PERSONAL RESEARCH LAB

Investigate your symptoms and genetic findings with your biology.

An open sourced personal research lab for your biology. Runs on your machine.

Install Genomi to access GenomiLab

Install and configure Genomi by following the instructions here: https://raw.githubusercontent.com/exon-research/genomi/master/INSTALL_FOR_AGENTS.md
See how it works

Uses your existing Genomi genome profile—no new VCF upload for every investigation.

Research support, not diagnosis or treatment. Findings may require professional or laboratory confirmation.

INVESTIGATION / SYNTHETIC EXAMPLE LOCAL GENOME
01 · PATIENT MOLECULAR PROFILE
Hypertrophic cardiomyopathy
Existing genomeReported MYH7 findingSymptoms reviewed
02 · EVIDENCE STREAMS
Published researchClinical evidenceMolecular evidenceSpecialized analysis
03 · INVESTIGATION
Candidate explanation
+ Supporting evidence− Counterevidence? Unanswered questions
04 · INVESTIGATION BRIEF
Updated · v0.4
SOURCE-LINKED
YOUR BIOLOGY · MANY HEALTH QUESTIONS

Research your health with your biology.

Keep your biological findings, symptoms, reports, and scientific sources together for each health question.

SYNTHETIC EXAMPLECould a reported MYH7 finding help explain hypertrophic cardiomyopathy, and what evidence or testing would clarify that link?
FROM QUESTION TO BRIEF

See how one question becomes a research brief.

GenomiLab connects your biology, health records, and scientific sources—then shows what fits, what conflicts, and what still needs confirmation.

GENOMILAB / INVESTIGATION PATHSYNTHETIC EXAMPLE · NO PATIENT DATA
  1. 01
    YOUR CONTEXT

    Use what is already in Genomi

    Your genetic findings, symptoms, health reports, and lab results form the starting point.

    LOCAL PROFILE
  2. 02
    ONE QUESTION

    Ask a specific health question

    Could a reported MYH7 finding help explain hypertrophic cardiomyopathy?

    SYNTHETIC EXAMPLE
  3. 03
    EVIDENCE CHECK

    Test the explanation against evidence

    Your agent compares published studies, clinical context, other genes, and competing explanations.

    SOURCES ATTACHED
  4. 04
    NEXT STEPS

    See what still needs confirmation

    Lab confirmation, family history, and unrecorded symptoms stay open instead of being guessed.

    CONFIRMATION NEEDED
WHAT YOU GET

Investigation Brief

v0.4UPDATED

Could a reported MYH7 finding help explain hypertrophic cardiomyopathy?

What supports the link
Gene–condition evidence and relevant published studies
What weakens the link
Some reported features do not match
What is still missing
Clinical lab confirmation and family history
What to ask next
Which tests or findings would change the interpretation?
12 SOURCE LINKSCONFIRMATION NEEDED

Your AI agent does the research. GenomiLab saves what it searched, found, questioned, and summarized for you.

  • Claude Code
  • Codex
  • OpenClaw
  • Hermes Agent
QUESTIONS YOU CAN ASK

Start with a question about your health.

Investigate a condition, symptom, genetic finding, missing test, or question for a specialist.

  1. 01

    Could this MYH7 finding help explain hypertrophic cardiomyopathy?

  2. 02

    What evidence supports or weakens that link?

  3. 03

    What other genes could be relevant to these symptoms?

  4. 04

    Which findings are established, uncertain, or not actionable?

  5. 05

    Which tests or medical records are still missing?

  6. 06

    What should I ask a specialist or laboratory?

WHY GENOMILAB

Keep your research in one place.

Replace disconnected reports and one-off AI answers with one saved research trail.

01
Static reportInvestigation that updates
02
Scattered recordsOne organized profile
03
One-off AI answerResearch your agent can continue
04
Single conclusionEvidence for, against, and missing
05
Repeated uploadsReuse your local genome
06
Hidden reasoningSources you can inspect
HOW IT WORKS

How GenomiLab researches your question.

Your installed AI agent works through five research roles—assembling the case, finding sources, challenging explanations, and saving a brief you can inspect.

CASE QUESTION · SYNTHETIC EXAMPLE

Could a reported MYH7 finding help explain hypertrophic cardiomyopathy?

LOCAL CONTEXT
ONE AGENT · FIVE RESEARCH ROLES

Context and citations carry forward through every role.

  1. 01
    CONTEXT MAPPERUSES YOUR GENOMI PROFILE

    Gather the facts that matter

    Find the genetic results, symptoms, reports, family history, and missing details relevant to the question.

  2. 02
    EVIDENCE RESEARCHERSOURCE-LINKED

    Find research for each lead

    Search published studies, clinical references, and disease databases, then save every relevant source.

  3. 03
    EVIDENCE ANALYSTFOR · AGAINST · UNCERTAIN

    Compare your case with the evidence

    Separate what supports an explanation, what conflicts with it, and what the research cannot answer yet.

  4. 04
    SKEPTICAL REVIEWERGAPS STAY VISIBLE

    Challenge the leading explanation

    Test alternatives and flag unconfirmed results, missing records, and evidence that does not fit.

  5. 05
    RESEARCH EDITORSAVED · VERSIONED

    Turn the work into a clear brief

    Write a plain-language summary with citations, open questions, and points to discuss with a qualified professional.

WHAT GENOMILAB SAVESSource-linked investigation brief
Sources
12
Conflicts
2
Open gaps
3
Version
0.4
HOW THE PARTS WORK TOGETHER

Your biology guides the question. Your AI agent does the research.

Genomi keeps your biological data local. GenomiLab organizes the evidence and summary. Your installed agent runs the investigation.

01

Genomi

Keeps your genome indexed on your machine so you can reuse it without uploading the raw file.

LOCAL GENOME
02

GenomiLab

Organizes each health question, its evidence, possible explanations, missing information, and updated summary.

ORGANIZED INVESTIGATION
03

Your AI agent

Runs the searches and analyses using tools such as Claude Code, Codex, OpenClaw, or Hermes Agent.

RESEARCH WORK
WHAT GENOMILAB SAVES

Everything saved for each question.

Your reviewed information, sources, possible explanations, missing details, and latest summary stay together.

01

Your health and biology profile

Relevant genetic findings, symptoms, reports, test results, and samples in one place.

REUSABLE PROFILE
02

A workspace for each question

A saved research thread for one condition, symptom, or result, including its history and open questions.

SAVED INVESTIGATION
03

Evidence for and against

Sources, possible explanations, conflicting findings, and missing information kept separate and visible.

UNCERTAINTY VISIBLE
04

An updated investigation brief

A plain summary that changes when you add information or your agent finds new evidence.

READY TO REVIEW
WHAT IT HELPS WITH

What you can learn from an investigation.

See relevant findings, evidence for and against an explanation, missing tests, and questions for a professional.

01

Put a genetic result in context

Compare it with your symptoms, test method, and published evidence.

02

Explore possible explanations

See which genes and biological pathways may be relevant without treating a possibility as a diagnosis.

03

See evidence for and against

Compare supporting sources, conflicting findings, and unanswered questions.

04

Prepare for a professional conversation

Turn the research into source-linked notes and questions for a specialist or laboratory—not treatment advice.

05

Find what still needs testing

Identify missing records, untested features, assay limits, and findings that need confirmation.

06

Track changes over time

See how the summary changes when new results or new research arrive.

HOW EVIDENCE IS HANDLED

See why an explanation may—or may not—fit.

GenomiLab separates supporting evidence, conflicting evidence, and missing information, with links to each source.

MOLECULAR OBSERVATION01

MYH7 finding reported in your biological data

Present in the existing Genomi profile. A confirmatory lab report was not provided.

OBSERVED · UNCONFIRMED
PUBLISHED RESEARCH02

Research links MYH7 to hypertrophic cardiomyopathy

This supports a possible connection, but does not show that this finding explains the condition.

SUPPORTING
CLINICAL CONTEXT03

Some expected features are not reported

This weakens the fit, but the current health record may be incomplete.

NOT ASSESSED
CANDIDATE EXPLANATION · SYNTHETIC

The MYH7 finding may be relevant, but it needs confirmation.

Published research supports a possible link. Missing lab confirmation and family testing prevent a stronger conclusion.

What supports it
Gene–condition link and published studies
What weakens it
Not all reported features match
What was not checked
Family inheritance and full test coverage
What needs confirmation
The finding and its clinical significance
CONFIRMATION NEEDED
YOUR INVESTIGATION BRIEF

Get a clear summary with links to evidence.

It records findings, uncertainty, missing tests, and questions for a qualified professional, then updates as evidence changes.

INVESTIGATION BRIEF

Could a reported MYH7 finding help explain hypertrophic cardiomyopathy?

v0.4UPDATED
SYNTHETIC EXAMPLE · RESEARCH SUPPORT ONLY · CONFIRMATION NEEDED
01 · RELEVANT MOLECULAR OBSERVATIONS

A reported MYH7 finding overlaps a gene linked to hypertrophic cardiomyopathy. Original lab evidence is unavailable.

02 · CANDIDATE MECHANISM

Published research supports a possible connection but does not prove the finding explains this person's condition.

SUPPORTING
  • MYH7–condition link
  • Relevant published research
COUNTEREVIDENCE
  • Some features do not match
  • Inheritance unknown
03 · MISSING TESTS OR INFORMATION

Confirmatory testing, family history, and a structured symptom review.

04 · QUESTIONS FOR A QUALIFIED PROFESSIONAL

Should the MYH7 finding be confirmed in a clinical lab, and which symptoms or family results would change its interpretation?

12 EVIDENCE LINKSVERSION HISTORY · 4
PRIVACY AND CONTROL

Keep your raw genome on your machine.

GenomiLab uses the local genome index already built by Genomi. It does not upload your genome again for each question.

If an external model or evidence service is needed, you see and approve the exact information before it is sent.

YOUR MACHINE
Existing Genomi profileraw genome · local index
STAYS LOCAL
APPROVAL GATEOnly the shown, approved context crosses
WHEN NEEDED
Evidence serviceExternal model
AVAILABLE WITH GENOMI

Install Genomi to start an investigation.

Research a condition, symptom, or genetic finding while keeping sources, uncertainty, and missing information visible.

Install Genomi to access GenomiLab
Install and configure Genomi by following the instructions here: https://raw.githubusercontent.com/exon-research/genomi/master/INSTALL_FOR_AGENTS.md
See Genomi first