v0.57.41 · desktop app · macOS & Windows

One platform for HLA, KIR & LILR immunogenetics.

TRIAD is a validated, local-first analysis platform for case-control association and population genetics across the three gene systems that drive innate and adaptive immune variation — no assembling separate tools, no data leaving your machine.

21 methods, independently validated Tested to 100,000 samples Runs entirely on your machine
HLA KIR LILR
CASE-CONTROL · POPULATION GENETICS · FUNCTIONAL INTERACTION
What it does

Two study designs, one genotype table.

A typical immunogenetic study touches allele frequencies, association testing, amino-acid analysis, haplotypes, and diversity statistics — usually across several separately-validated tools, with data reformatted by hand at every handoff. TRIAD imports one standardized table and runs either track, or both, without switching tools.

CASE–CONTROL

Association testing

Find and quantify disease associations, allele- and amino-acid-level.

  • Allele & carrier-model association
  • Amino-acid association (BIGDAWG-style)
  • Haplotype association
  • Meta-analysis (fixed & random effects)
  • HED (heterozygosity/divergence) scoring
POPULATION GENETICS

Descriptive & structural analysis

Characterize a cohort or compare populations in depth.

  • Allele & haplotype frequencies (EM)
  • Linkage disequilibrium (D′, Wn, ALD)
  • Hardy-Weinberg equilibrium
  • Fst / AMOVA, gene diversity
  • Phylogeny (NJ / UPGMA)
DIFFERENTIATOR

Functional interactions

The analysis most tools don't offer at all.

  • HLA–KIR receptor–ligand pairing
  • Missing-ligand analysis
  • HLA–LILR & KIR–LILR (LRC) linkage
  • KIR / LILR genotype & CNV calling
  • Gene-content carrier association

HLA, KIR, and LILR, analyzed together, not adjacently. Most tools handle one gene system well. TRIAD's functional-interaction layer treats receptor–ligand relationships across all three as first-class analyses, not a manual cross-reference step at the end.

Why trust it

Every method checked against an external reference.

Not "tested" in the informal sense — each analysis is reproduced against a named gold standard (BIGDAWG, Arlequin, statsmodels, or the primary literature) and the concordance is recorded, re-runnable from the repository's validation/ suite.

21
methods independently validated
100k
samples, no crash or failure
MethodReference / gold standardConcordance
Allele frequenciesBIGDAWG (Pappas 2016)exact, max diff 0
Case-control associationBIGDAWG (Pappas 2016)OR exact
Hardy-Weinberg equilibriumBIGDAWG (Pappas 2016)exact (χ², dof, p)
AMOVA / FstArlequin 3.5.2.2exact vs. Arlequin
HED (class I)Pierini & Lenz (2018)exact to 1e-9
Show all 21 validated methods
Amino-acid associationBIGDAWG (Pappas 2016)omnibus χ² exact
Conditional amino-acidstatsmodels (logistic LRT)match to ~1e-4
EM haplotype frequenciesExcoffier & Slatkin (1995)known-answer, max err ~5e-3
Haplotype associationscipy Fisher + BIGDAWG (OR)Fisher exact match
Gene diversity & heterozygosityArlequin 3.5.2.2 / Nei (1987)exact vs. Arlequin
Ewens-Watterson neutralityEwens (1972) / Slatkin (1996)reproduces analytic moments
Linkage disequilibrium (D′, Wn, ALD)Hedrick (1987) / Thomson-Single (2014)matches worked example, 7 dp
Logistic regression (Wald)statsmodelsmatch to ~1e-6
Logistic regression (Firth)independent penalised-likelihood optimisermatch to ~1e-8
Meta-analysis (DerSimonian-Laird)statsmodels (DL)match to ~1e-4
Meta-analysis (Mantel-Haenszel)Robins-Breslow-Greenland (1986)OR + variance exact
Functional KIR-ligand pairingImmunogenetics literaturematches published rules
Phylogeny (NJ / UPGMA)Biopython DistanceTreeConstructorexact topology match
KIR / LILR gene-content associationscipy Fisher + BIGDAWGFisher exact
HED (class II)no external gold standardinternal logic verified

Full methodology and reproduction scripts live in the repository's validation/ suite.

See it, not just read about it

Load, analyze, report.

The three-step workflow TRIAD is built around, shown on the bundled demo cohort.

TRIAD data grid after loading the demo cohort, showing 160 samples typed across HLA, KIR, and LILR
01 Load
TRIAD case-control association results table for the demo cohort
02 Analyze
Generated TRIAD case-control association report, PDF output
03 Report
TRIAD haplotype linkage Sankey diagram across A, C, B, DRB1, DQA1, DQB1, DPA1, DPB1
04 Haplotype linkage — depth beyond allele counts
Real TRIAD meta-analysis forest plot for HLA-C*06:02 across three cohorts, fixed and random effects
05 Meta-analysis — pooled across cohorts C*06:02 · demo_meta_3centre_stratified · TRIAD v0.57.41

Your genotype data never leaves your machine.

TRIAD is a desktop application, not a web upload service. Analysis runs locally, which matters for patient-derived data and sidesteps the data-governance questions a cloud tool would raise.

Get TRIAD

Request access.

TRIAD isn't publicly listed yet — the repository is private ahead of publication. Tell us a little about yourself and confirm your email, and you'll be taken straight to the download page.

You'll get a confirmation email — click the link there to verify your address, and it will take you directly to the download page. That page isn't linked anywhere else on the site.