top of page

WHEN  EVERY  CELL  MATTERS

Identify cancer cells
that survive treatment.

Target the ones that
drive relapse.

SingleCell Biotechnology's functional assay platform identifies and profiles the rare subpopulations of tumor cells responsible for cancer recurrence — at single-cell resolution.

Microscopic Cell Clusters

1%

of tumor cells survive treatment and cause relapse

These outliers drive every relapse — and are invisible to current tools.

> 90%

of new cancer drugs fail in development

Most were never tested against the cells that survive treatment.

01

THE FLAW

Current methods measure the average — not what matters

Standard drug efficacy assays rely on population-level readouts — averaging the growth and survival behavior of millions of cells. This approach only works when the population is homogeneous and behaves as one.

​

02

THE BIOLOGY

Cancer is one of the most heterogeneous systems in biology

Within a single tumor, cells behave differently, respond differently, and survive differently. Averaging across them doesn't just miss the outliers that drive relapse — it actively hides them.

​

03

THE CONSEQUENCE

The survivors are invisible — until they drive relapse

The ~1% of cells that resist treatment are statistical outliers in the distribution. Population-level assays report them as noise. They are not noise - they are the disease.

​

04

THE REQUIREMENT

Fighting heterogeneity requires looking at every cell individually

A different approach is needed — one that sees the full distribution, not just the average, and focuses on the surviving outliers to unmask what population-level methods conceal.

​

05

OUR ANSWER

A platform to unmask single-cell heterogeneity at precision and scale

Measure every cell individually — capturing the full distribution of behavior across thousands of single cells per experiment — so the outliers that drive relapse can no longer hide.

​

Meet the first platform built to track,
identify and profile the cells that survive treatment.

Our platform is built around three phenotypic assays that capture the hallmark behaviors of treatment-resistant tumor cells — the biological mechanisms directly responsible for cancer recurrence and mortality.

 

Each assay is designed for high-content, high-throughput data collection, enabling drug screening, target identification, and disease analysis at single-cell resolution.

PHENOTYPE 01

Clonogenicity

 

 

The ability of a tumor cell to proliferate continuously and regenerate a full colony — one surviving cell is enough to restart the disease.

​​​​

Tumor regeneration capacity

PHENOTYPE 02

Migration

The ability of a tumor cell to invade surrounding tissue and travel to distant sites in the body. This is the biological mechanism behind metastasis — the spread of cancer beyond the original tumor that makes it life-threatening.

Invasion and metastasis

PHENOTYPE 03

Dormancy

The ability of a tumor cell to remain alive but non-dividing — evading both treatment and detection. Dormant cells can persist silently for months, making cancer appear cured when it is not.

​

Silent persistence and late relapse

PLATFORM COMPONENTS

flowchart_1.png

Microwell Plate

Captures clonogenicity and dormancy simultaneously at ~3,000 single-cell datapoints per well.

flowchart_2.png

Microchannel Plate

Captures cells in 3D migration state to analyze speed, invasion, and morphological changes at ~400 cells per well.

From samples to molecular target - in one integrated platform.

01

SAMPLES

Cells derived from a patient biopsy or patient-derived xenograft (PDX) model are prepared and loaded into the assay platform. Compatible with glioblastoma, breast cancer, and other solid tumors.

02

IMAGE DATA ACQUISITION

Cells are imaged over time across the microwell and microchannel array plates, generating high-content image data at single-cell resolution. Compatible with standard 96-well plate imaging systems.

03

IDENTIFYING TREATMENT RESISTANT SURVIVORS

Our machine learning and computer vision based automatic image analysis pipeline classifies every cell's behavior across thousands of spatially indexed positions — distinguishing dormant survivors, clonogenic outliers, and migrating cells from the majority that respond to treatment. 

04

PRECISION RECOVERY OF CELLS OF INTEREST

Using spatial coordinates generated by the analysis pipeline, cells in specific outcome categories are extracted directly from the plate — enabling downstream molecular analysis of precisely the cells that survived treatment.

05

FROM PHENOTYPE TO MOLECULAR TARGET

Recovered cells undergo multi-omic profiling on standard platforms such as Parse Biosciences or Illumina, linking each cell's phenotypic behavior directly to its molecular state. The result is a per-patient resistance map — connecting dormancy, clonogenicity, and migration to the molecular targets that drive them

The Team

Karoliina Stefanius, PhD

President

Bryan Presley

Co-Founder & Director of Engineering

Shiska Raut, M.S.

Machine Learning & Computer Vision Engineer

Board of Directors

Azam Anwar, MD

Chairman & Co-Founder

Douglas Krohn, MD

Chief Medical Officer

Matthew Head

Board Member

Scientific Advisors

Digant Davé, PhD

Co-Founder & Scientific Advisor

Core IP Inventor, Professor, UT Arlington

Robert Bachoo, MD, PhD

Co-Founder & Scientific Advisor

Core IP Inventor, Neuro-Oncologist, UT Southwestern Medical Center

Elizabeth Maher, MD, PhD

Co-Founder & Scientific Advisor

Neuro-Oncologist, UT Southwestern Medical Center

News &
Traction

2022

Company Founded

Launched at BioLabs, Pegasus Park. Licensed core technology from UT Southwestern Medical Center.

Nov 2023

$2.5M CPRIT Grant Awarded

One of 6 companies selected from 95 applicants. Funds platform optimization for GBM drug development.

Learn more

Mar 2026

Reproducibility Data Published

Reproducibility data for the clonogenic assay published as a preprint on bioRxiv — demonstrating consistent single-cell measurements across experimental replicates.

Learn more

Apr 2026

Data Presented @ AACR 2026

Platform demonstrated high-throughput single-cell assay linking clonal growth phenotypes to molecular profiles across multiple GBM models.

Learn more

Partnerships

Work with Us

We are actively seeking partnerships with pharma companies, CROs, and research organizations focused on developing more effective treatments for cancer and cancer recurrence. If any of the following describes you, we want to hear from you.

Drug

Discovery

&

Target

Identification

CRO

Services

&

Drug

Candidate

Validation

Research

Collaborations &

Academic

Partnerships

Partners

Bio North Texas Logo
BioLabs Pegasus Park Logo
UT Southwestern Medical Center Logo

CONTACT US

Thanks for submitting!

Connect with us on Linkedin

  • LinkedIn

SingleCell Biotechnology, Inc.

3060 Pegasus Park Dr.
Dallas, TX 75247
Pegasus Park — Biotech Hub of Dallas

Contact Us

Unmasking heterogeneity. One cell at a time.

© 2026 by SingleCell Biotechnology, Inc.

bottom of page