Optimize yourself and your lineage to the edge of your genetic potential.

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22M+
SNPs
60+
Populations
100K
Years

Mirror AI · live demo

Statistical modeling only. Non-clinical.

The stack

One genome, read every way.

Haeckel reads one genome across optimization, ancestry, offspring modeling, and living DNA networks. Every layer works from the same encrypted twin.

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

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 · 7-level DBKG
HEART RATE64BPM↓ 4 vs yesterdaySLEEP SCORE827d avg 79STEPS8,427goal 10kOMEGA-3 INDEX9.4%optimalLOWOPTIMALHIGH

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 · two-tier consent
you81%89%94%12,847 KINDRED IN RANGE

Polygenic modeling of offspring.

Two genomes combine into probabilistic offspring models across Mendelian inheritance and six independent polygenic score methods.

6 PRS methods · projected traits
GENOME×GENOMEOFFSPRING · PROJECTEDEYE COLOR72%brownLACTOSE TOLERANT88%HEIGHT+1.4cmμAPOE RISKLOW

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.

60+ populations · 100K years · Neanderthal measured
PaleoGlobe with ancestry sidebar

22 analyzers over the raw variants.

Health risk across 89 genes. Phenotype, pharmacogenomics, nutrigenomics, HLA, CNV, ROH, and searchable SNP-level explanations.

22M+ variants · 89 genes · 10 FDA black-box alerts
VARIANT STREAMrs4988235LCTrs12913832HERC2rs671ALDH2rs3827760EDARrs11185098AMY1rs1426654SLC24A5rs429358APOErs7412APOErs4988235LCTrs12913832HERC2rs671ALDH2rs3827760EDARrs11185098AMY1rs1426654SLC24A5rs429358APOErs7412APOE
By the numbers
22M+
SNP reference database
60+
populations resolved
22
analyzers in production
6
polygenic risk methods
100K
years of migration
73
ancient genomes
Ancient DNA

Compare your DNA to the ancients we hold.

From Ötzi the Iceman and Tutankhamun to Cheddar Man, the Neanderthals of Vindija Cave, and the Denisovans of Siberia. Every profile carries real genomic data from peer-reviewed literature, and each one is placed on the same tree as you. Open Mirror with them and ask them anything.

Ötzi the Iceman — reconstruction
H. sapiens

Ötzi the Iceman

Copper Age

5,300 BPÖtztal Alps
Tutankhamun — reconstruction
H. sapiens

Tutankhamun

New Kingdom Egypt

3,330 BPValley of the Kings
Cheddar Man — reconstruction
H. sapiens

Cheddar Man

Mesolithic Britain

10,000 BPSomerset, England
Vindija Neanderthal — reconstruction
H. neanderthalensis

Vindija Neanderthal

Late Pleistocene

44,000 BPCroatia
Altai Neanderthal — reconstruction
H. neanderthalensis

Altai Neanderthal

Middle Pleistocene

122,000 BPSiberia
Denisova 3 — reconstruction
H. denisova

Denisova 3

Middle Pleistocene

76,000 BPDenisova Cave
In progress

+ 66 more

Pharaohs · Vikings · Andeans · Romans

Akbari 2026 dataset (10K+) integrating
The methods

Built on peer-reviewed science.

Every inference Haeckel makes has a citation behind it, validated against the 1000 Genomes reference panel and the HGDP cohort before it reaches you.

MLE-EM + Spatial thinning + Bootstrap Wald
Ancestry inference (significance-gated)
PRS-CS · LDpred2 · Lassosum · SBayesR · C+T
Polygenic risk scoring (six methods)
S* statistic · ABBA-BABA D-stats · 4-state Viterbi HMM
Archaic introgression (Neanderthal · Denisovan)
HIrisPlex logistic regression
Phenotype prediction (eye · hair · skin · height)
pgvector 1536-d OpenAI embeddings
Networks · kinship · AI Candidate Finder
Recursive phylogenetic traversal · Bayesian confidence
Y-DNA + mtDNA haplogroup assignment (165 nodes)
CPIC star-allele calling
Pharmacogenomics (12 genes · 10 FDA Black Box)
KING-robust kinship · ROH detection
Relationship inference · consanguinity
Evo 2 DNA foundation model (in integration)
Variants of Uncertain Significance, first principles
The invitation

All of this is live. Free to begin.

Upload your DNA. Compare yourself with the ancients we hold. Talk to Mirror about anything in your biology. The product evolves with the people who use it first.