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wifi-densepose/vendor/ruvector/examples/dna/benches/solver_bench.rs

314 lines
11 KiB
Rust

//! DNA Solver Benchmarks -- ruvector-solver integration
//!
//! Three benchmark groups targeting real DNA analysis scenarios:
//! A. Localized relevance via Forward Push PPR on k-mer graphs
//! B. Laplacian solve for sequence denoising/consistency
//! C. Cohort-scale label propagation
//!
//! Uses real human gene sequences from NCBI RefSeq (HBB, TP53, BRCA1, CYP2D6, INS).
use criterion::{black_box, criterion_group, criterion_main, BenchmarkId, Criterion};
use rand::rngs::StdRng;
use rand::{Rng, SeedableRng};
use ruvector_solver::cg::ConjugateGradientSolver;
use ruvector_solver::forward_push::ForwardPushSolver;
use ruvector_solver::neumann::NeumannSolver;
use ruvector_solver::traits::SolverEngine;
use ruvector_solver::types::{ComputeBudget, CsrMatrix};
use rvdna::kmer_pagerank::KmerGraphRanker;
use rvdna::real_data;
// ============================================================================
// Helpers
// ============================================================================
/// Real gene sequences from NCBI RefSeq
fn real_gene_sequences() -> Vec<&'static [u8]> {
vec![
real_data::HBB_CODING_SEQUENCE.as_bytes(),
real_data::TP53_EXONS_5_8.as_bytes(),
real_data::BRCA1_EXON11_FRAGMENT.as_bytes(),
real_data::CYP2D6_CODING.as_bytes(),
real_data::INS_CODING.as_bytes(),
]
}
/// Generate synthetic DNA sequences with mutations from a template
fn mutated_sequences(template: &[u8], count: usize, mutation_rate: f64, seed: u64) -> Vec<Vec<u8>> {
let mut rng = StdRng::seed_from_u64(seed);
let bases = [b'A', b'C', b'G', b'T'];
(0..count)
.map(|_| {
template
.iter()
.map(|&b| {
if rng.gen::<f64>() < mutation_rate {
bases[rng.gen_range(0..4)]
} else {
b
}
})
.collect()
})
.collect()
}
/// Build k-mer fingerprint vector for a sequence using FNV-1a hashing
fn fingerprint(seq: &[u8], k: usize, dims: usize) -> Vec<f64> {
if seq.len() < k {
return vec![0.0; dims];
}
let mut counts = vec![0u32; dims];
for window in seq.windows(k) {
let hash = fnv1a(window);
counts[hash % dims] += 1;
}
let total: u32 = counts.iter().sum();
if total == 0 {
return vec![0.0; dims];
}
let inv = 1.0 / total as f64;
counts.iter().map(|&c| c as f64 * inv).collect()
}
fn fnv1a(data: &[u8]) -> usize {
let mut hash: u64 = 14695981039346656037;
for &byte in data {
hash ^= byte as u64;
hash = hash.wrapping_mul(1099511628211);
}
hash as usize
}
fn cosine_sim(a: &[f64], b: &[f64]) -> f64 {
let dot: f64 = a.iter().zip(b).map(|(x, y)| x * y).sum();
let na: f64 = a.iter().map(|x| x * x).sum::<f64>().sqrt();
let nb: f64 = b.iter().map(|x| x * x).sum::<f64>().sqrt();
if na < 1e-15 || nb < 1e-15 {
0.0
} else {
dot / (na * nb)
}
}
/// Build a column-stochastic transition matrix from sequence fingerprints.
///
/// Edge weights are cosine similarities above `threshold`, normalized so
/// each column sums to 1. Isolated nodes get a self-loop.
fn build_stochastic_matrix(fps: &[Vec<f64>], threshold: f64) -> CsrMatrix<f64> {
let n = fps.len();
let mut col_sums = vec![0.0f64; n];
let mut entries: Vec<(usize, usize, f64)> = Vec::new();
for i in 0..n {
for j in 0..n {
if i == j {
continue;
}
let sim = cosine_sim(&fps[i], &fps[j]);
if sim > threshold {
entries.push((i, j, sim));
col_sums[j] += sim;
}
}
}
let mut normalized: Vec<(usize, usize, f64)> = entries
.into_iter()
.map(|(i, j, w)| (i, j, w / col_sums[j].max(1e-15)))
.collect();
// Self-loops for dangling nodes
for j in 0..n {
if col_sums[j] < 1e-15 {
normalized.push((j, j, 1.0));
}
}
CsrMatrix::<f64>::from_coo(n, n, normalized)
}
/// Build graph Laplacian from fingerprints: L = D - A (with small regularization).
///
/// The regularization term (0.01 added to each diagonal) ensures the Laplacian
/// is strictly positive definite, which is required for both the Neumann solver
/// (diagonal dominance) and the CG solver (SPD requirement).
fn build_laplacian(fps: &[Vec<f64>], threshold: f64) -> CsrMatrix<f64> {
let n = fps.len();
let mut degree = vec![0.0f64; n];
let mut entries: Vec<(usize, usize, f64)> = Vec::new();
for i in 0..n {
for j in (i + 1)..n {
let sim = cosine_sim(&fps[i], &fps[j]);
if sim > threshold {
entries.push((i, j, -sim));
entries.push((j, i, -sim));
degree[i] += sim;
degree[j] += sim;
}
}
}
// Diagonal: degree + regularization for positive-definiteness
for (i, &d) in degree.iter().enumerate() {
entries.push((i, i, d + 0.01));
}
CsrMatrix::<f64>::from_coo(n, n, entries)
}
// ============================================================================
// Group A: Localized Relevance on K-mer Graphs (Forward Push PPR)
// ============================================================================
fn localized_relevance_benchmarks(c: &mut Criterion) {
let mut group = c.benchmark_group("solver_ppr");
group.sample_size(30);
// Benchmark with real genes using KmerGraphRanker
{
let genes = real_gene_sequences();
let ranker = KmerGraphRanker::new(11, 128);
group.bench_function("real_genes_5seq", |b| {
b.iter(|| black_box(ranker.rank_sequences(&genes, 0.15, 1e-4, 0.05)));
});
}
// Scale with mutated cohorts using ForwardPushSolver directly
for &n in &[50usize, 100, 500] {
let template = real_data::HBB_CODING_SEQUENCE.as_bytes();
let mutated = mutated_sequences(template, n, 0.05, 42);
let fps: Vec<Vec<f64>> = mutated.iter().map(|s| fingerprint(s, 11, 128)).collect();
let matrix = build_stochastic_matrix(&fps, 0.05);
let solver = ForwardPushSolver::new(0.15, 1e-4);
group.bench_with_input(BenchmarkId::new("ppr_single_source", n), &n, |b, _| {
b.iter(|| black_box(solver.ppr_from_source(&matrix, 0)));
});
}
group.finish();
}
// ============================================================================
// Group B: Laplacian Solve for Denoising / Consistency
// ============================================================================
fn laplacian_solve_benchmarks(c: &mut Criterion) {
let mut group = c.benchmark_group("solver_laplacian");
group.sample_size(20);
for &n in &[50usize, 100, 500] {
let template = real_data::TP53_EXONS_5_8.as_bytes();
let mutated = mutated_sequences(template, n, 0.03, 42);
let fps: Vec<Vec<f64>> = mutated.iter().map(|s| fingerprint(s, 11, 128)).collect();
let laplacian = build_laplacian(&fps, 0.1);
// RHS: noisy signal (first 10% = 1.0, rest = small noise)
let mut rhs = vec![0.0f64; n];
let mut rng = StdRng::seed_from_u64(42);
for i in 0..n {
rhs[i] = if i < n / 10 {
1.0
} else {
rng.gen::<f64>() * 0.1
};
}
let budget = ComputeBudget::default();
// Neumann solver (via SolverEngine trait, f64 -> f32 conversion)
let neumann = NeumannSolver::new(1e-6, 200);
group.bench_with_input(BenchmarkId::new("neumann_denoise", n), &n, |b, _| {
b.iter(|| {
// Neumann may fail on non-diag-dominant Laplacians;
// the benchmark measures attempt latency regardless.
let _ = black_box(SolverEngine::solve(&neumann, &laplacian, &rhs, &budget));
});
});
// CG solver (preconditioned, well-suited for SPD Laplacians)
let cg = ConjugateGradientSolver::new(1e-6, 500, true);
group.bench_with_input(BenchmarkId::new("cg_denoise", n), &n, |b, _| {
b.iter(|| black_box(SolverEngine::solve(&cg, &laplacian, &rhs, &budget)));
});
}
group.finish();
}
// ============================================================================
// Group C: Cohort-Scale Label Propagation
// ============================================================================
fn cohort_propagation_benchmarks(c: &mut Criterion) {
let mut group = c.benchmark_group("solver_cohort");
group.sample_size(10);
for &n in &[100usize, 500, 1000] {
// Build mixed cohort: HBB variants + TP53 variants + BRCA1 variants
let mut all_seqs: Vec<Vec<u8>> = Vec::new();
let genes: Vec<&[u8]> = vec![
real_data::HBB_CODING_SEQUENCE.as_bytes(),
real_data::TP53_EXONS_5_8.as_bytes(),
real_data::BRCA1_EXON11_FRAGMENT.as_bytes(),
];
let per_gene = n / 3;
for (gi, gene) in genes.iter().enumerate() {
let variants = mutated_sequences(gene, per_gene, 0.04, 42 + gi as u64);
all_seqs.extend(variants);
}
// Fill remainder with HBB variants
while all_seqs.len() < n {
let extra = mutated_sequences(genes[0], 1, 0.05, 99 + all_seqs.len() as u64);
all_seqs.extend(extra);
}
all_seqs.truncate(n);
let fps: Vec<Vec<f64>> = all_seqs.iter().map(|s| fingerprint(s, 11, 128)).collect();
let laplacian = build_laplacian(&fps, 0.05);
// Label propagation: known labels for first 10% of each gene group
let mut labels = vec![0.0f64; n];
let labeled_count = (per_gene / 10).max(1);
for i in 0..labeled_count.min(n) {
labels[i] = 1.0; // Gene group 1 (HBB)
}
for i in per_gene..(per_gene + labeled_count).min(n) {
labels[i] = 2.0; // Gene group 2 (TP53)
}
let start_3 = 2 * per_gene;
for i in start_3..(start_3 + labeled_count).min(n) {
labels[i] = 3.0; // Gene group 3 (BRCA1)
}
let cg = ConjugateGradientSolver::new(1e-6, 1000, true);
let budget = ComputeBudget::default();
group.bench_with_input(BenchmarkId::new("label_propagation", n), &n, |b, _| {
b.iter(|| black_box(SolverEngine::solve(&cg, &laplacian, &labels, &budget)));
});
}
group.finish();
}
// ============================================================================
// Configuration
// ============================================================================
criterion_group!(
benches,
localized_relevance_benchmarks,
laplacian_solve_benchmarks,
cohort_propagation_benchmarks,
);
criterion_main!(benches);