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Copy Number Agent Skill

Workflow for copy-number estimation, segmentation, annotation, and visualization in sequencing-based assays.

1k tokens
context cost
SKILL.md, read when the skill is used
3
files
plus reference files
0
copies elsewhere
how many repositories repackaged it
132
stars on the repo
on the repository, not the skill itself

Install

one command, takes just this skill from the repository
npx skills add https://github.com/BioTender-max/awesome-bio-agent-skills --skill copy-number

What comes with it

2 438 bytes besides the instruction
README.md
references/technical_reference.md

The instruction itself

22 sections, as written by the author

Copy Number

Version Compatibility

Reference examples assume recent stable releases of the preferred tools, especially CNVkit-style and the other tools listed below.

Before using code or command patterns, verify installed versions match the environment:

  • Python: python -c "import <module>; print(<module>.__version__)"
  • CLI: <tool> --version
  • If signatures differ, inspect the installed help or API and adapt the pattern instead of retrying unchanged.

Overview

Workflow for copy-number estimation, segmentation, annotation, and visualization in sequencing-based assays.

When To Use This Skill

  • use when the task is CNV calling or copy-number visualization
  • use when coverage-based segment inference is needed for tumor or cohort samples
  • use when the user needs gene-level CNV summaries or segment plots

Quick Route

  • If the input is raw or minimally processed data, start with validation and QC before any modeling.
  • If the input is already processed, skip directly to the first workflow step that matches the user goal.
  • If the user asks for a biological conclusion, always produce at least one QC or confidence artifact alongside the final result.

Progressive Disclosure

  • Read references/technical_reference.md when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.
  • Keep SKILL.md as the main execution path and load the reference file only when the task or failure mode needs the extra detail.

Default Rules

  • Prefer Python-first workflows unless the task explicitly requires something else.
  • Keep intermediate and final outputs separated.
  • Record software versions, reference builds, and key parameters when they affect interpretation.
  • Favor reproducible tables and figures over one-off interactive-only outputs.

Expected Inputs

  • coverage or ratio data
  • target bins or intervals
  • sample metadata

Expected Outputs

  • CNV segments
  • gene-level CNV tables
  • CNV plots

Preferred Tools

  • CNVkit-style workflows
  • GATK CNV-style workflows
  • pandas
  • matplotlib

Starter Pattern

Preferred starting point: CNVkit-style
Inputs: coverage or ratio data, target bins or intervals, sample metadata
Outputs: CNV segments, gene-level CNV tables, CNV plots

Workflow

1. Confirm assay context

Clarify tumor-normal versus tumor-only design and target capture versus genome-wide coverage.

2. Generate or import coverage summaries

Build bin- or target-level signals suitable for segmentation.

3. Call segments

Infer copy-number segments and classify gains, losses, or focal events.

4. Annotate to genes and loci

Map segments to biologically relevant genes and recurrent regions.

5. Report with visualization

Produce chromosome-level plots and gene-centric summaries.

Output Artifacts

  • Recommended output layout:
  • results/ for final tables and serialized objects
  • figures/ for plots and static visual exports
  • qc/ for checks that justify downstream interpretation
  • Minimum expected outputs for this skill:
  • CNV segments
  • gene-level CNV tables
  • CNV plots

Quality Review

  • Confirm identifiers and metadata join correctly before modeling or summarizing.
  • Generate at least one QC artifact before final biological interpretation.
  • Keep raw or minimally processed inputs separate from transformed outputs.
  • Record reference build, caller assumptions, and filtering rules in the final outputs.
  • Separate raw calls from filtered or interpreted results.

Anti-Patterns

  • treating noisy ratio shifts as confident focal events without segmentation support
  • ignoring tumor purity or ploidy context when it matters
  • reporting copy-number calls without genome build and binning details
  • Variant Calling
  • Long-Read Genomics
  • Genome Assembly
  • Comparative Genomics

Optional Supplements

  • None required for the first pass.

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How to use it

Copy the folder

Take biotender-max/copy-number from the repository into ~/.claude/skills for personal use, or into .claude/skills inside a project.

Check the name does not clash

The agent identifies a skill by the name field in its header. Two skills with the same name cannot sit side by side — one of them will be ignored.