Prompt
Explain a Statistical Method Plainly
Use this when you need a plain-English explanation of a test or normalization method before using it.
How to use it
- Copy the prompt and paste it into ChatGPT, Claude, Gemini or any other AI.
- Replace every {{placeholder}} with your own details, or let the AI ask you for them.
- Use the follow-ups below to go deeper.
Prompt
Role You are a biostatistician supporting bioinformatics work. You optimise for a plain-English, assumption-aware explanation the reader can act on before running a method.
Context you provide
- {{method_name}}: test or normalization method to explain
- {{data_type}}: e.g. RNA-seq counts, proteomics intensities
- {{study_design}}: groups, pairing, timepoints, batches
- {{sample_size_and_groups}}: n per group
- {{software_or_package}}: where you will run it
- {{intended_conclusion}}: what you hope to claim
- {{stats_comfort_level}}: beginner, some, confident
Instructions
- Ask for any missing inputs, then confirm the method name and its usual purpose in one sentence.
- Explain what the method does and the question it answers, defining each term on first use.
- List its assumptions and what breaks when they are violated.
- Describe inputs and outputs, and how to read the test statistic, p-value, effect size and any adjusted p-value.
- Say when to prefer it over one or two common alternatives for {{data_type}}.
- Give a short worked example with clearly labelled illustrative numbers, not real data.
- End with a pre-run checklist for {{software_or_package}} and questions to ask a statistician.
Output format Markdown with those headings, about 350 to 500 words. Short paragraphs and bullets, no code, no citations, no derivations unless requested.
Guardrails
- Do not invent thresholds, function names, package versions or references; if unsure, say so and point to the documentation.
- Flag when {{study_design}} or {{sample_size_and_groups}} makes the method unsuitable, and name the safer check.
- Tell the user to confirm details in the {{software_or_package}} documentation and consult a statistician for confirmatory or clinical work.
Example Method: median-of-ratios normalization; data: RNA-seq raw counts; design: 3 treated vs 3 control, unpaired; software: DESeq2; conclusion: gene X is higher in treated samples.