Partnering & Collaboration

We collaborate with research institutions and industry partners on publicly funded ctDNA research.

Rooted in research

LIQOMICS grew out of cancer research, and our diagnostics are the result of that work. We are actively engaged in publicly funded projects and open to new research collaborations.

OVARSENSE

Ovarian Cancer

Ovarian cancer is often diagnosed at an advanced stage. In the collaborative project OVARSENSE, we aim to develop a test in which a simple blood sample (liquid biopsy) is sufficient to detect ovarian cancer and potential recurrences during and after therapy (minimal residual disease, MRD) at an earlier stage, thereby enabling more targeted treatment of ovarian cancer.

Diagram: a liquid biopsy blood sample supports early detection (is there cancer?), therapy response monitoring (did the treatment work, is additional therapy needed?), and recurrence surveillance (is there residual disease, is the cancer likely to recur?) for ovarian cancer.
Funding Co-financed by the European Union and the Ministry of Economic Affairs, Industry, Climate Action and Energy of North Rhine-Westphalia (EFRE.NRW)
Cooperation Partners Logos of Miltenyi Biotec and Evangelisches Krankenhaus Bergisch Gladbach
Download Poster (PDF)

Project Consortium

Project Coordinator Liqomics GmbH Cologne, Germany
  • Gynäkologisches Krebszentrum, Evangelisches Krankenhaus Bergisch Gladbach gGmbH Bergisch Gladbach, Germany
  • Miltenyi Biotec B.V. & Co. KG Bergisch Gladbach, Germany

Project duration: January 2026 – ongoing

Project ID: IN-GE-3-020a

Project Title: Development of an ultrasensitive, non-invasive method for the early detection and determination of minimal residual disease (MRD) in ovarian cancer using circulating tumor DNA (ctDNA) in liquid biopsies.

Project Goal

A test that can both determine minimal residual disease, as well as being used for the early detection of ovarian cancer is under development. This minimally invasive method reduces the burden on patients and offers significantly higher accuracy than traditional methods.

Approach

The goal is to enable precise and personalized diagnostics through the analysis of circulating tumor DNA (ctDNA) using liquid biopsies and next-generation sequencing (NGS). This innovative technology allows for the early detection of recurrences and supports personalized therapy decisions.

FOCuS

Small Cell Lung Cancer

Small cell lung cancer (SCLC) is a type of tumor with an extremely low survival rate. In our collaborative project FOCuS, we aim to develop a new form of immune cell therapy together with a companion cancer test (liquid biopsy). The goal is to enable earlier, more targeted, and more effective treatment of SCLC through the combined development of therapy and diagnostic testing.

Diagram: the FOCuS approach flows from cancer diagnosis to treatment (CAR T-cell therapy) combined with monitoring (liquid biopsy) for small cell lung cancer.
Funding Co-financed by the European Union and the Ministry of Economic Affairs, Industry, Climate Action and Energy of North Rhine-Westphalia (EFRE.NRW)
Cooperation Partners Logos of Uniklinik Köln, LungCancerGroup Cologne, and Fraunhofer IZI-BB
Download Poster (PDF)

Project Consortium

Project Coordinator University Hospital Cologne (AöR) Cologne, Germany
  • Liqomics GmbH Cologne, Germany
  • Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Munich, Germany
  • Fraunhofer Institut für Zelltherapie und Immunologie, IZI Leipzig, Germany

Project duration: January 2026 – ongoing

Project ID: IN-GE-3-001b

Project title: FOCuS - Flüssigbiopsien und Optimierte CRISPR knock-in CAR T Zellen zur Behandlung des SCLC

Project Objective

The aim of the project is to develop a CAR T-cell therapy for the treatment of small cell lung cancer (SCLC).

Approach

We use non-viral genome editing with CRISPR/Cas9 for the targeted generation of optimized CKI CAR T cells. In addition, we are developing a liquid biopsy-based testing system that enables longitudinal molecular characterization of SCLC during therapy, including MRD monitoring and subtyping.

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