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bio-vcf-statistics

使用bcftools stats和gtcheck生成变异统计信息、样本一致性以及质量指标。在评估变异质量、比较样本或汇总VCF内容时使用。

person作者: jakexiaohubgithub
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Version Compatibility

Reference examples tested with: bcftools 1.19+, vcftools 0.1.16+, somalier 0.2.19+, peddy 0.4.8+, cyvcf2 0.30+, numpy 1.26+

Before using code patterns, verify installed versions match. If versions differ:

  • Python: pip show <package> then help(module.function) to check signatures
  • CLI: <tool> --version then <tool> --help to confirm flags

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Note: bcftools gtcheck was rewritten around bcftools 1.10; the old -G/--GTs-only flag is gone. Modern gtcheck cross-checks all samples in one file when -g is omitted, and uses -E/--error-probability. Verify flags against the installed build.

VCF Statistics

"Is this callset any good, and are the samples who the manifest says they are?" -> Summarize variant counts and quality distributions, then read each QC metric as a signal whose expected value is context-dependent.

  • CLI: bcftools stats (+ plot-vcfstats), vcftools, somalier, peddy
  • Python: cyvcf2 for custom per-record statistics

The governing principle

No QC metric has a universal pass value. Each metric's expected range depends on the assay (WGS vs WES), the sample's ancestry, and the cohort it sits in, so QC is not threshold-checking but reading a deviation for its mechanistic meaning and acting on it. Three rules follow. First, always compare a sample against a matched cohort (same assay, same inferred ancestry), never against an absolute number. Second, order of operations matters: apply genotype-level filters (set ./. where GQ/DP/allele-balance fail) BEFORE computing cohort missingness, call rate, or HWE, because low-quality genotypes left in the matrix drive spurious missingness and HWE deviation. Third, sample-identity QC is a graph problem, not a per-sample check: build the all-pairs relatedness matrix and reconcile it against the declared pedigree/manifest, and do this BEFORE any association or burden analysis, because one undetected swap or contaminated sample can fabricate or erase a genome-wide-significant hit.

QC metric decision table

Expected values are stated conventions (they shift with capture kit, ancestry, reference build, and caller); treat them as starting points and confirm against a matched cohort.

| Metric | Expected (WGS) | Expected (WES) | A deviation MEANS | Action | |--------|---------------|---------------|-------------------|--------| | Ti/Tv (overall) | ~2.0-2.1 | ~3.0-3.3 | Low -> false-positive transversions dilute the signal (random errors have Ti/Tv ~0.5); high -> over-filtering removed transversions | Tighten site filters if low; check filter for transversion bias if high | | Ti/Tv (novel only) | near overall | near overall | Novel Ti/Tv well below the known-site value -> FP contamination in the novel fraction | Raise stringency; the novel set is where FPs concentrate | | Het/hom ratio | ancestry-dependent (~1.5-1.6 EUR, ~2.0+ AFR) | same | High vs same-ancestry cohort -> contamination or reference bias; low -> inbreeding/consanguinity/ROH or chromosome loss | Stratify by ancestry first; then flag within-ancestry outliers | | Novel fraction (vs dbSNP) | low for common; high for rare/singleton | same | Novel COMMON variants -> almost always artifacts; high novel rare -> expected or under-studied population | Stratify novel% by frequency; investigate common novels | | Call rate (per sample) | >95-98% | >95-98% | Low -> low-coverage/low-quality sample | Drop worst samples, then recompute per-variant missingness (iterate) | | Call rate (per variant) | >95-99% | >95-99% | Low -> site in a hard-to-genotype region | Drop worst variants after sample QC; rare variants tolerate more missing | | Het allele-balance (hets) | centered on 0.5 | 0.5 | Shifted away from 0.5 + elevated het count -> contamination signature | Confirm with VerifyBamID2 (on the BAM) or CHARR (on the VCF/gVCF) -- the real test | | Excess-het / HWE | in equilibrium within ancestry | same | EXCESS het -> collapsed paralog/CNV mapping artifact; het DEFICIT -> often real (Wahlund/inbreeding) | Filter on excess het only, within ancestry, in controls; do NOT blanket-filter HWE | | Relatedness (kinship) | matches manifest | matches manifest | Unexpected high kinship -> sample swap/duplicate; a "replicate" that is not -> mislabel | Reconcile the all-pairs matrix against the pedigree with KING/somalier/peddy |

bcftools stats

Goal: Generate comprehensive variant statistics (counts, Ti/Tv, per-sample het/hom and singletons, indel and depth distributions).

Approach: Run bcftools stats and read the section-tagged output lines; add -s - for per-sample metrics.

bcftools stats input.vcf.gz > stats.txt              # cohort-level
bcftools stats -s - input.vcf.gz > per_sample.txt    # per-sample (PSC/PSI lines)
bcftools stats file1.vcf.gz file2.vcf.gz > cmp.txt   # compare two callsets
plot-vcfstats -p qc_plots/ stats.txt                 # render PDF + PNGs (needs matplotlib)

Output sections: SN summary numbers, TSTV transition/transversion, SiS singletons, AF allele-frequency spectrum, QUAL quality distribution, IDD indel-length distribution, ST substitution types, DP depth distribution, PSC per-sample counts (hom-ref, het, hom-alt, transitions, transversions, missing), PSI per-sample indels.

bcftools stats input.vcf.gz | grep "^SN"    | cut -f3-   # counts
bcftools stats input.vcf.gz | grep "^TSTV"  | cut -f5     # Ti/Tv ratio
bcftools stats -s - input.vcf.gz | grep "^PSC"           # per-sample het/hom/missing

Ti/Tv ratio

Transitions (purine<->purine A<->G, pyrimidine<->pyrimidine C<->T) are favored over transversions because CpG deamination (methylated C->T) is the single most common vertebrate point mutation and is a transition, and because transitions are more often synonymous. A random error spectrum gives Ti/Tv ~0.5, so a callset diluted with false positives drifts DOWNWARD. WES runs higher than WGS (~3.0-3.3 vs ~2.0-2.1) because coding regions are CpG- and constraint-enriched and transitions at CpGs plus codon degeneracy push the ratio up.

Ti/Tv is the single fastest gross-error smell test. A WES callset reporting Ti/Tv ~2.1 is telling the analyst the filtering is too loose. Stratify: compute Ti/Tv on the novel fraction separately (below) since that is where false positives concentrate. Ancestry and target design shift the exact number, so compare against a matched cohort, not the absolute.

Het/hom ratio and ancestry

The per-sample het:non-ref-hom ratio reflects heterozygosity relative to the reference, so it is strongly ancestry-dependent: African-ancestry genomes diverge more from GRCh (a mostly European-ancestry assembly) and carry more het calls (commonly ~2.0+), European ancestry sits ~1.5-1.6, and the value shifts across populations. A single global het/hom cutoff is therefore wrong: it would flag every AFR sample in a EUR-tuned pipeline.

Infer ancestry first (peddy/somalier project onto 1000 Genomes PCs), then flag outliers WITHIN each ancestry group. An elevated het/hom versus same-ancestry peers indicates contamination (foreign reads manufacture spurious hets) or reference bias; a depressed het/hom indicates inbreeding/consanguinity, a long run of homozygosity, or chromosome loss.

Novel/known ratio via dbSNP

Overlapping the callset with dbSNP gives an orthogonal false-positive signal independent of Ti/Tv. Annotate known/novel and stratify by frequency, because the diagnostic differs by allele frequency: novel COMMON variants are almost always artifacts (real common variants are already catalogued), while novel rare/singleton variants are expected and biologically real. A single novel% without frequency stratification is uninformative.

bcftools annotate -a dbsnp.vcf.gz -c ID input.vcf.gz -Oz -o annotated.vcf.gz
# novel fraction = records with ID "." over total; stratify by INFO/AF
bcftools view -H annotated.vcf.gz | awk '{n++; if($3==".") novel++} END{print "novel:", novel/n}'

Missingness and call rate

Call rate is the fraction of sites with a non-missing genotype for a sample; missingness is its complement. Only ./. (no-call) counts as missing; 0/0 (confident hom-ref) does NOT, so treating no-call as hom-ref biases allele frequencies. GWAS convention drops samples below ~95-98% call rate and variants below ~95-99% (dataset-dependent conventions).

The iteration trap: sample-level and variant-level missingness are coupled, so applying both thresholds in one pass is wrong. Drop the worst samples, recompute per-variant missingness, drop the worst variants, and repeat. Critically, apply genotype-level filters (./. where GQ<20 or DP<8) BEFORE computing cohort missingness or HWE, or low-quality genotypes will drive both.

vcftools --gzvcf input.vcf.gz --missing-indv --out sample_miss   # .imiss (per-sample)
vcftools --gzvcf input.vcf.gz --missing-site --out site_miss     # .lmiss (per-site)

HWE filtering (excess-het only)

Hardy-Weinberg testing flags genotype frequencies that deviate from p^2:2pq:q^2, but a naive two-sided HWE gate throws away real biology. The discipline:

  • Filter on EXCESS heterozygosity only. Heterozygote excess is the signature of a mapping artifact: a duplicated/collapsed region piles reads from two paralogous copies onto one locus, manufacturing spurious hets everywhere. Heterozygote DEFICIT, by contrast, is often real (Wahlund effect from substructure, inbreeding, selection, a true null allele). GATK's ExcessHet and InbreedingCoeff and gnomAD's ExcessHet filter the excess side only.
  • Compute within an ancestry-homogeneous subgroup. Pooling populations with different allele frequencies induces a Wahlund het-deficit that mimics genotyping error; HWE on a mixed cohort filters good variants.
  • Use the EXACT test, not chi-square. The chi-square approximation is anticonservative for rare variants and small samples; the standard is the Wigginton-Cutler-Abecasis exact test (implemented in vcftools --hardy and PLINK).
  • In case/control studies, compute HWE in CONTROLS only. A true association at a strong-effect locus produces HWE deviation in cases; filtering it removes the hit.
vcftools --gzvcf controls.vcf.gz --hardy --out hwe               # exact-test P per site
# GATK ExcessHet (phred): larger = more excess het = more suspect
bcftools query -f '%CHROM\t%POS\t%INFO/ExcessHet\n' input.vcf.gz | awk '$3>54.69'

The threshold 54.69 is GATK's default ExcessHet cutoff (phred-scaled p ~= 3.4e-6, ~the 1000-sample z=-4.5 boundary); tune it to the cohort size.

Contamination signatures

Cross-sample contamination is visible in VCF statistics before any dedicated test: the het allele-balance distribution shifts away from 0.5 (foreign reads add minor-allele support at true hom sites and skew true hets), the het count and het/hom ratio rise, and the novel-fraction Ti/Tv drops. These are SIGNALS, not the measurement. The real test runs on the BAM/CRAM: VerifyBamID2 (Zhang et al. 2020) estimates the contamination fraction alpha ancestry-agnostically by modeling observed allele fractions against population frequencies, and CHARR estimates alpha directly from VCF-level reference-read counts at hom-alt sites. An alpha above ~0.02-0.03 is a red flag; somatic pipelines are sensitive to even 1%. GATK pipelines feed --contamination alpha from VerifyBamID2. See variant-calling/gatk-variant-calling for wiring contamination estimates into calling.

# quick het allele-balance sanity check from AD (het genotypes only)
bcftools query -i 'GT="het"' -f '[%AD]\n' input.vcf.gz | \
    awk -F',' '{ab=$2/($1+$2); s+=ab; n++} END{print "mean het AB:", s/n}'   # expect ~0.5

Sample-swap, relatedness, and sex checks (mandatory cohort QC)

Sample swaps are among the most common errors in sequencing studies, so identity QC is not optional. Build the all-pairs relatedness matrix and reconcile it against the manifest; swaps appear as off-diagonal surprises (unexpected relatedness) or on-diagonal failures (a "replicate" that is not).

| Tool | Input | Detects | Notes | |------|-------|---------|-------| | bcftools gtcheck | VCF | Same-file swaps/duplicates (quick) | Native, no reference panel; discordance score, not a relatedness graph | | KING (Manichaikul 2010) | PLINK bed | Robust kinship without allele-freq/ancestry assumptions | Reference method; kinship bands below | | peddy (Pedersen 2017) | VCF + PED | Reported vs inferred sex, relationships, ancestry (PCA on 1000G) | Fast, VCF-only; ideal PED-vs-VCF reconciliation | | somalier (Pedersen 2020) | BAM/CRAM/VCF | Relatedness/ancestry/sex at scale; cross-checks RNA-seq vs WGS | Tiny per-sample sketches; tens of thousands of samples in seconds |

KING kinship coefficient bands: >0.354 duplicate/MZ twin, [0.177, 0.354] first-degree (parent-child, full sib), [0.0884, 0.177] second-degree, [0.0442, 0.0884] third-degree. A pair not expected to be related at ~0.5 is a swap or duplicate.

# bcftools: cross-check all samples in one file (no -g), or against a truth VCF (-g)
bcftools gtcheck input.vcf.gz > gtcheck.txt          # DC lines: query, genotyped, discordance, sites
bcftools gtcheck -g reference.vcf.gz query.vcf.gz    # concordance to a genotyping panel

# peddy: PED-vs-VCF sex/relatedness/ancestry, 4 CPUs, HTML + CSVs
python -m peddy -p 4 --plot --prefix cohort_qc input.vcf.gz cohort.ped

# somalier: extract sketches then relate against the pedigree
somalier extract -d extracted/ --sites sites.vcf.gz -f ref.fa input.vcf.gz
somalier relate --ped cohort.ped extracted/*.somalier    # writes an HTML relatedness report
somalier ancestry --labels 1kg-labels.tsv 1kg/*.somalier ++ extracted/*.somalier    # PCA projection (labelled ++ query)

# vcftools: KING-robust kinship directly from a VCF
vcftools --gzvcf input.vcf.gz --relatedness2 --out kin    # .relatedness2 (Manichaikul method)

Stratified evaluation

A caller with 99% overall accuracy may drop to 70% in difficult regions, so single-number accuracy hides where a callset fails. Evaluate stratified by region class using GIAB stratification BED files (github.com/genome-in-a-bottle/genome-stratifications).

bcftools stats -R easy_regions.bed      input.vcf.gz > easy.txt
bcftools stats -R difficult_regions.bed input.vcf.gz > difficult.txt

Key strata and their failure modes: homopolymer runs (systematic indel errors, Illumina/Ion Torrent), tandem repeats / low-complexity (alignment ambiguity inflates FP and FN), segmental duplications (paralogous mapping -> false hets), high-GC >70% / low-GC <25% (coverage-bias missingness), MHC/centromeric (extreme polymorphism or repetitiveness). A drop in Ti/Tv within difficult regions confirms elevated false positives there.

Quick counts with query

bcftools view -H input.vcf.gz | wc -l              # total records
bcftools view -v snps   -H input.vcf.gz | wc -l    # SNPs
bcftools view -v indels -H input.vcf.gz | wc -l    # indels
bcftools view -f PASS   -H input.vcf.gz | wc -l    # PASS variants
bcftools query -f '%QUAL\n' input.vcf.gz | awk '{s+=$1;n++} END{print "mean QUAL:", s/n}'

See examples/vcf_stats.py for a cyvcf2 script computing counts, Ti/Tv, and mean QUAL in one pass; the usage guide covers per-sample genotype distributions and the allele-frequency spectrum.

Quick Reference

| Task | Command | |------|---------| | Full stats | bcftools stats input.vcf.gz | | Per-sample het/hom/missing | bcftools stats -s - input.vcf.gz \| grep "^PSC" | | Ti/Tv ratio | bcftools stats input.vcf.gz \| grep "^TSTV" \| cut -f5 | | Per-sample missingness | vcftools --gzvcf in.vcf.gz --missing-indv | | Exact HWE (controls) | vcftools --gzvcf controls.vcf.gz --hardy | | KING kinship | vcftools --gzvcf in.vcf.gz --relatedness2 | | Sex/ancestry/relatedness | python -m peddy -p 4 --plot --prefix qc in.vcf.gz in.ped | | Scalable identity QC | somalier extract ... then somalier relate --ped ... | | Plot stats | plot-vcfstats -p dir stats.txt |

Common Errors

| Symptom | Cause | Fix | |---------|-------|-----| | Every AFR sample flagged as high het/hom | Single global cutoff across ancestries | Infer ancestry, flag outliers within each group | | Good variants filtered by HWE | Two-sided HWE on a mixed cohort or on cases | Excess-het only, within ancestry, controls-only | | Spurious HWE/missingness | Cohort metrics computed before genotype filtering | Set ./. on low GQ/DP first, then recompute | | bcftools gtcheck -G 1 errors | -G removed after the 1.10 rewrite | Drop -G; cross-check runs by default without -g | | Low Ti/Tv only in novel set | False positives concentrate in novel variants | Raise stringency; recheck against dbSNP overlap | | plot-vcfstats not found / no plots | matplotlib missing or not on PATH | pip install matplotlib; check which plot-vcfstats |

Related Skills

  • variant-calling/filtering-best-practices - Apply the site and genotype filters these metrics motivate
  • variant-calling/gatk-variant-calling - VerifyBamID2 contamination estimate feeding --contamination
  • variant-calling/variant-normalization - Normalize before comparing or annotating call sets
  • variant-calling/vcf-basics - View, query, and understand VCF fields
  • variant-calling/vcf-manipulation - Compare and merge call sets
  • variant-calling/joint-calling - Cohort genotyping where population QC applies
  • alignment-files/bam-statistics - Upstream alignment QC that drives variant statistics

References

  • Danecek P, Bonfield JK, Liddle J, et al. Twelve years of SAMtools and BCFtools. 2021 GigaScience 10:giab008. (bcftools stats/gtcheck)
  • Danecek P, Auton A, Abecasis G, et al. The variant call format and VCFtools. 2011 Bioinformatics 27:2156-2158. (vcftools QC)
  • Wigginton JE, Cutler DJ, Abecasis GR. A note on exact tests of Hardy-Weinberg equilibrium. 2005 American Journal of Human Genetics 76:887-893. (exact HWE test)
  • Manichaikul A, Mychaleckyj JC, Rich SS, et al. Robust relationship inference in genome-wide association studies. 2010 Bioinformatics 26:2867-2873. (KING kinship)
  • Pedersen BS, Quinlan AR. Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. 2017 American Journal of Human Genetics 100:406-413. (peddy)
  • Pedersen BS, Bhetariya PJ, Brown J, et al. Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches. 2020 Genome Medicine 12:62. (somalier)
  • Zhang F, Flickinger M, Gagliano Taliun SA, et al. Ancestry-agnostic estimation of DNA sample contamination from sequence reads. 2020 Genome Research 30:185-194. (VerifyBamID2)