Backed by Y Combinator

Mapping cancer biology at scale.

We perturb real patient tumor tissue and study response at a molecular level.

From surgical resection to perturbation dataset.

01

Tissue Collection

Patient-derived tumor resections are collected from partner hospital networks. Tissue arrives with anonymized clinical annotations tumor type, grade, stage, and treatment history.

02

Precision Slicing

Fresh tissue is processed into precision-cut tumor slices. Unlike cell lines or organoids, PCTSs preserve the intact tumor microenvironment cellular composition, native spatial arrangement, and vasculature.

03

Perturbation

Slices are allocated into matched arms untreated and perturbed. Compounds screened include checkpoint inhibitors, chemotherapeutic agents, cytokines, and more.

04

Multimodal Readouts

Numerous slices allow running a variety of panels post perturbation. These include transcriptomic, proteomic, and histological assays.

05

AI Training and Applications

Foundation models trained on perturbation-response data. Applications include target identification, in-silico drug screening, patient stratification, and biomarker discovery. Each experiment feeds back into the next cycle, informing the next round of data collection and perturbations.

Dr. Manolis Kellis

Dr. Manolis Kellis

Professor of Computer Science, MIT · Broad Institute

Leads the MIT Computational Biology Group, focusing on genomics, epigenomics, and regulatory genomics.

Dr. Nicole Paulk

Dr. Nicole Paulk

Founder & CEO, Siren Biotechnology · UCSF

Leading expert in AAV gene therapy, advising Dyno Therapeutics, Astellas, and Metagenomi.

Dr. Rashid Bashir

Dr. Rashid Bashir

Dean, Grainger College of Engineering, UIUC

Pioneer in bio-nanotechnology, biosensors, and microfluidics. CZ Biohub Chicago advisory committee.