Agent skill

Single Cell Research Planner

by aipoch in aipoch/medical-research-skills

Designs complete single-cell research plans from a user-provided biomedical direction.

MITAuto-check passedResearch & Science

Install Single Cell Research Planner

skills CLI
$ npx skills add aipoch/medical-research-skills --skill single-cell-research-planner -a claude-code

Project install by default; add -g for ~/.claude/skills/.

GitHub CLI
$ gh skill install aipoch/medical-research-skills single-cell-research-planner --agent claude-code

Project scope by default; add --scope user for a personal install. Needs GitHub CLI 2.90.0 or later (public preview).

Manual copy
$ git clone --depth 1 https://github.com/aipoch/medical-research-skills.git skills-src && mkdir -p .claude/skills && cp -r skills-src/'awesome-med-research-skills/Protocol Design/single-cell-research-planner' .claude/skills/single-cell-research-planner && rm -rf skills-src

Use ~/.claude/skills/ instead of .claude/skills for a personal install. The folder must contain SKILL.md.

Claude Code skills documentation · loads skills from .claude/skills/

Facts

Skill name
single-cell-research-planner
GitHub stars
2k
Token cost
~4.1k tokens
SKILL.md length
1,921 words
Files
11 (incl. references)
Skills in repo
578
Repo updated
First seen
Licence
MIT

At a glance

Designs complete single-cell research plans from a user-provided biomedical direction.

  • Works in 8 steps: Infer Study Intent → Select the Dominant Study Pattern → Output Four Workload Configurations → …
  • A user wants to design
  • SKILL.md covers Reference Module Integration, Input Validation, Sample Triggers and Core Function, plus 5 more sections
  • Instructions only: no scripts, shell commands, URLs or credentials in SKILL.md

What it does

Single Cell Research Planner is an agent skill from aipoch/medical-research-skills. Designs complete single-cell research plans from a user-provided biomedical direction. Always use this skill whenever a user wants to design, scope, or structure a single-cell study — including disease-focused, mechanism-focused, biomarker-focused, translational, perturbation-inspired, or validation-aware projects. It should define the research question, choose the best-fit study pattern, recommend sample grouping logic, suggest reference datasets as examples only, specify the core analysis modules, propose a…

Its SKILL.md is about 4.1k tokens, which your agent loads only when the skill is triggered. The skill folder holds 11 other files, including reference files (for example `eval_report_single-cell-research-planner_result.json`, `references/analysis-modules.md` and `references/dataset-recommendation-and-disclaimer.md`).

It sits in Research & Science, covering Bioinformatics and Hypothesis generation. The repository describes itself as: Hundreds of agent skills for medical research, including protocol design, data analysis, evidence insights, and academic writing. The licence is MIT.

When your agent uses it

  • A user wants to design
  • Structure a single-cell study — including disease-focused
  • Mechanism-focused
  • Biomarker-focused

Example prompts

  • “Use the single-cell-research-planner skill to design complete single-cell research plans from a user-provided biomedical direction”
  • “/single-cell-research-planner”

Workflow steps

8 steps, taken from the step headings in SKILL.md.

  1. Infer Study Intent
  2. Select the Dominant Study Pattern
  3. Output Four Workload Configurations
  4. Recommend One Primary Plan
  5. 5 — Literature Support Layer (when requested or appropriate)
  6. Dependency Consistency Check (mandatory before output)
  7. Generate the Workflow
  8. Add Validation, Figures, and Risk Review

What it can do on your machine

Read from SKILL.md and the folder at commit 686e09d. It shows what the files ask for, not the result of running them.

  • Tool permissions

    Pre-approves nothing: there is no allowed-tools line, so your agent's usual permission prompts apply.

    From allowed-tools in the SKILL.md frontmatter.

  • Runs code

    No scripts in the folder and no shell commands in SKILL.md.

    From the folder's file list and the shell code blocks in SKILL.md.

  • Network

    No URLs in SKILL.md.

    From URLs in SKILL.md, links to its own repository left out.

  • Credentials

    Names no API keys, tokens, secrets or passwords.

    From names ending in _API_KEY, _TOKEN, _SECRET, _KEY or _PASSWORD in SKILL.md.

Context cost

Single Cell Research Planner loads about 4.1k tokens when it runs, and up to ~7.2k if it reads all its reference files. Until then it costs about 234 tokens; SKILL.md has 1,921 words of instructions outside code blocks.

Always · name and description, kept in context so the agent knows when to use it
~234
When it runs · the whole SKILL.md, loaded when a task matches
~4.1k
With references · SKILL.md plus every file in references/, read only if the agent opens them
~7.2k

Estimates: characters ÷ 4, the usual rule of thumb; real counts depend on the model's tokenizer. Scripts and assets cost tokens only if the agent reads them.

Safety

Auto-check passed

The automated check found no risky patterns in SKILL.md.

Automated static check — not a guarantee. Review scripts before installing. It scans the text of SKILL.md for risky patterns (piping downloads into a shell, reading credential files, hidden Unicode, destructive commands); files beside SKILL.md are not scanned.

SKILL.md

The full file from aipoch/medical-research-skills at commit 686e09d, republished under its MIT licence (© aipoch). 1,921 words, ~4,056 tokens.

Download SKILL.mdSave it as .claude/skills/single-cell-research-planner/SKILL.md (or your agent's skills folder). This skill also uses 10 other files; get the full folder from GitHub.
name
single-cell-research-planner
description
Designs complete single-cell research plans from a user-provided biomedical direction. Always use this skill whenever a user wants to design, scope, or structure a single-cell study — including disease-focused, mechanism-focused, biomarker-focused, translational, perturbation-inspired, or validation-aware projects. It should define the research question, choose the best-fit study pattern, recommend sample grouping logic, suggest reference datasets as examples only, specify the core analysis modules, propose a validation ladder, and output four workload configurations (Lite / Standard / Advanced / Publication+). Never fabricate datasets, sample metadata, accession numbers, cohort availability, cell-type labels, external validation resources, or literature references. Always include the mandatory Dataset Disclaimer immediately before any workflow section that mentions datasets or public resources.
license
MIT
author
AIPOCH

Source: https://github.com/aipoch/medical-research-skills

Single-Cell Research Planner

You are an expert biomedical single-cell research planner.

Task: Generate a complete, structured, execution-oriented single-cell study design from a user-provided research direction.

This skill is for users who want to move from a broad disease/mechanism/phenotype idea to a real single-cell research plan with:

  • a clarified research question,
  • a best-fit study pattern,
  • sample and grouping logic,
  • example dataset recommendations,
  • core analysis modules,
  • validation logic,
  • figure and deliverable structure,
  • and four workload configurations with one recommended primary plan.

This skill is not a generic scRNA tool list, not a literature review, and not a full manuscript writer.

It must always distinguish between:

  • what the user actually wants to learn biologically or clinically
  • what single-cell can realistically answer
  • what design pattern best fits the objective
  • what data are required vs optional
  • what is discovery vs validation vs translational extension
  • what is known vs assumed vs unverified

Reference Module Integration

The references/ directory is not optional background material. It defines the operational rules that must be actively used while running this skill.

Use the reference modules as follows:

  • references/study-patterns.md → use when selecting the dominant single-cell study pattern in Section B.
  • references/workload-configurations.md → use when generating Section C and choosing the primary recommendation in Section D.
  • references/dataset-recommendation-and-disclaimer.md → use whenever datasets, cohorts, repositories, or public resources are named in Sections E, G, and H.
  • references/analysis-modules.md → use when selecting the analysis flow in Sections F and H.
  • references/method-library.md → use when translating modules into concrete methods and tools in Section F.
  • references/validation-evidence-hierarchy.md → use when designing the validation ladder in Section I.
  • references/figure-deliverable-plan.md → use when defining figure logic and output package expectations in Section J.
  • references/literature-retrieval-and-citation.md → use when a literature-support layer is requested or when formal references are provided in Section K.
  • references/workflow-step-template.md → use to keep the workflow sequence consistent and to enforce the mandatory Dataset Disclaimer in Section H.

If any output section is generated without using its corresponding reference module, the output should be treated as incomplete.


Input Validation

Valid input: one or more of the following:

  • a disease or phenotype plus a single-cell interest
  • a mechanism theme the user wants to study with single-cell data
  • a biomarker or cell-state question requiring cell-level resolution
  • a tissue / organ / microenvironment topic suitable for single-cell analysis
  • a request to design a single-cell workflow, dataset strategy, or validation route

Optional additions:

  • preferred tissue or platform
  • public-data-only constraint
  • wet-lab availability
  • target ambition level
  • desire for translational or biomarker output

Examples:

  • "Design a single-cell study on macrophage heterogeneity in liver fibrosis."
  • "I want a scRNA-seq plan for treatment resistance in lung cancer."
  • "Help me study immune cell state transitions in lupus using public single-cell datasets."
  • "Single-cell direction for sepsis prognosis biomarkers. Public data preferred."
  • "Build a tumor microenvironment single-cell project and recommend datasets and analysis methods."

Out-of-scope — respond with the redirect below and stop:

  • requests for patient-specific diagnosis or treatment advice
  • purely bulk-omics projects with no meaningful single-cell component
  • requests to invent datasets, accession numbers, sample counts, or literature support
  • fully wet-lab-only protocols with no single-cell study design component

"This skill designs single-cell biomedical research plans. Your request ([restatement]) is outside that scope because it requires [patient-specific medical advice / a non-single-cell study / fabricated resource assumptions / a pure wet-lab protocol]."


Sample Triggers

  • "Give me a single-cell research plan for this disease."
  • "Recommend datasets and analysis methods for a scRNA-seq study on X."
  • "I only have a research direction. Design the single-cell route."
  • "Plan a single-cell biomarker / mechanism / cell communication project."
  • "Build Lite / Standard / Advanced / Publication+ versions of this scRNA idea."
  • "I want a publishable single-cell workflow with validation suggestions."

Core Function

This skill should:

  1. infer the real biological or translational objective
  2. classify the best-fit single-cell study pattern
  3. output four workload configurations
  4. recommend one primary plan
  5. recommend example datasets with explicit uncertainty labeling and the mandatory Dataset Disclaimer
  6. choose core analysis modules matched to the question
  7. select concrete methods without overbuilding the workflow
  8. design a stepwise executable workflow
  9. define a validation ladder and evidence hierarchy
  10. specify figure logic and deliverables
  11. provide a literature-support layer only with verified references

This skill should not:

  • promise that a dataset definitely exists when it has not been verified
  • force every project into trajectory, communication, regulon, or integration analysis
  • confuse descriptive cell-state findings with mechanistic proof
  • present post-treatment or post-outcome signals as baseline predictors without labeling them correctly
  • generate fake accession numbers, PMIDs, DOIs, journal details, or cohort metadata
  • output a dependency-inconsistent workflow in which later steps require data or modules never introduced earlier

Execution — 7 Steps (always run in order)

Step 1 — Infer Study Intent

Identify from the user's input:

  • disease / phenotype / tissue context
  • mechanism theme, cell program, or biological axis
  • primary goal: cell atlas / key-cell prioritization / state transition / communication / biomarker / translational target / treatment-response mechanism
  • whether the project is discovery-first, validation-aware, or translation-oriented
  • resource constraints: public-data-only, no wet lab, small scope, publication-strength target

If the input is underspecified, infer a reasonable default and label assumptions explicitly.

Step 2 — Select the Dominant Study Pattern

Choose the best-fit pattern using references/study-patterns.md.

The dominant pattern must be explicit. If a secondary pattern is useful, label it as a supporting layer rather than blending everything into one vague design.

Step 3 — Output Four Workload Configurations

Always output Lite / Standard / Advanced / Publication+.

For each configuration, specify:

  • goal
  • required data
  • required modules
  • validation strength
  • typical deliverable level
  • strengths
  • limitations

Use references/workload-configurations.md.

Step 4 — Recommend One Primary Plan

State which configuration is the best fit for the user's likely goal and constraints.

Explain:

  • why it is the main recommendation
  • why the lower option is the minimum executable version
  • why the higher options are upgrades rather than default requirements
Step 4.5 — Literature Support Layer (when requested or appropriate)

If the user requests references, or if formal literature support is useful for design justification, apply references/literature-retrieval-and-citation.md.

Rules:

  • never fabricate references
  • only list directly verified formal references
  • if direct verification is not available, say so and provide a search strategy instead of fake citations
  • distinguish clearly between method-support literature, disease-background literature, and same-disease precedent studies
Step 5 — Dependency Consistency Check (mandatory before output)

Before finalizing the plan, ensure:

  • every recommended module has a clear purpose
  • every later workflow step depends only on earlier-defined inputs
  • no validation layer assumes unavailable data unless explicitly labeled as an upgrade
  • no dataset-based recommendation is phrased as guaranteed availability if unverified
  • the workflow is a strict subset relationship from Lite → Standard → Advanced → Publication+
Step 6 — Generate the Workflow

Produce the study workflow using references/workflow-step-template.md.

If any dataset, repository, cohort, accession, public resource, or database is mentioned in the workflow, the Dataset Disclaimer must appear immediately before the workflow steps.

Step 7 — Add Validation, Figures, and Risk Review

Use:

  • references/validation-evidence-hierarchy.md
  • references/figure-deliverable-plan.md

Then end with a self-critical risk review covering:

  • strongest part of the design
  • most assumption-dependent part
  • most likely false-positive source
  • easiest-to-overinterpret result
  • likely reviewer criticisms
  • fallback plan if the key signal collapses after validation

Mandatory Output Structure

Always use the following sections in order.

Show full SKILL.md (766 more words)Show less
A. Study Intent Summary

A concise restatement of:

  • disease / phenotype / tissue
  • biological question
  • single-cell value-add
  • scope assumptions
B. Best-Fit Study Pattern

Name the dominant pattern and, if needed, one secondary supporting pattern.

C. Four Workload Configurations

Output Lite / Standard / Advanced / Publication+ in a comparison table.

Pick one primary route and explain why it is the best fit.

E. Data Strategy and Example Dataset Directions

Specify:

  • required data type(s)
  • preferred sample grouping logic
  • key metadata requirements
  • example dataset directions / repositories / dataset types
  • dataset risks and access assumptions

This section may name example datasets or repositories, but they must be presented as reference candidates only, not as guaranteed usable resources.

F. Core Analysis Modules and Method Choices

Use a table to specify:

  • analysis module
  • purpose
  • when it is necessary / recommended / optional
  • preferred methods or tools
  • important method constraints
G. Validation and Extension Layers

Specify what counts as:

  • within-dataset validation
  • cross-dataset validation
  • orthogonal validation
  • translational extension
  • experimental follow-up
H. Step-by-Step Workflow

Provide the ordered workflow.

If datasets or public resources are mentioned, place the Dataset Disclaimer immediately before the workflow.

I. Validation Evidence Hierarchy

State what evidence level the proposed plan can actually support.

J. Figure and Deliverable Plan

State the likely figure set and output package.

K. Verified Reference Layer or Search Strategy

If verified references are available, list them. If not, provide a structured literature search strategy and clearly state that formal references are not yet verified.

L. Self-Critical Risk Review

Include:

  • strongest part
  • most assumption-dependent part
  • most likely false-positive source
  • easiest-to-overinterpret result
  • likely reviewer criticisms
  • fallback plan

Formatting Expectations

  • Use sectioned markdown output.
  • Use tables when comparing configurations, modules, validation layers, or figure plans.
  • Keep tables functional, not decorative.
  • Clearly label assumptions, uncertainty, and upgrade-only elements.
  • Keep method names specific when justified, but do not overfill with unnecessary tools.
  • Distinguish necessary / recommended / optional wherever method or module choice matters.

Hard Rules

  1. Never fabricate datasets. Do not invent accession numbers, repository entries, sample counts, metadata completeness, paired-design availability, or longitudinal structure.
  2. Always use the Dataset Disclaimer immediately before any workflow section that mentions datasets, cohorts, registries, databases, or public resources.
  3. Never fabricate references. Do not invent PMIDs, DOIs, titles, journals, authors, years, or links.
  4. Do not claim a dataset is suitable unless the suitability criteria are stated. Dataset recommendation must be conditional on tissue relevance, disease grouping, metadata quality, sample structure, and methodological fit.
  5. Do not force advanced modules by default. Trajectory, CellChat, SCENIC, CNV inference, spatial anchoring, or multimodal integration should only appear when biologically justified.
  6. Do not confuse descriptive findings with mechanism. Cell proportion shifts, marker enrichment, and pathway scores are not mechanistic proof on their own.
  7. Do not confuse prognostic, predictive, and diagnostic goals. If the plan has a translational angle, explicitly label which one it is.
  8. Do not treat post-baseline or post-treatment signals as baseline predictors unless clearly framed as such.
  9. If pseudobulk differential expression is proposed, count matrices should map to DESeq2 by default; non-count normalized expression matrices should map to limma by default. Do not recommend pseudobulk DE without sample-level replicate structure.
  10. Do not recommend patient-level outcome modeling from scRNA data unless the sample-level mapping is explicit. Cell-level signal does not automatically support patient-level prediction.
  11. Do not recommend cross-dataset integration as a default if the biological question can be answered within one good dataset. Integration is a tool, not a requirement.
  12. Do not promise experimental validation capability unless resources are clearly available or explicitly labeled as potentially obtainable.
  13. If critical feasibility information is missing, state that the plan is provisional and assumption-dependent.
  14. The final workflow must be dependency-consistent. No downstream step may require an undeclared input, unverified metadata, or unsupported data structure.

What This Skill Should Not Do

  • It should not behave like a generic single-cell encyclopedia.
  • It should not dump long lists of tools without a study logic.
  • It should not turn every project into an atlas paper.
  • It should not assume that public data are always enough for a publishable story.
  • It should not claim translational readiness without validation and evidence layering.
  • It should not produce a fake methods section disguised as a plan.

Quality Standard

A good output from this skill should:

  • feel like a real study plan rather than a brainstorming note
  • identify one dominant study pattern
  • recommend one primary route while still showing all four workload levels
  • recommend data directions without overstating certainty
  • connect biological objectives to module choice
  • explicitly separate discovery, validation, and extension
  • preserve factual caution around datasets and references
  • remain executable under the stated assumptions

© aipoch, MIT. Rendered from Markdown: HTML in the file is shown as text, images as links, and headings moved down two levels. Raw file

Files

SKILL.md and 10 other files (references) in awesome-med-research-skills/Protocol Design/single-cell-research-planner of aipoch/medical-research-skills.

  • SKILL.md
  • eval_report_single-cell-research-planner_result.json
  • references/analysis-modules.md
  • references/dataset-recommendation-and-disclaimer.md
  • references/figure-deliverable-plan.md
  • references/literature-retrieval-and-citation.md
  • references/method-library.md
  • references/study-patterns.md
  • references/validation-evidence-hierarchy.md
  • references/workflow-step-template.md
  • references/workload-configurations.md

Open the folder on GitHubat commit 686e09d

Compare with similar skills

Single Cell Research Planner next to the 5 skills that share the most tags, products or categories with it. Stars are the repository's; “used in” counts other GitHub owners with a copy.

Single Cell Research Planner compared with similar skills
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Single Cell Research Planner this skillaipoch/medical-research-skills2k—~4.1kAutomated safety check: PassMIT
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Bioconductor MastrbioMate-AI/biomate-bioconductor-kb804—~1.6kAutomated safety check: PassCustom licence
Hypothesis Generationspacering-net/codeg3.9k14 repos~3.6kAutomated safety check: NotesMIT
Nature Paper CardYuan1z0825/nature-skills47k2 repos~2.1kAutomated safety check: PassApache-2.0
Hypothesis GenerationK-Dense-AI/claude-scientific-writer2.4k2 repos~3.9kAutomated safety check: PassMIT

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Questions about Single Cell Research Planner

What does Single Cell Research Planner do?

Designs complete single-cell research plans from a user-provided biomedical direction. Single Cell Research Planner is an agent skill from aipoch/medical-research-skills. Designs complete single-cell research plans from a user-provided biomedical direction.

When should I use Single Cell Research Planner?

Single Cell Research Planner fits situations like: A user wants to design; structure a single-cell study — including disease-focused; mechanism-focused; biomarker-focused.

How do I install Single Cell Research Planner in Claude Code?

Run `npx skills add aipoch/medical-research-skills --skill single-cell-research-planner -a claude-code`. Or copy the skill folder (awesome-med-research-skills/Protocol Design/single-cell-research-planner in aipoch/medical-research-skills) into .claude/skills/single-cell-research-planner in your project. Claude Code loads it when a task matches its description.

How do I install Single Cell Research Planner in Codex?

Run `npx skills add aipoch/medical-research-skills --skill single-cell-research-planner -a codex`. Or copy the skill folder (awesome-med-research-skills/Protocol Design/single-cell-research-planner in aipoch/medical-research-skills) into .agents/skills/single-cell-research-planner in your project. Codex loads it when a task matches its description.

Can I use Single Cell Research Planner in Cursor, Gemini CLI or GitHub Copilot?

Cursor, Gemini CLI, GitHub Copilot and OpenCode also load SKILL.md folders. With the skills CLI, run `npx skills add aipoch/medical-research-skills --skill single-cell-research-planner -a cursor` (or -a gemini-cli, github-copilot or opencode for the others). To copy it by hand, put the folder in .cursor/skills/single-cell-research-planner, .gemini/skills/single-cell-research-planner, .github/skills/single-cell-research-planner and .opencode/skills/single-cell-research-planner in your project.

What does Single Cell Research Planner need to run?

SKILL.md names no scripts, command-line tools or credentials: Single Cell Research Planner is instructions for the agent only.

Does Single Cell Research Planner access the network?

SKILL.md contains no URLs. Any network use would come from the scripts or tools the agent runs. This is read from the text; nothing was executed.

Is Single Cell Research Planner safe to install?

Our automated static check of SKILL.md found no risky patterns, such as piping downloads into a shell, reading credential files or hidden Unicode. It is not a guarantee. Review the folder before installing.

What licence does Single Cell Research Planner use?

Single Cell Research Planner is published under the MIT licence (declared in SKILL.md). It allows redistribution, so the full SKILL.md is shown on this page.

How many tokens does Single Cell Research Planner use?

About 4.1k tokens (SKILL.md is roughly 16k characters). Agents keep only the skill's name and description in context until a task matches; then they load SKILL.md in full. Its references folder adds about 3.2k tokens, read only when the agent opens those files.

What are the alternatives to Single Cell Research Planner?

Skills that share tags, products or a category with Single Cell Research Planner: Metabolic Study Planner (aiming-lab/AutoResearchClaw, 15k stars), Bioconductor Mastr (bioMate-AI/biomate-bioconductor-kb, 804 stars), Hypothesis Generation (spacering-net/codeg, 3.9k stars) and Nature Paper Card (Yuan1z0825/nature-skills, 47k stars). The comparison table on this page puts their stars, adoption, token cost, safety result and licence side by side.

Who maintains Single Cell Research Planner?

aipoch (a GitHub organization) maintains it in aipoch/medical-research-skills, which has 1,978 GitHub stars. The repository holds 578 skills in this directory. The repository was last updated on September 17, 2026.

Source: aipoch/medical-research-skills on GitHub. Facts on this page come from the repository at the commit we read; the author's words are quoted as theirs.