Longevity & Cellular Aging
How fast is your cellular ageing clock actually running?
Genes analyzed
$39 $59

Advanced Molecular Research
9528 Miramar Rd., Ste. 1155
San Diego, CA 92126
(619) 821-9429
Your DNA already holds the answers — we turn them into insight. Upload the raw file you already have from 23andMe, AncestryDNA, or MyHeritage and get a clear, pathway-level report on how your unique genetics may shape your biology. No new test. No blood draw. No guesswork.
DNA insight reports are personalized genetic analysis tools that decode the raw DNA data you've already uploaded to consumer testing services like 23andMe, AncestryDNA, or MyHeritage.
Instead of looking at isolated genes, our genetic pathway analysis examines how your variants work together across biological systems — influencing areas like energy metabolism, muscle growth, stress resilience, and cognitive performance.
Unlike clinical genetic testing (which requires a physician), NuGenia's reports are educational tools built for researchers, biohackers, and curious individuals. Each report is backed by peer-reviewed research, so you understand not just what your genetics may influence, but why.
Our approach differs from basic SNP (single-nucleotide polymorphism) reports because we analyze polygenic traits across entire biological pathways. That means a more complete picture of how your genetics may influence your health, performance, and well-being.
Upload the raw data file from any of these services — no repurchase, no waiting on a new kit.
Start with a single pathway from $29, or unlock every insight in the NuGenia Insights™ Master Report.
The panels are not all the same size — some pathways have four well-replicated markers behind them, others have fourteen — so the exact genes and a real sample result are published on every card below rather than hidden behind the buy button.
Uses the file you already have from 23andMe, AncestryDNA, MyHeritage or FamilyTreeDNA.
A versioned rule set, not a language model. Same file in, same report out.
Every score below is from a report we actually delivered — including the low ones.
How fast is your cellular ageing clock actually running?
Genes analyzed
$39 $59
Why does appetite and fat storage work differently for you?
Genes analyzed
$29 $49
What does your DNA say about focus, drive and pressure?
Genes analyzed
$29 $49
When are you built to sleep, and how well do you recover?
Genes analyzed
$29 $49
Where does your energy come from — and where does it go?
Genes analyzed
$29 $49
How does your muscle actually respond to training?
Genes analyzed
$29 $49
How well do you rebuild between sessions?
Genes analyzed
$29 $49
Where is your inflammatory set point?
Genes analyzed
$29 $49
How does your skin age, and how does it repair?
Genes analyzed
$29 $49
How are you built to hold up under pressure?
Genes analyzed
$29 $49
All fourteen pathways
The Master Report runs all fourteen pathways from a single upload and returns one overall alignment score alongside a per-pathway breakdown — so you see which pathways matter for you rather than choosing one in advance. It is the same engine and the same evidence standard as the focused reports.
Master Report · SKU RPT-MASTER
Sample result: 35/100 overall — foundational tier, published unedited like every other score on this page.
See the Master ReportCompare
Marker counts differ because the evidence differs, not because some reports are worth more. The price is the same either way, which is the point — there is no incentive to pad a panel. See which file formats we read →
| Report | Markers | Compounds | Genes analyzed | Sample | Price |
|---|---|---|---|---|---|
| Longevity & Cellular Aging | 7 | 3 | MTHFR · COMT · SOD2 · NQO1 · NNMT · TERT · KL | 27 | $39 |
| Weight Management | 8 | 7 | TCF7L2 · IRS1 · PPARG · FTO · CALCR · ADRB3 · PPARGC1A | 37 | $29 |
| Cognitive Performance | 4 | 4 | BDNF · COMT · DRD2/ANKK1 · MTNR1B | 46 | $29 |
| Sleep & Recovery Regulation | 6 | 7 | CLOCK · MTNR1B · SOD2 · MC3R · ACTN3 · COMT | 59 | $29 |
| Energy Metabolism | 6 | 7 | PPARGC1A · SOD2 · PPARG · ADRB2 · MTHFR · BDNF | 66 | $29 |
| Muscle Hypertrophy | 4 | 5 | MSTN · ACTN3 · IGF1 · IGF1R | 64 | $29 |
| Growth Hormone & Tissue Repair | 12 | 13 | IGF1R · IGF1 · GHRL · MSTN · ACTN3 · IL10 · SOD2 · GSTP1 · HFE · MC1R | 46 | $29 |
| Inflammation & Immune Modulation | 14 | 8 | IL6 · VDR · TNF · IL1B · TLR4 · FCGR2A · OXTR · SLC15A1 · MC1R · MC4R | 43 | $29 |
| Skin Health & Regeneration | 4 | 5 | IL10 · GSTP1 · TERT · HFE | 46 | $29 |
| Mood & Stress Resilience | 5 | 4 | COMT · OXTR · BDNF · CLOCK · MTNR1B | 34 | $29 |
“Sample” is the peptide-relevance score from a real delivered report for that pathway. Low scores are common and are not a deficiency — they usually mean your own biology in that pathway is already doing its job. See a complete sample report →
Not sure where to start?
The right DNA insight report depends on your research goals and budget — and on whether you want one pathway in depth or all fourteen at once.
Pick the pathway that matches it. Studying genetics and athletic performance? Muscle Hypertrophy focuses exclusively on muscle-growth and recovery pathways. Researching metabolic optimization? Energy Metabolism examines your genetic influences on energy use and metabolic efficiency.
From $29one pathway · one-time payment
The Master Report delivers comprehensive analysis across every biological pathway — ideal for researchers conducting multi-system analysis, anyone wanting a complete profile across health and performance domains, and those seeking to understand their entire genetic architecture at the pathway level.
$79$129all fourteen pathways
All ten focused reports
Most people start with a single focus report to explore one area of interest, then upgrade to the Master Report for the full picture. All reports are delivered within minutes of your file being received — with no new DNA test required and complete privacy throughout the process.
You already did the hard part. We handle the science.
Export the raw data file from 23andMe, AncestryDNA, or another service and upload it securely — it takes about two minutes.
→Our engine analyzes your variants across biological pathways — not just isolated genes — to build a personalized, research-based picture.
→Your report is generated automatically and ready to download within minutes — clear, plain-English, and yours to revisit anytime.
The science
Understanding the science behind DNA insight reports helps you get more value from your genetic data. The difference comes down to one thing: whether variants are read alone, or read together.
Each SNP is read on its own and reported as a standalone trait. Informative — but it tells an incomplete story, because it cannot see how variants interact.
Take energy metabolism. It isn’t determined by a single gene — dozens of genes involved in mitochondrial function, thyroid regulation, and metabolic-enzyme production all work together. We map your variants across these interconnected systems.
Our research-backed methodology
we identify relevant genetic variants in your DNA file.
we analyze how those variants interact within known biological pathways.
we cross-reference each variant against peer-reviewed research.
we weight variants based on effect size and population data.
we convert complex genetic data into clear, usable insights.
This multi-step process is why our reports go deeper than basic SNP reports — and why they deliver significantly more meaningful, accurate insight. For anyone optimizing health and performance from genetic data, pathway-level analysis is the gold standard for turning raw DNA into real insight.
Your data
Genetic data is the most personal data you have. Here is exactly what happens to yours — and what never does.
Your raw DNA file is used for one thing — generating your report — and is erased from our systems as soon as processing finishes.
Files are encrypted in transit and at rest, and access is limited to the processing that produces your report.
We do not sell, rent, or share your genetic data with third parties — not with insurers, not with advertisers, not with researchers.
We do not build or retain a database of customer genomes. What remains after delivery is your report and your ordinary order record.
HIPAA-aligned safeguards. We hold your genetic data to the encryption, access-control and secure-disposal standards used for protected health information, because a raw DNA file deserves that level of care. To be precise about what that means: NuGenia Logics is a direct-to-consumer research and educational service, not a healthcare provider, and your insight report is not a medical record. Full detail is in our Privacy Policy.
We look at how variants work together across biological pathways — a far richer view than a single-gene readout.
Every insight is built on peer-reviewed research and clearly referenced, so you understand the "why" behind it.
Your genetic data is encrypted, never sold, and deletable on request. Your biology is yours alone.
Insight Reports connect naturally to our research peptide catalog, so your exploration is informed, not random.
Your data privacy isn't a feature — it's a commitment. We never sell your genetic information, we encrypt it end to end, and you can request deletion at any time. And if your report doesn't deliver clear, meaningful insight, our team will make it right.
Join the list for new report releases, genetics explainers, and research resources. No spam — unsubscribe anytime.