Symptom-Driven Whole-Genome Exploration
Your Symptoms Have a Story. Your Genome May Help Explore Why.
EvaGenomics brings your symptoms and whole-genome information together through Deep Analysis to provide educational insights, clearer questions, and a more informed direction for your next healthcare conversation.
EvaGenomics provides educational genomic information. It does not diagnose, treat, or replace care from a qualified healthcare professional.
Symptoms organized around your story
Your reported symptoms are grouped to help reveal patterns across body systems.
Questions for your doctor included
Designed to support clearer, more confident healthcare conversations.
Symptom-Driven Approach
Your reported symptoms guide the genomic review.
Whole-Genome Sequencing
A broader view than a limited gene or condition-specific panel.
Designed for Reanalysis
Genomic information may be reviewed again as science advances.
Your Data. Your Choice.
Clear consent and transparent data-use options.
Why Genetic Information Matters
Your symptoms may be connected in ways that separate tests cannot always show.
Symptoms affecting different parts of the body may appear unrelated. Genomic information can provide additional context by helping explore whether some symptoms may share an underlying genetic connection.
Your genome may add context
Genetic information may provide additional context for why certain symptoms occur together or why people experience similar conditions differently.
One broader genomic dataset
Whole-genome sequencing examines more genomic information than many targeted tests and creates a dataset that may support future review.
Better questions for your care team
Educational genomic insights can help individuals and families prepare more informed questions for physicians, genetic counselors, and other qualified professionals.
Many Conditions. One Deeper Look.
Explore possible genetic connections behind complex symptoms.
Symptoms can cross body systems and may not fit neatly into one category. EvaGenomics is designed to explore possible genetic connections across complex, overlapping, or persistent health concerns.
Autism and Neurodevelopmental Conditions
An autism diagnosis can answer what is happening, but families may still have questions about why it is happening and whether other health concerns may be connected. EvaGenomics explores genetic factors that may contribute to autism, developmental differences, intellectual disability, seizures, and related health concerns.
Neurological Conditions
Migraines, seizures, movement differences, neuropathy, weakness, and other neurological symptoms.
Metabolic and Mitochondrial Conditions
Fatigue, exercise intolerance, growth concerns, energy-production differences, and multi-system symptoms.
Autoimmune Conditions
Autoimmune and inflammatory symptoms may overlap across several body systems. EvaGenomics explores whether genomic information may add context to immune dysregulation, inflammation, or conditions that can be difficult to distinguish.
Cardiovascular Concerns
Heart rhythm differences, cardiomyopathy, blood vessel concerns, and other potentially inherited cardiovascular symptoms.
These categories are educational examples. Whole-genome sequencing does not guarantee a finding or diagnosis and may not be appropriate for every individual or health concern.
Other Complex Symptoms
Persistent, overlapping, or unexplained symptoms that do not fit into one clear category.
How EvaGenomics Works
A clearer way to explore your symptoms and genome.
Share Your Symptoms
Complete a guided questionnaire that helps organize your health history, symptom patterns, and current concerns.
Provide a Saliva Sample
After required ordering and eligibility steps are completed, an at-home saliva sample may be collected for whole-genome sequencing through a qualified laboratory pathway.
Deep Analysis Connects the Information
Your genomic information is evaluated in relation to your reported symptoms and available scientific evidence. Relevant findings are reviewed and prioritized based on their possible connection to what you are experiencing.
Receive Educational Insights
Receive an understandable educational report, questions for your healthcare team, and resources that may help guide your next steps.
What You May Receive
Understand your information. Ask better questions. Take a more informed role in your health journey.
EvaGenomics is designed to turn complex genomic information into an educational report that supports more productive conversations with your doctor, genetic counselor, or other qualified professional.
A structured summary of your reported symptoms and body-system patterns
Educational genomic findings prioritized around those symptoms
Clear explanations of evidence, uncertainty, and report limitations
Personalized questions to discuss with your doctor or genetic counselor
Resources that may help you explore specialists, support, research, and education
Future reanalysis options, subject to availability and consent
Built to support informed participation
The goal is not to tell you what to do. It is to help you understand what you have, know what to ask, and feel more empowered in your healthcare conversations.
Your report is educational and is not a diagnosis or treatment recommendation.
Why EvaGenomics
A symptom-driven approach to whole-genome information.
Starts with your symptoms
We organize what you are experiencing before reviewing genomic information.
Designed for future reanalysis
Genomic information may be reviewed again as new symptoms emerge or scientific knowledge develops.
Whole genome, not one narrow question
Whole-genome sequencing provides a broader dataset than many single-gene or condition-specific tests.
Understandable educational reports
Information is presented in clear language with uncertainty and limitations explained.
Symptom-Driven Deep Analysis
Specialized genomic analysis and interpretation tools help evaluate genomic information in relation to reported symptoms and available scientific evidence.
Privacy and meaningful consent
Users should understand how their information is collected, stored, shared, and used.
One Genome. More Than One Question.
Your DNA generally remains the same, but your symptoms, questions, and scientific knowledge can change. With your permission and subject to service availability, EvaGenomics may allow you to request reanalysis without repeating whole-genome sequencing.
New discoveries. New questions. New ways to explore your genomic information.
Step 1
Initial Analysis
Later
Reanalysis for New Symptoms
Over time
Reanalysis as Science Advances
Built for Complex, Real Lives
For people whose symptoms have never fit neatly into one box.
Individuals and families with unexplained or overlapping symptoms
Families seeking broader genetic context after an autism diagnosis
People exploring autoimmune, inflammatory, or multi-system concerns
Individuals who previously received negative, uncertain, or limited genetic test results
People who want to understand their information and participate more actively in healthcare conversations
EvaGenomics will not be appropriate for every individual or every health concern.
Privacy, Choice, and Transparency
Your genetic information is deeply personal.
Privacy, transparency, and meaningful consent must be part of every step.
Privacy by Design
Privacy and consent are considered throughout the experience.
Your Choice
You decide who receives your report and how you choose to share it.
Data Control
You may have options to request deletion of stored information or destruction of remaining samples, subject to legal, laboratory, and record-retention requirements.
Transparent Data Use
Information is used according to the permissions described in the applicable consent documents, Privacy Policy, and Terms.
Science First
Evidence, uncertainty, and limitations are communicated clearly.
Early Access
Your Symptoms Deserve a Deeper Look.
Join early access to learn when testing becomes available, receive product updates, and help shape the future of EvaGenomics.