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JAMMA: JAX-Accelerated Mixed Model Association

Project description

CI PyPI Python 3.11+ JAX NumPy Hypothesis License: GPL-3.0

JAMMA

JAX-Accelerated Mixed Model Association — A modern Python reimplementation of GEMMA for genome-wide association studies (GWAS).

  • GEMMA-compatible: Drop-in replacement with identical CLI flags and output formats
  • Numerical equivalence: Validated against GEMMA — 100% significance agreement, 100% effect direction agreement
  • Fast: Up to 22x faster than GEMMA on kinship and 5x faster on LMM association
  • Memory-safe: Pre-flight memory checks prevent OOM crashes before allocation
  • Pure Python: JAX + NumPy stack, no C++ compilation required
  • Large-scale ready: Optional numpy-mkl ILP64 wheels (numpy 2.4.2) for >46k sample eigendecomposition

Installation

pip install jamma

Or with uv:

uv add jamma

Quick Start

# Compute kinship matrix (centered relatedness)
jamma -gk 1 -bfile data/my_study -o output

# Run LMM association (Wald test)
jamma -lmm 1 -bfile data/my_study -k output/output.cXX.txt -o results

Output files match GEMMA format exactly:

  • output.cXX.txt — Kinship matrix
  • results.assoc.txt — Association results (chr, rs, ps, n_miss, allele1, allele0, af, beta, se, logl_H1, l_remle, p_wald)
  • results.log.txt — Run log

Python API

One-call GWAS (recommended)

from jamma import gwas

# Full pipeline: load data → kinship → eigendecomp → LMM → results
result = gwas("data/my_study", kinship_file="data/kinship.cXX.txt")
print(f"Tested {result.n_snps_tested} SNPs in {result.timing['total_s']:.1f}s")

# Compute kinship from scratch and save it
result = gwas("data/my_study", save_kinship=True, output_dir="output")

# With covariates and LRT test
result = gwas("data/my_study", kinship_file="k.txt", covariate_file="covars.txt", lmm_mode=2)

# LOCO analysis (leave-one-chromosome-out)
result = gwas("data/my_study", loco=True)

# Multi-phenotype with eigendecomp reuse
result = gwas("data/my_study", write_eigen=True, phenotype_column=1)
result = gwas("data/my_study", eigenvalue_file="output/result.eigenD.txt",
              eigenvector_file="output/result.eigenU.txt", phenotype_column=2)

# SNP filtering
result = gwas("data/my_study", kinship_file="k.txt", snps_file="snps.txt", hwe=0.001)

Low-level API

from jamma.io import load_plink_binary
from jamma.kinship import compute_centered_kinship
from jamma.lmm import run_lmm_association_streaming
from jamma.lmm.eigen import eigendecompose_kinship

# Load PLINK data
data = load_plink_binary("data/my_study")

# Compute kinship
kinship = compute_centered_kinship(data.genotypes)

# Eigendecompose for LMM
eigenvalues, eigenvectors = eigendecompose_kinship(kinship)

# Run association (streaming from disk)
results = run_lmm_association_streaming(
    bed_path="data/my_study",
    phenotypes=phenotypes,
    kinship=kinship,
    chunk_size=5000,
)

Memory Safety

Unlike GEMMA, JAMMA includes pre-flight memory checks that prevent out-of-memory crashes:

from jamma.core.memory import estimate_workflow_memory

# Check memory requirements BEFORE loading data
estimate = estimate_workflow_memory(n_samples=200_000, n_snps=95_000)
print(f"Peak memory: {estimate.total_gb:.1f}GB")
print(f"Available: {estimate.available_gb:.1f}GB")
print(f"Sufficient: {estimate.sufficient}")

Key features:

  • Pre-flight checks before large allocations (eigendecomposition, genotype loading)
  • RSS memory logging at workflow boundaries
  • Incremental result writing (no memory accumulation)
  • Safe chunk size defaults with hard caps

GEMMA will silently OOM and get killed by the OS. JAMMA fails fast with clear error messages.

Performance

Benchmark on mouse_hs1940 (1,940 samples × 12,226 SNPs), Apple M3 Pro:

Operation GEMMA JAMMA Speedup
Kinship (-gk 1) 24.7s 1.1s 22.5x
LMM (-lmm 1) 27.8s 5.3s 5.2x
Total 52.5s 6.4s 8.2x

Supported Features

Current

  • Kinship matrix computation — centered (-gk 1) and standardized (-gk 2)
  • Univariate LMM Wald test (-lmm 1)
  • Likelihood ratio test (-lmm 2)
  • Score test (-lmm 3)
  • All tests mode (-lmm 4)
  • LOCO kinship — leave-one-chromosome-out analysis (-loco)
  • Eigendecomposition reuse — multi-phenotype workflows (-d/-u/-eigen)
  • Phenotype column selection (-n)
  • SNP subset selection for association and kinship (-snps/-ksnps)
  • HWE QC filtering (-hwe)
  • Pre-computed kinship input (-k)
  • Covariate support (-c)
  • PLINK binary format (.bed/.bim/.fam) with input dimension validation
  • Large-scale streaming I/O (>100k samples via numpy-mkl ILP64 — numpy 2.4.2)
  • JAX acceleration (CPU/GPU)
  • Pre-flight memory checks (fail-fast before OOM)
  • RSS memory logging at workflow boundaries
  • Incremental result writing

Planned

  • Multivariate LMM (mvLMM)

Documentation

Requirements

  • Python 3.11+
  • JAX 0.8.0+
  • NumPy 2.0+

License

GPL-3.0 (same as GEMMA)

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