BIOMARKERS × MACHINE LEARNING

Earlier
changes
everything.

We bring blood biomarkers and machine learning together to look for cancer earlier. VarSee Lung is our first product, available for research use.

Can I take the test? Ask about availability
One drop of blood, many signalsA blood drop drawn in fine indigo contour lines holds many small protein particles. As the page scrolls they line up into rows, read together, around a single point of gold light.
+One blood draw.
Many proteins, read together.
VarSee LungAvailable for research use
Scroll to follow the signal PUNE, INDIA · A GLOBAL AMBITION
New investors · October 2026

A warm welcome to

Anand Deshpande andSonali Anand Deshpande

They join us as investors, backing our work on turning blood biomarkers into actionable cancer intelligence using advanced machine learning.

Read the announcement
Four people wearing lanyards stand together against a dark background.
Supported by
  • SEED, IISER Pune
  • Venture Center
  • Blockchain for Impact
  • Department of Science & Technology and Science and Technology Park, Pune
  • AIC-Pinnacle Entrepreneurship Forum
  • Hindustan Petroleum
  • Startup India
  • DST NIDHI
RESEARCH PROGRESS

From the lab to independent evaluation.

424 people

Across three lung-model cohorts

Including an independent evaluation at Tata Memorial Hospital.

Read the evidence summary

3 hospitals

Multicentre study ethics approval

For a VarSee Lung diagnostic accuracy study at Tata Memorial Centre sites.

See the study collaborations
Follow the signal
THE BIOMARKIQ APPROACH01 / 03
Biological signals

A signal is a start.

Blood carries proteins that change when a cancer starts to grow. One biomarker gives one view of that change.

Start with the biology

A panel sees more.

Cancer leaves more than one kind of clue. A panel measures several biomarkers at once, so the pattern between them can be read.

Explore the panel approach

Specialists connect it.

Specialist models each read the panel for one cancer. A gating model weighs them, with the person’s context, into one result.

Meet the MoE engine

One marker.
Part of the story.

Some biomarkers catch more cancers. Others clear more people without cancer. Watch what a second signal reveals in the same group of samples.

Why complementarity matters
How a signal is judged
FIRST SIGNAL →SECOND SIGNAL →THRESHOLD

Find people with the condition.

Of the people with the condition, how many does the test find? Everyone past the threshold is flagged; squares short of it are missed.

Identify people without it.

Of the people without the condition, how many does the test correctly clear? Circles past the threshold become false alarms.

Add a second signal.

A second measurement can pull the groups apart, so fewer are missed and fewer are flagged by mistake. Whether a real panel does this is what validation has to show.

Different experts.
Read together.

Each specialist model reads the panel for one cancer. A gating layer weighs their answers with the person’s context, so one result reflects the whole pattern.

  1. Inputs
    Protein panel
    Clinical contextAge, sex, smoking, recent blood count
  2. Specialists
    • Lung
    • Breast
    • Liver
    • Colorectal
    • Healthy baseline
  3. GateWeighs every reading with the person’s context
  4. One resultFor example: signal, likely lungor indeterminate, with a next step

One blood draw, many measurements.

A panel of proteins is measured from a single sample, alongside routine clinical context: age, sex, smoking and a recent blood count.

A specialist for each cancer.

Each specialist model is trained on the proteins relevant to one organ, and a healthy-baseline specialist reads what normal looks like. Each returns its own reading.

A gate weighs them, in context.

A gating model weighs every specialist’s reading together with the person’s clinical context, so no single signal decides on its own.

One result, or a next step.

The output is one result with its likely tissue of origin. When the readings disagree, it is indeterminate, with a directed next step instead of a forced call.

Lung first.
More cancers to follow.

Multi-cancer detection is the goal. We get there one cancer at a time, and lung comes first.

MEET OUR FIRST PRODUCT

VarSee Lung

A blood panel and a specialist model built around the biology of lung cancer. A multicentre study has ethics approval at three Tata Memorial Centre hospitals.

For research use onlyExplore VarSee Lung
A branching pattern. An early signal.An original leaf-inspired illustration. As you scroll, fine branches draw outward and a gold point follows the central stem.LOOK CLOSER.FOLLOW THE PATTERN.
BioMarkIQ VarSee — the leaf mark

Life leaves a pattern.
We’re learning to read it earlier.

LUNG CANCER / PROGRAM 01
THE NEXT HORIZONMulti-cancer. Built from the ground up.

Finding cancer matters.
False alarms matter too.

Detecting more cancers matters. So does avoiding unnecessary alarms. We study both, disease by disease.

BioMarkIQ’s three co-founders together in the laboratoryFROM THE BIOMARKIQ LAB

Cancer biology.
Machine learning.
One team.

Manasi, Snahlata, and Atharva founded BioMarkIQ to bring cancer biology and computational thinking into the same lab.

Today a team of ten works on the panels, the models and the studies.

Meet the team

Next for VarSee Lung: a study across three Tata Memorial Centre hospitals.

FOLLOW THE EARLY SIGNAL

Interested in the test?
Help build what comes next?

Ask about VarSee Lung, research partnerships, or investing in BioMarkIQ.

Ask about the test For investors