H. sapiens · 5,300 BP
Ötzi the Iceman
Copper Age · Ötztal Alps
Statistical modeling only. Non-clinical.
Our first product
Meet Haeckel.
Genomic infrastructure built to optimize and connect the human species across time. It holds the genotype, phenotype and extended phenotype of everyone in it, and resolves any single genome within.
It begins with one genome. Upload DNA in any format and a single pipeline resolves ancestry, health, pharmacology, phenotype, and lineage into one encrypted digital twin.
From there the twin can be optimized, simulated, and questioned in plain language. Push your biology to its limit, model the generations after you, trace the 100,000 years behind you.
At the scale of the species it becomes a network. Your genome connects you to the people alive who share it, to the genus Homo that came before you, and to the lineages that come after. Each person owns their twin and controls who can reach it. Mirror is how you enter Haeckel.
Mirror
LiveMirror AI · live demo
The model
Genotype · phenotype · extended phenotypeOne person. One Mirror. A species-wide network.
Consented exchange · the species
drag to rotate · tap a systemdrag to rotate · +/− to zoom · select a system
03 · Mirror
A natural-language interface to the genome.
Ask your genome in plain language. Mirror answers across ancestry, risk, phenotype, pharmacology, and optimization, then renders the explanation on canvas.
Voice · face capture · memory
1
encrypted digital twin
3
biological layers
04 · Optimize
Optimization of the living phenotype.
Labs, wearables, sleep, cognition, hormones, and body composition are read against the genome through the Deterministic Biological Knowledge Graph.
PGx safety gating · labs · wearables
7
DBKG levels
12
PGx genes called
05 · Networks
Find the people who share your DNA.
Haeckel connects consented genomes by ancestry, haplogroups, kinship, and goals. Ask for the people closest to a biological question.
AI candidate finder · kinship · goal matching
165
haplogroup nodes
2
consent tiers
06 · Lab
Polygenic modeling of offspring.
Two genomes combine into probabilistic offspring models across Mendelian inheritance and six independent polygenic score methods.
Projected traits · Mendelian inheritance
6
independent PRS methods
5
LD reference panels
07 · Origins
Ancestry inference and lineage reconstruction.
A 3D map of genetic history: 60+ populations, migration arcs across 100,000 years, and maternal and paternal lines traced to their roots.
Neanderthal measured · Y-DNA · mtDNA
60+
populations resolved
100K
years reconstructed
08 · Genome
22 analyzers over the raw variants.
Health risk across 89 genes. Phenotype, pharmacogenomics, nutrigenomics, HLA, CNV, ROH, and searchable SNP-level explanations.
HLA · CNV · ROH · searchable SNP explanations
22
analyzers in production
89
health-risk genes
Ancient DNA
Compare your DNA to the ancients we hold.
Real genomic profiles from peer-reviewed literature, placed on the same tree as you. Open Mirror with them and ask them anything.
H. sapiens · 3,330 BP
Tutankhamun
New Kingdom Egypt · Valley of the Kings
H. sapiens · 10,000 BP
Cheddar Man
Mesolithic Britain · Somerset, England
H. neanderthalensis · 44,000 BP
Vindija Neanderthal
Late Pleistocene · Croatia
H. neanderthalensis · 122,000 BP
Altai Neanderthal
Middle Pleistocene · Siberia
H. denisova · 76,000 BP
Denisova 3
Middle Pleistocene · Denisova Cave
In progress
+66
Pharaohs · Vikings · Andeans · Romans
73 enriched profiles now
Akbari 2026 dataset (10K+) integrating
Akbari 2026 dataset (10K+) integrating
The methods
Built on peer-reviewed science.
Every inference has a citation behind it, validated against the 1000 Genomes reference panel and the HGDP cohort before it reaches you.
01MLE-EM + Spatial thinning + Bootstrap WaldAncestry inference (significance-gated)
02PRS-CS · LDpred2 · Lassosum · SBayesR · C+TPolygenic risk scoring (six methods)
03S* statistic · ABBA-BABA D-stats · 4-state Viterbi HMMArchaic introgression (Neanderthal · Denisovan)
04HIrisPlex logistic regressionPhenotype prediction (eye · hair · skin · height)
05pgvector 1536-d OpenAI embeddingsNetworks · kinship · AI Candidate Finder
06Recursive phylogenetic traversal · Bayesian confidenceY-DNA + mtDNA haplogroup assignment (165 nodes)
07CPIC star-allele callingPharmacogenomics (12 genes · 10 FDA Black Box)
08KING-robust kinship · ROH detectionRelationship inference · consanguinity
09Evo 2 DNA foundation model (in integration)Variants of Uncertain Significance, first principles
Work with us
Join the next era of predictive genomics.
Heru Genomics is a network of exceptional people. Whether you work in science, AI, software, design, or medicine, if your talent moves this work forward, there is a place for you here.
Join the network01
The network
Scientists, AI researchers, engineers, designers, artists, clinicians. We invite exceptional people whose talent moves the work forward, and give them room to shape it.
02
Research & partners
Clinics, institutions, and researchers advancing genomic science with us, on methods, data, and validation.