The thesis · Drug discovery from India

India's genetic diversity is the next frontier for drug discovery.

We generate clinical-grade genomic data at the point of care, across 20+ hospitals in India, and link it to clinical outcomes. The result is the population-scale, clinico-genomic resource that drug discovery has been missing.

1
Read
2
Link
3
Cohort
4
Discover
Genome readoutInterpreted
Rare variantBRCA1 c.68_69delPathogenic
Polygenic riskBreast cancer · top 4%
PharmacogenomicsCYP2D6 · poor metabolizer
AncestrySouth Asian · under-catalogued
02 · Link
Sequence, joined to the outcome.
Genome
BRCA1+ · pathogenic
Clinical record
Ca. breast · responded
Linked patient
Genome ⋈ record · outcome-grade
03 · Cohort
One patient becomes a population.
Genotype +Phenotype +
0
deeply-phenotyped patients · cohort assembled
04 · Discover
The cohort reveals a new target.
Genome-wide significance
Target found
GENE-7q21
genome-wide significant · novel
Closing the loop
From target to candidate therapy.
Target
GENE-7q21
genome-wide significant
Candidate
WLY-0312
druggable · in-silico hit
Trial
Phase II
matched, phenotyped cohort

Sequence linked to phenotype and outcome: one record that compounds in value with every patient.

15,000+

clinical records, linked at the point of care

1,000+

with genomic data, compounding

20+

hospital sites across India

Why now

The diversity the world's biobanks miss, generated where care happens.

Sequencing is cheap; linked, ancestrally distinct data is not. India is where that data lives: 1.4 billion people and 4,600+ endogamous communities whose biology no European cohort can show. We generate it at the point of care, already linked to outcomes, and targets with that kind of human-genetic support are roughly twice as likely to clear the clinic.

On-demand testing

From a single panel to whole genomes at cohort scale.

Every assay you need, run on one reproducible pipeline.

Who we serve

One genomic backbone, every kind of partner.

Hospitals, prevention clinics, fertility centres, diagnostics labs, pharma and research teams, each starts from the same genomic backbone.

One company · two engines

Sequence linked to outcomes turns a cohort into a discovery engine.

Every patient we test deepens the resource: one clinical engine feeding a discovery engine, both on Health Hub, the same platform as the clinical agents.

Point of care
Clinical
Structured record
Every encounter
Genomic cohort
Discovery
+0
Drug discovery
Targets & therapies
The flywheel
Every patient
deepens the resource.
From the point of care to discovery — and back.

Same standards as the clinic

HIPAA

GDPR

SOC 2 Type II

ISO 27001

FHIR R4