print which genes and transcripts were matched in the GTF file.
reference_genome : :obj:`str` or :class:`.ReferenceGenome`, optional
Reference genome to use (passed along to import_gtf).
gtf_file : :obj:`str`
GTF file to load. If none is provided, but `reference_genome` is one of
`GRCh37` or `GRCh38`, a default will be used (on Google Cloud Platform).
Returns
-------
:obj:`list` of :class:`.Interval`
"""
GTFS = {
'GRCh37': 'gs://hail-common/references/gencode/gencode.v19.annotation.gtf.bgz',
'GRCh38': 'gs://hail-common/references/gencode/gencode.v29.annotation.gtf.bgz',
}
if reference_genome is None:
reference_genome = hl.default_reference().name
if gtf_file is None:
gtf_file = GTFS.get(reference_genome)
if gtf_file is None:
raise ValueError('get_gene_intervals requires a GTF file, or the reference genome be one of GRCh37 or GRCh38 (when on Google Cloud Platform)')
if gene_symbols is None and gene_ids is None and transcript_ids is None:
raise ValueError('get_gene_intervals requires at least one of gene_symbols, gene_ids, or transcript_ids')
ht = hl.experimental.import_gtf(gtf_file, reference_genome=reference_genome,
skip_invalid_contigs=True, min_partitions=12)
ht = ht.annotate(gene_id=ht.gene_id.split(f'\\.')[0],
transcript_id=ht.transcript_id.split('\\.')[0])
criteria = []
if gene_symbols:
criteria.append(hl.any(lambda y: (ht.feature == 'gene') & (ht.gene_name == y), gene_symbols))
if gene_ids:
criteria.append(hl.any(lambda y: (ht.feature == 'gene') & (ht.gene_id == y.split('\\.')[0]), gene_ids))
if transcript_ids:
criteria.append(hl.any(lambda y: (ht.feature == 'transcript') & (ht.transcript_id == y.split('\\.')[0]), transcript_ids))
ht = ht.filter(functools.reduce(operator.ior, criteria))
gene_info = ht.aggregate(hl.agg.collect((ht.feature, ht.gene_name, ht.gene_id, ht.transcript_id, ht.interval)))
if verbose:
info(f'get_gene_intervals found {len(gene_info)} entries:\n' +
"\n".join(map(lambda x: f'{x[0]}: {x[1]} ({x[2] if x[0] == "gene" else x[3]})', gene_info)))
intervals = list(map(lambda x: x[-1], gene_info))
return intervals
def filter_by_frequency(
t: Union[hl.MatrixTable, hl.Table],
direction: str,
frequency: float = None,
allele_count: int = None,
population: str = None,
subpop: str = None,
downsampling: int = None,
keep: bool = True,
adj: bool = True,
) -> Union[hl.MatrixTable, hl.Table]:
"""
Filter MatrixTable or Table with gnomAD-format frequency data (assumed bi-allelic/split).
gnomAD frequency data format expectation is: Array[Struct(Array[AC], Array[AF], AN, homozygote_count, meta)].
At least one of frequency or allele_count is required.
Subpop can be specified without a population if desired.
:param t: Input MatrixTable or Table
:param direction: One of "above", "below", and "equal" (how to apply the filter)
:param frequency: Frequency to filter by (one of frequency or allele_count is required)
:param allele_count: Allele count to filter by (one of frequency or allele_count is required)
:param population: Population in which to filter frequency
:param subpop: Sub-population in which to filter frequency
:param downsampling: Downsampling in which to filter frequency
:param keep: Whether to keep rows passing this frequency (passed to filter_rows)
:param adj: Whether to use adj frequency
:return: Filtered MatrixTable or Table
"""
if frequency is None and allele_count is None:
raise ValueError(
"At least one of frequency or allele_count must be specified")
if direction not in ("above", "below", "equal"):
raise ValueError(
'direction needs to be one of "above", "below", or "equal"')
group = "adj" if adj else "raw"
criteria = [lambda f: f.meta.get("group", "") == group]
if frequency is not None:
if direction == "above":
criteria.append(lambda f: f.AF[1] > frequency)
elif direction == "below":
criteria.append(lambda f: f.AF[1] < frequency)
else:
criteria.append(lambda f: f.AF[1] == frequency)
if allele_count is not None:
if direction == "above":
criteria.append(lambda f: f.AC[1] > allele_count)
elif direction == "below":
criteria.append(lambda f: f.AC[1] < allele_count)
else:
criteria.append(lambda f: f.AC[1] == allele_count)
size = 1
if population:
criteria.append(lambda f: f.meta.get("pop", "") == population)
size += 1
if subpop:
criteria.append(lambda f: f.meta.get("subpop", "") == subpop)
size += 1
# If one supplies a subpop but not a population, this will ensure this gets it right
if not population:
size += 1
if downsampling:
criteria.append(
lambda f: f.meta.get("downsampling", "") == str(downsampling))
size += 1
if not population:
size += 1
criteria.append(lambda f: f.meta.get("pop", "") == "global")
if subpop:
raise Exception(
"No downsampling data for subpopulations implemented")
criteria.append(lambda f: f.meta.size() == size)
def combine_functions(func_list, x):
cond = func_list[0](x)
for c in func_list[1:]:
cond &= c(x)
return cond
filt = lambda x: combine_functions(criteria, x)
criteria = hl.any(filt, t.freq)
return (t.filter_rows(criteria, keep=keep) if isinstance(
t, hl.MatrixTable) else t.filter(criteria, keep=keep))
def summarize_variant_filters(
t: Union[hl.MatrixTable, hl.Table],
variant_filter_field: str = "RF",
problematic_regions: List[str] = ["lcr", "segdup", "nonpar"],
single_filter_count: bool = False,
monoallelic_expr: Optional[hl.expr.BooleanExpression] = None,
extra_filter_checks: Optional[Dict[str, hl.expr.Expression]] = None,
n_rows: int = 50,
n_cols: int = 140,
) -> None:
"""
Summarize variants filtered under various conditions in input MatrixTable or Table.
Summarize counts for:
- Total number of variants
- Fraction of variants removed due to:
- Any filter
- Inbreeding coefficient filter in combination with any other filter
- AC0 filter in combination with any other filter
- `variant_filter_field` filtering in combination with any other filter in combination with any other filter
- Only inbreeding coefficient filter
- Only AC0 filter
- Only `variant_filter_field` filtering
:param t: Input MatrixTable or Table to be checked.
:param variant_filter_field: String of variant filtration used in the filters annotation on `ht` (e.g. RF, VQSR, AS_VQSR). Default is "RF".
:param problematic_regions: List of regions considered problematic to run filter check in. Default is ["lcr", "segdup", "nonpar"].
:param single_filter_count: If True, explode the Table's filter column and give a supplement total count of each filter. Default is False.
:param monoallelic_expr: Optional boolean expression of monoallelic status that logs how many monoallelic sites are in the Table.
:param extra_filter_checks: Optional dictionary containing filter condition name (key) and extra filter expressions (value) to be examined.
:param n_rows: Number of rows to display only when showing percentages of filtered variants grouped by multiple conditions. Default is 50.
:param n_cols: Number of columns to display only when showing percentages of filtered variants grouped by multiple conditions. Default is 140.
:return: None
"""
t = t.rows() if isinstance(t, hl.MatrixTable) else t
filters = t.aggregate(hl.agg.counter(t.filters))
logger.info("Variant filter counts: %s", filters)
if single_filter_count:
exp_t = t.explode(t.filters)
filters = exp_t.aggregate(hl.agg.counter(exp_t.filters))
logger.info("Exploded variant filter counts: %s", filters)
if monoallelic_expr is not None:
if isinstance(t, hl.MatrixTable):
mono_sites = t.filter_rows(monoallelic_expr).count_rows()
else:
mono_sites = t.filter(monoallelic_expr).count()
logger.info("There are %d monoallelic sites in the dataset.",
mono_sites)
filtered_expr = hl.len(t.filters) > 0
problematic_region_expr = hl.any(
lambda x: x, [t.info[region] for region in problematic_regions])
t = t.annotate(is_filtered=filtered_expr,
in_problematic_region=problematic_region_expr)
def _filter_agg_order(
t: Union[hl.MatrixTable, hl.Table],
group_exprs: Dict[str, hl.expr.Expression],
n_rows: Optional[int] = None,
n_cols: Optional[int] = None,
) -> None:
"""
Perform validity checks to measure percentages of variants filtered under different conditions.
:param t: Input MatrixTable or Table.
:param group_exprs: Dictionary of expressions to group the Table by.
:param extra_filter_checks: Optional dictionary containing filter condition name (key) and extra filter expressions (value) to be examined.
:param n_rows: Number of rows to show. Default is None (to display 10 rows).
:param n_cols: Number of columns to show. Default is None (to display 10 cols).
:return: None
"""
t = t.rows() if isinstance(t, hl.MatrixTable) else t
# NOTE: make_filters_expr_dict returns a dict with %ages of variants filtered
t.group_by(**group_exprs).aggregate(**make_filters_expr_dict(
t, extra_filter_checks, variant_filter_field)).order_by(
hl.desc("n")).show(n_rows, n_cols)
logger.info(
"Checking distributions of filtered variants amongst variant filters..."
)
_filter_agg_order(t, {"is_filtered": t.is_filtered})
logger.info(
"Checking distributions of variant type amongst variant filters...")
_filter_agg_order(t, {"allele_type": t.info.allele_type})
logger.info(
"Checking distributions of variant type and region type amongst variant filters..."
)
_filter_agg_order(
t,
{
"allele_type": t.info.allele_type,
"in_problematic_region": t.in_problematic_region,
},
n_rows,
n_cols,
)
logger.info(
"Checking distributions of variant type, region type, and number of alt alleles amongst variant filters..."
)
_filter_agg_order(
t,
{
"allele_type": t.info.allele_type,
"in_problematic_region": t.in_problematic_region,
"n_alt_alleles": t.info.n_alt_alleles,
},
n_rows,
n_cols,
)
