KromaTiD

KromaTiD

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Private Company

Total funding raised: $7.5M

Overview

KromaTiD has established itself as a specialized contract research organization (CRO) and lab focused exclusively on single-cell genomic visualization and analysis. The company's KROMASURE™ Platform utilizes advanced fluorescent hybridization technology to provide orthogonal confirmation for sequencing data, critical for IND submissions and batch release testing in cell and gene therapy development. By offering services from research through GLP/GMP-compliant testing, KromaTiD addresses the growing need for definitive genomic integrity data to ensure therapy safety and efficacy. Its business model is built on providing essential analytical services and platform data to biotech, pharma, and regulatory partners.

Genetics & Genomics

Technology Platform

KROMASURE™ Platform: A suite of advanced fluorescent in situ hybridization (FISH) and cytogenetic assays for single-cell visualization and analysis of genomic integrity, structural variants, and transgene mapping. It provides orthogonal, high-resolution data to complement next-generation sequencing.

Funding History

2
Total raised:$7.5M
Series A$5M
Seed$2.5M

Opportunities

The rapid growth of the cell and gene therapy sector creates massive demand for robust genomic safety data.
Increasing regulatory scrutiny on genomic stability positions KromaTiD's orthogonal visualization platform as a potential standard for IND submissions and batch release testing.

Risk Factors

Competition from evolving sequencing technologies that may offer cheaper or higher-throughput structural variant detection.
Dependency on the health of the broader cell and gene therapy market, which is subject to funding cycles and clinical setbacks.

Competitive Landscape

KromaTiD competes with broad-based CROs offering cytogenetic services and with genomics companies advancing long-read sequencing and bioinformatic tools for structural variant detection. Its key differentiation is an exclusive focus on single-cell visualization, providing direct, unambiguous data that sequencing infers indirectly.