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SKILL verified MIT Self-run

Bioresearch Ld Reference Management

skill-alim430-bioresearch-agent-ld-reference-management · by Alim430

Manage ancestry-specific LD reference panels and perform LD clumping for cross-ancestry MR. Use when the user needs to simulate ancestry-aware LD block structures (AFR/EUR/EAS/SAS/AMR), run greedy distance-based clumping (PLINK --clump style), or compute LD scores for stratified LDSC. Mock mode validates the clumping pipeline; live mode wraps PLINK 2.0 + 1000 Genomes reference panels.

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Install

$ agentstack add skill-alim430-bioresearch-agent-ld-reference-management

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Security review

✓ Passed

No issues found. Passed automated security review. · v0.1.0 How review works →

  • Prompt-injection patterns
  • Secret / credential exfiltration
  • Dangerous shell & filesystem operations
  • Untrusted network calls
  • Known-malicious package signatures

What it can access

  • Network access No
  • Filesystem access No
  • Shell / process execution No
  • Environment & secrets No
  • Dynamic code execution No

From automated source analysis of v0.1.0. “Used” means the capability is present in the source — more access means more to trust, not that it’s unsafe.

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Reliability & compatibility

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Declared compatibility

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About

BioResearch Agent — LD Reference Panel Management Skill

Capability

Manages ancestry-specific LD reference panels and performs LD-based instrument clumping:

  1. Ancestry-aware LD simulation — generates realistic LD block structures for 5 super-populations

(AFR / EUR / EAS / SAS / AMR) with biologically grounded parameters: AFR has shortest LD blocks (older population, more recombination), non-AFR populations have longer blocks (serial founder effects). Block lengths and LD decay rates follow 1000 Genomes empirical patterns.

  1. Greedy LD clumping — PLINK --clump-style algorithm: sort SNPs by p-value, greedily select

lead SNPs, remove proxies within a distance + r² threshold. Returns independent instrument set.

  1. LD score computation — per-SNP LD scores (sum of r² with neighbors) for stratified LDSC

heritability partitioning across ancestries.

  1. Cross-ancestry LD comparison — pairwise LD decay curves and block-length distributions,

quantifying how LD structure differs across populations (the root cause of ancestry-portability failure in MR).

Returns a clumped instrument set + LD score table + ancestry comparison report, not a causal claim.

Run

bioresearch run ld-reference-management --ancestry EUR --n-snps 500 --seed 42 --output-dir outputs/ld-reference

Outputs (in --output-dir)

  • ld_clumped_instruments.csv — independent lead SNPs after clumping (SNP, CHR, POS, P, cluster_id)
  • ld_scores.csv — per-SNP LD scores per ancestry (SNP, ancestry, ld_score)
  • ld_decay_comparison.csv — pairwise LD decay curves (distance, meanr2, ancestrypair)
  • ld_block_summary.csv — per-ancestry block-length statistics (mean, median, max, n_blocks)
  • ld_ancestry_heatmap.png — LD decay heatmap across ancestries
  • ld_evidence_package.json — reproducible Evidence Package (provenance + parameters + grade)

Note

This skill dispatches to the framework's ld-reference-management workflow / demo_ld_reference.py. It adds no analysis of its own; all computations run in the workflow modules. By default uses simulated LD panels with ancestry-specific parameters to validate the clumping pipeline — real-data deployment would use PLINK 2.0 with 1000 Genomes Phase 3 reference panels per ancestry. Evidence grade is C (methodology validation). Part of Phase 3a (cross-ancestry MR, CPU-only).

Source & license

This open-source skill is cataloged on AgentStack and links to its original source — we do not rehost the code.

Install and usage instructions live in the source repository linked above.

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Versions

  • v0.1.0 Imported from the upstream source.