Fast calculation of approximately independent LD blocks
Project description
LDetect-lite
A modern, fast re-implementation of LDetect, a method for calculating approximately independent linkage disequilibrium (LD) blocks in the human genome. The algorithm is described in Berisa & Pickrell, 2016.
Installation
Install from PyPI via:
pip install ldetect-lite
Or, with uv:
uv add ldetect-lite
This installs three equivalent CLI entry points — ldetect-lite, ldetect, and ldl — so pick whichever is most convenient; examples below use ldetect.
The main ldetect run pipeline also requires htslib. Specifically, tabix is used to stream VCF files to ldetect calc-covariance, and so must be on PATH.
Optional (--generate-heatmap): install matplotlib with pip install "ldetect-lite[heatmap]", or use uv sync --extra heatmap from a source checkout. Generating covariance heatmaps requires a matplotlib install.
Development
Install from source
git clone https://github.com/adamyhe/ldetect-lite.git
cd ldetect-lite
uv sync --extra dev
From a development checkout, run CLI commands through uv run so they use the managed environment.
Usage
End-to-end pipeline
uv run ldetect run \
--genetic-map chr2.interpolated_genetic_map.gz \
--reference-panel 1000G.chr2.vcf.gz \
--individuals eurinds.txt \
--chromosome chr2 \
--output-dir results/chr2/
This writes results/chr2/chr2-ld-blocks.bed — a BED file of approximately independent LD blocks.
Global options (before the subcommand):
-v / --verbosity {debug,info,warning,error}— logging verbosity (default:info; usewarningto silence progress messages,debugfor full detail)
Options:
--ne FLOAT— effective population size Ne used by the Wen & Stephens shrinkage estimator (default: 11418.0, the CEU/HapMap II value; reproduction configs may override this for non-European populations)--cov-cutoff FLOAT— LD pairs with absolute shrinkage correlation below this threshold are not written to disk, reducing storage (default: 1e-7)--covariance-cache {compact,full}— partition cache schema forldetect run(default:compact). Compact caches write only canonical position pairs,shrink_ld, diagonals, and lookup indexes, which is enough for restartable matrix-to-vector, metric, and local-search steps. Usefullwhen debugging or when later running full-matrix/heatmap readers.--covariance-compression {lzf,zstd}— HDF5 compression codec for covariance partitions (default:zstd).zstdis smaller and faster to read/write thanlzfat equal precision — seedocs/optimizations.md.--n-snps-bw-bpoints N— target mean number of SNPs between consecutive breakpoints; controls block granularity (default: 10000, following Berisa & Pickrell 2016). The target breakpoint count isceil(n_snps / N - 1). Mutually exclusive with--n-bpoints.--n-bpoints N— directly specify the number of breakpoints, bypassing the--n-snps-bw-bpointsformula; useful when replicating a published analysis with a known block count--subset {fourier,fourier_ls,uniform,uniform_ls}— which of the four breakpoint sets to write to the BED file (default:fourier_ls; seedocs/pipeline-steps.mdstep 4)--all-breakpoint-subsets— compute all four breakpoint sets in the JSON output. By default,runcomputes only the requested--subsetand its dependencies to avoid unused local-search work.--workers N— parallel workers for the pipeline (default: 1); set to the number of available cores to speed up covariance calculation (step 2) and, unless overridden below, matrix-to-vector, local search, and metric scoring as well--matrix-workers N— override parallel workers for matrix-to-vector partition processing (default: inherit--workers)--local-search-workers N— override parallel workers for local search (default: inherit--workers). Higher values can multiply RAM use because each worker loads its own covariance window.--metric-workers N— override parallel workers for streaming metric row passes during breakpoint scoring (default: inherit--workers)--high-precision— use 50-digit Decimal arithmetic for local search instead of the default float path (slower; mainly useful for exact reference comparisons)
Each of the five stages (partition, covariance, matrix-to-vector, find-minima, extract-bpoints) can also be run individually, along with a covariance-summary inspection utility — see docs/pipeline-steps.md.
Interpolate genetic maps
Convert a recombination rate map (e.g. the deCODE map or HapMap-interpolated 1000G maps) to per-SNP genetic positions required by steps 1 and 2:
uv run ldetect interpolate-maps \
--snp-file snps.bed.gz \
--genetic-map recombination_map.gz \
--output chr2.interpolated_genetic_map.gz
Arguments:
--snp-file PATH— bgzipped BED file of SNP positions (columns:chrom start end rs_id); typically extracted from a filtered VCF withbcftools query -f '%CHROM\t%POS0\t%POS\t%ID\n'--genetic-map PATH— gzipped recombination map; interpolation is used to assign a cM value to each SNP position--output PATH— gzipped output map in the 3-column format expected by steps 1 and 2 (rs_id position cM)--mode {point,interval}(default:point) — interpolation algorithm:point— treats--genetic-mapas discrete(position, cM)points and linearly interpolates between the two points bracketing each SNP. Correct for point-sampled maps (e.g. HapMap-interpolated 1000G maps).interval— treats each map row as the start of a genomic interval with its own recombination rate (Begin, rate_cM_Mb, cumulative_cM_at_End), matching MacDonald et al.'s R interpolation scripts (interpolate.R/interpolate_pyhro.R). Required for interval-rate maps such as the deCODE map — feeding those intopointmode silently uses the next interval's rate for SNPs in the current interval, an off-by-one bug that produced a ~0.001–0.003 cM error per SNP in earlier testing (seenotes/findings/macdonald2022-reproduction.md).
Algorithm
The pipeline detects LD block boundaries by finding local minima in a smoothed diagonal-sum signal derived from the shrinkage LD covariance matrix:
- Partition — chromosome split into ~5000-SNP overlapping windows at low-recombination boundaries
- Covariance — Wen & Stephens shrinkage estimator applied to phased haplotypes; shrinks sample correlations toward the expected LD decay to reduce finite-sample noise
- Matrix → vector — each covariance matrix reduced to a
[position, diagonal_sum]signal; troughs correspond to LD block boundaries - Find minima — binary search for optimal Hanning-window filter width;
scipy.signal.argrelextremafinds local minima; local search refines each breakpoint using sum of squared inter-block correlations as the quality metric - Extract — chosen breakpoint set written as BED
The available breakpoint sets are fourier and uniform (raw minima from Fourier-filtered and uniformly-spaced candidates), plus fourier_ls and uniform_ls (after local search refinement). fourier_ls is the recommended output.
Known limitations
ldetect-lite reproduces the published Berisa & Pickrell (2016) 1000 Genomes LD blocks exactly for ASN (all 22 autosomes) and AFR (all chromosomes except chr22), and matches EUR block counts and coverage exactly but with shifted internal boundaries on chr8–chr12. These two residual divergences (EUR chr8-12, AFR chr22) are understood to stem from an unidentified upstream input/provenance difference from the original authors' pipeline, not a bug in this implementation — an extensive diagnostic effort ruled out VCF release-version provenance, SNP filtering, genetic map family, Ne assignment, duplicate/cross-partition handling, and reference-BED integrity as causes. See notes/findings/ldetect-original-reproduction.md for the full writeup, and notes/findings/macdonald2022-reproduction.md for the equivalent status reproducing MacDonald et al. (2022)'s GRCh38 blocks.
Pre-computed LD blocks
Pre-computed BED files for 1000 Genomes reference populations are available from in hg19 coordinates from the original LDetect data repository and in hg38 coordinates from a more recent effort by MacDonald et al. (2022).
BED files produced by our work will be released once the code base leaves alpha/finish major breaking updates.
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