Backed by Y Combinator

Mapping cancer biology in real tissue.

We generate spatial, molecular, and functional maps from patient tumor samples so cancer biology can be studied in its native context.

01

Block Sourcing

FFPE tumor blocks sourced from hospital and biobank partners, with anonymized clinical annotations covering tumor type, grade, stage, and treatment history.

02

Sectioning

Blocks are sectioned onto spatial capture substrates and quality-controlled, preserving native tissue architecture and spatial coordinates.

03

Spatial Profiling

Spatial transcriptomics paired with imaging-based morphology (H&E and immunofluorescence), with every measurement anchored to its location in the tissue.

04

Tissue Maps

Spatially resolved maps of cell states, programs, and niches that show how each tumor is organized across patient cohorts.

01

Live Tissue Sourcing

Fresh tumor resections and live tissue, with the option to harvest dissociated single cells, sourced from clinical partners under matched clinical annotations.

02

Slicing & Perturbation

Fresh tumors are processed into precision-cut tumor slices, or dissociated cells, and allocated into matched untreated and perturbed arms.

03

Response Readouts

Perturbation-response readouts across arms, including transcriptomic, proteomic, and functional or viability assays measured after treatment in living tissue.

04

Response Profiles

Response profiles capturing how living tumors react to drugs and perturbations, including sensitive and resistant cell populations.

A tissue-first data and model engine for cancer biology.

Spatial Genomics

Spatial transcriptomics

Readouts from tumor blocks that map gene expression back onto tissue architecture, revealing neighborhoods, programs, and spatially organized disease states.

Tissue Phenotype

Morphology & proteomics

Histology, morphology, and protein-level measurements that anchor molecular findings in the physical structure of each patient sample.

Functional Response

Ex vivo perturbation

Precision-cut tumor slices exposed to drugs, cytokines, immune modulators, and genetic or molecular perturbations to observe response in native tissue.

Models

Multimodal AI models

Multimodal models trained on our proprietary sequencing and spatial transcriptomics data, supporting target discovery, perturbation-response prediction, cross-modal tasks such as inferring spatial expression from H&E imaging, and patient stratification.

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.