bioRitma | 100% of Your DNA Turns Into Decisions.

Fitness & Performance

"Why am I always tired, even when I sleep enough?"

Heart & Circulation

"Why does caffeine affect me so differently?"

Brain & Mind

"Why do I feel anxious for no clear reason?"

Metabolism & Weight

"Why do some diets never seem to work for me?"

Fitness & Performance

"Why do I feel alert late at night but exhausted in the morning?"

Brain & Mind

"Why is it hard for me to focus, even when I'm motivated?"

Brain & Mind

"Why do my moods change more intensely than others'?"

Fitness & Performance

"Why do some workouts energize me while others completely drain me?"

Fitness & Performance

"Why am I always tired, even when I sleep enough?"

Heart & Circulation

"Why does caffeine affect me so differently?"

Brain & Mind

"Why do I feel anxious for no clear reason?"

Metabolism & Weight

"Why do some diets never seem to work for me?"

Fitness & Performance

"Why do I feel alert late at night but exhausted in the morning?"

Brain & Mind

"Why is it hard for me to focus, even when I'm motivated?"

Brain & Mind

"Why do my moods change more intensely than others'?"

Fitness & Performance

"Why do some workouts energize me while others completely drain me?"

Whole-genome Sequencing

Traits and health outcomes are shaped by many variants, interactions, and context across the genome. Looking at a small subset misses how these systems actually work.

Most consumer DNA tests

<1% of your DNA

100% of your DNA

Most DNA tests focus on incorrectly selected genetic markers. bioRitma uses whole-genome sequencing to evaluate both well-defined genetic conditions and everyday traits, with scientific depth and responsibility.

Explore bioRitma Academy

100%

of your DNA

Whole-genome sequencing
Compared to common genotyping-based tests

FAQ

Clear answers about what genome-driven health insights tell you — and where they stop.

We report tendencies — statistical predispositions toward traits or conditions — not diagnoses. A tendency is the average outcome among people who share your genetic pattern; it never replaces a doctor's judgment. A real medical diagnosis needs a clinician's evaluation, your family history, and often a confirmatory test in a clinical lab.

A polygenic risk score combines the small effects of many common genetic variants into a single estimate of how your genome compares with a reference population for things like cholesterol, diabetes risk, or heart-rhythm risk. It is relative, not absolute: a 'high' score means high relative to others — not a verdict, not a prediction of certainty.

Not yet. Most genetic risk research has been done on European populations, and accuracy drops in others. Where Turkish or regional data exists, we calibrate scores to it; where it doesn't yet, we flag the score as European-validated only in your report so you can read it with appropriate caution.

Each category focuses on an area of health: Skin & Beauty, Heart, Metabolism & Weight, Fitness & Performance, Brain & Mental Health, Endocrine & Fertility, Digestive & Urinary, Immunity & Allergy, Detox & Cellular Health, Longevity & Aging, Cancer Risk, and Child Health. Every category includes a curated set of reports built on whole-genome data.

Yes. We hold your full genome, not a small subset, so reports can be re-generated when new research becomes available — no new sample needed. If a previously unstudied variant becomes relevant to one of your reports, we update it and let you know in the app.

Yes. You can export both your raw and processed genetic files from the bioRitma app at no extra cost. It is your data — share it with a clinician, a researcher, or another platform if you want. We treat data portability as a basic right, not a premium feature.

No. bioRitma is informational, not a medical device. If a report shows something that genuinely matters clinically (for example, a likely-pathogenic variant in a major cancer or heart-disease gene), the report says so plainly and recommends confirmatory testing in an accredited lab with genetic counseling before any decision is made.

Your genome doesn't change, but how we frame your insights does. A moderate genetic tendency for high cholesterol reads very differently if your current lifestyle already keeps your levels healthy versus if it pushes them up. Your intake answers help us surface the most relevant guidance first.

Your data is kept on our own protected systems and never shared with third parties without your explicit consent. We comply with KVKK (Turkey's Personal Data Protection Law No. 6698) and apply GDPR-grade protections; genetic data is treated as a special category in both. You can export or delete your data at any time — once deletion is confirmed, your raw and derived files are removed from active and backup storage.

Systematic analysis of your whole genome.

Change starts with the right questions

At-home DNA kit

How It Works

1. Receive the kit.

2. Send your sample.

3. Explore your insights.

Your results. Clear, personal, always evolving.

Guidance, not diagnoses

DNA + lifestyle

Built for you, truly

Continuously updated

Choose the right genetic test package for you

Start with a bundle — pick the one that fits.

1 category

3-category bundle

5-category bundle

All 11 categories

Child Health

Skin Health & Beauty

Heart Health

Metabolism & Weight

Fitness & Performance

Brain & Mental Health

Endocrine System & Fertility

Digestive & Urinary System Health

Immunity & Allergy

Detox & Cellular Health

Potential Longevity & Aging

Cancer Risk

Child Health

Whole-genome Sequencing

On your phone

On your phone

Full-genome analysis, built for real use

Prioritize what matters

Connect genetics to daily life

Personalized, not generic

Focus on what affects you

Continuously updated

Check out our latest genomics research:

ECOLE: Learning to call copy number variants on whole exome sequencing data

An integrative framework for clinical diagnosis and knowledge discovery from exome sequencing data

Polishing copy number variant calls on exome sequencing data via deep learning

DORMAN: Database of Reconstructed MetAbolic Networks

Uncovering complementary sets of variants for predicting quantitative phenotypes

DeepND: Deep multitask learning of gene risk for comorbid neurodevelopmental disorders

ECOLE: Learning to call copy number variants on whole exome sequencing data

An integrative framework for clinical diagnosis and knowledge discovery from exome sequencing data

Polishing copy number variant calls on exome sequencing data via deep learning

DORMAN: Database of Reconstructed MetAbolic Networks

Uncovering complementary sets of variants for predicting quantitative phenotypes

DeepND: Deep multitask learning of gene risk for comorbid neurodevelopmental disorders

FAQ

Where your genetic insights come together.