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Bio Long Read Sequencing Structural Variants

Agent skill
1 skill
READMEOverview ↓

Detects structural variants (deletions, insertions, inversions, duplications, translocations) from Oxford Nanopore and PacBio long-read alignments with Sniffles2, cuteSV, SVIM, and assembly-based callers, joint-genotypes cohorts via the Sniffles2 .snf workflow, and benchmarks with Truvari against GIAB. Covers why an SV call is a representation artifact (the tandem-repeat BED, aligner, and Truvari params set precision/recall as much as the caller), the cuteSV per-platform parameter trap, soft-clipped supplementary alignments as the SV substrate, and the somatic/mosaic boundary to Severus/nanomonsv. Use when calling germline or somatic SVs from ONT/HiFi reads, joint-genotyping a cohort, choosing or tuning an SV caller, or benchmarking SV calls.

Install with
Claude CodeCodexCursorGitHub CopilotGemini CLI

Supported by the Atlas install prompt. Skill-specific requirements vary.

Skill stats

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About this skill

Detects structural variants (deletions, insertions, inversions, duplications, translocations) from Oxford Nanopore and PacBio long-read alignments with Sniffles2, cuteSV, SVIM, and assembly-based callers, joint-genotypes cohorts via the Sniffles2 .snf workflow, and benchmarks with Truvari against GIAB. Covers why an SV call is a representation artifact (the tandem-repeat BED, aligner, and Truvari params set precision/recall as much as the caller), the cuteSV per-platform parameter trap, soft-clipped supplementary alignments as the SV substrate, and the somatic/mosaic boundary to Severus/nanomonsv. Use when calling germline or somatic SVs from ONT/HiFi reads, joint-genotyping a cohort, choosing or tuning an SV caller, or benchmarking SV calls.

Quick start

  1. Copy the install prompt. Use the green button above this README.
  2. Send it to your agent. Paste it into your coding agent’s chat and send.
  3. Review the setup. Your agent checks the skill’s instructions, requirements, and installation scope.

Installation guide →

Review, license & listing details
Review the source before using this skill

This is an imported listing. We haven’t certified its safety, license, or compatibility. Skills may include executable scripts.

Automated security scan: Partial

Only SKILL.md was scanned. Supporting files and scripts were not checked. No safety grade has been assigned.

0 potential findings · Scanned 11/4/2026 · Scanner 0.2.1

Content SHA-256: 302a73e124a3ad7c3deea9a2cd8e062a586231268656f79ecfeeb8dd1fb9c0bf

About scan coverage and limitations
Original listing metadata

Original name

bio-long-read-sequencing-structural-variants

Original description

Detects structural variants (deletions, insertions, inversions, duplications, translocations) from Oxford Nanopore and PacBio long-read alignments with Sniffles2, cuteSV, SVIM, and assembly-based callers, joint-genotypes cohorts via the Sniffles2 .snf workflow, and benchmarks with Truvari against GIAB. Covers why an SV call is a representation artifact (the tandem-repeat BED, aligner, and Truvari params set precision/recall as much as the caller), the cuteSV per-platform parameter trap, soft-clipped supplementary alignments as the SV substrate, and the somatic/mosaic boundary to Severus/nanomonsv. Use when calling germline or somatic SVs from ONT/HiFi reads, joint-genotyping a cohort, choosing or tuning an SV caller, or benchmarking SV calls.

About this listing

Category
General
Reported license
Not specified
Listing language (estimated)
English
Review status
Not individually reviewed
Agent compatibility
Atlas installation supports Claude Code, Codex, and Cursor. Skill-specific dependencies and features are checked during setup.
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Bio Long Read Sequencing Structural Variants | Agent Skills Atlas