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GENOMIC SAMPLE INTEGRITY

Securing sample identity
in genomic medicine

HMGx Sample Tracking eliminates patient-sample mismatches in NGS workflows using a fast, orthogonal PCR-based verification — directly from whole blood.

No DNA extraction required

Compatible with existing NGS pipelines

Designed for clinical-grade reliability 

THE PROBLEM

A critical blind spot in genomic medicine

Next-generation sequencing is transforming precision medicine. But ensuring that genomic data matches the right patient remains a major — and largely invisible — challenge.

WHERE ERRORS OCCUR

- Sample collection

- Handling and transport

- Laboratory processing

- Data attribution and reporting

WHAT'S AT STAKE

- Incorrect or delayed diagnoses

- Inappropriate treatement decisions

- Serious patient safety events

- Regulatory and liability exposure

As genomic workflows scale, the need for robust, independent sample identity verification becomes critical — not optional.

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