AI-native precision oncology & drug discovery

From the whole genome to the right drug.

INNOONE turns whole-genome sequencing data into accurate diagnosis, optimal drug recommendation and new drug targets — one end-to-end AI platform, built by cancer-genomics researchers in South Korea.

InputWhole-genome & multi-omics data

WGS · RNA · proteomics · clinical records, pseudonymised at source.

InterpretDiagnosis & risk in days, not weeks

Germline and somatic variants, structural changes, cancer & disease risk scores.

ActOptimal drug & new targets

Matched existing therapies, dose guidance and structure-based drug-target discovery.

Two divisions, one End-to-End AI

Most tools stop at a report. INNOONE connects interpretation to therapy and to discovery, so the same genome that diagnoses a patient also points to the drug — and to the next drug.

Innoplatform · Diagnosis & prediction

Whole-genome interpretation for clinics and biobanks

Analysis, interpretation and reporting of WGS and multi-omics data — for cancer patients today and for the healthy population's lifetime risk.

  • INNOVANOME — multi-omics variant analysis: coding & non-coding, structural and copy-number changes, clonal evolution.
  • INNOPORTAL — clinical data browser and reporting for care teams.
  • INOME — personal genome platform: pharmacogenomic drug-safety card, hereditary risk, lifetime re-analysis.
  • INODE — pseudonymisation and federated analysis: the genome never leaves the institution.
Innodrug · Therapy & drug discovery

From a patient's mutations to the right molecule

AI-predicted protein structures and structure-similarity search turn genomic findings into treatment options and validated targets.

  • INNOVA — drug repurposing and optimal-therapy recommendation by protein-structure similarity, including dose and combination support.
  • INNODAC — antigen / antibody candidate discovery and cleavage-aware target refinement for antibody-drug conjugates (ADC).
  • Validated on 13 metalloprotease substrates · published in Scientific Reports (Nature Portfolio), 2026.

One blood draw, a lifetime of safer prescriptions

Health systems already pay for single-gene answers — DPYD testing before 5-FU chemotherapy is standard in Europe. We deliver the same certainty from the whole genome, for every actionable gene at once.

Tier 1

Drug-safety card

Full pharmacogenomic panel (DPYD, UGT1A1, NUDT15, HLA-B*58:01, CYP2C19, VKORC1 …) — definitive, immediate.

Tier 2

Silent hereditary risks

Familial hypercholesterolaemia, hereditary cancers (BRCA and beyond) — definitive, life-saving.

Tier 3

Family card

Carrier status passed to the next generation — definitive, inherited.

Tier 4

Risk scores & re-analysis

Cancer, dementia and metabolic onset risk scores, re-analysed every year as evidence grows.

Global by design

Data stays where it is. Only the analysis travels. Our pseudonymisation and federated-analysis module (INODE) lets hospitals and biobanks in Europe, the Americas and Asia use INNOONE without exporting a single genome.

Our European entry & Slush 2026 →

Slush 2026 · Helsinki · 18–19 Nov

Selected for the Gyeonggi Province AI Cluster Global Programme (Europe)

One of up to ten Korean AI companies selected to meet Nordic and European investors, hospitals and pharma. Read more ↗

Eight months since founding, proven by execution

Not an early-stage idea but an AI-native company inheriting twenty years of national genome research.

2,100+
Citations of the founding team's research — Nature, Nature Genetics, Cell and more
2
Core AI drug-discovery patents filed, under accelerated examination
4
Clinical proof-of-concept sites, including Korea's National Cancer Center and Big-5 hospitals
1
Peer-reviewed paper in Scientific Reports (Nature Portfolio), July 2026
Q1 2026

Incorporated in Seongnam · in-house GPU cluster (H100 · A100 · RTX 6000)

H1 2026

Two core patents filed · clinical PoC at four sites

Jul 2026

INNODAC paper published in Scientific Reports

Aug 2026

Gyeonggi Province AI Membership company

Nov 2026

Slush 2026, Helsinki — European PoC and investor talks

Company

INNOONE Inc. was founded in 2026 in Seongnam, South Korea, by cancer-genomics researchers and biotech operators whose work spans national genome programmes, Big-5 hospital validation and a KOSDAQ technology listing.

Science

National genome programmes

Founders have led genome analysis for Korea's national precision-medicine and bio-big-data initiatives and contribute to the ICGC-ARGO consortium.

Clinic

Validated where it matters

AI clinical-decision-support and data portals built with the National Cancer Center and leading university hospitals.

Capital

Operators, not only scientists

Leadership with venture-finance and public-listing experience, and a self-sustaining domestic health-check business funding global expansion.

Let's talk

Clinical or biobank partners, pharma collaborators and investors — we reply within two business days.

dwhong@innoone.org

Duncan Hong · Co-CEO

INNOONE Inc.
Seongnam-si, Gyeonggi-do 13590
Republic of Korea

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