Tutorial
Use Genome Intelligence in your workflow
Learn how to move from a live research card into a deeper, file-grounded conversation with your own .genome.
What you will learn:
You will know how to copy a Genome Intelligence prompt, adapt it to your data, and follow the evidence in your own file.
Genome Intelligence and Tutorials have different jobs. Genome Intelligence is the evolving research layer: new papers, variants, genes, sources, and prompts. Tutorials are the workflow layer: how to take that research and explore it against your own .genome.
A good Genome Intelligence workflow does not stop at reading a card. You copy the prompt, run it against your .genome, ask what was found in your file, ask what came from the paper or source, and then decide what follow-up question would make the exploration more useful.
Research card workflow
- Open Genome Intelligence.
- Search for a topic, gene, variant, or category.
- Choose a card with a concrete research question and prompt.
- Read the source and the prompt before copying it.
- Paste the prompt into a session that has access to your
.genome. - Ask the model to identify which files and annotations it will inspect.
- Run the prompt and ask for file evidence, annotation context, and source context.
- Ask a follow-up question based on what was actually present in your file.
Apply a Genome Intelligence card
I copied this Genome Intelligence prompt: [paste prompt]. Apply it to my .genome bundle. First identify the relevant files, genes, variants, annotations, and sources. Then answer the prompt using my data where available, and separate my file evidence from the research context behind the card.
Create follow-up questions
Based on the answer, give me five follow-up questions. For each question, explain which part of my .genome bundle you would inspect next and what kind of evidence would make the answer stronger.
What to preserve from the card
- The specific gene, variant, pathway, or research mechanism.
- The source or paper behind the card.
- The exact question the prompt is asking.
- The distinction between research evidence and personal file evidence.
- The follow-up path into your own
.genome.
This workflow is the bridge between latest research and personal exploration. Genome Intelligence tells you what is newly useful. Your .genome tells you what can be inspected in your own data. The AI helps you move between the two.