Research Services

Our liquid biopsy solutions deliver precise circulating tumor DNA testing to support cancer research, therapy evaluation, and biomarker development.

Specialized ctDNA Analytics for Research and Development

Our liquid biopsy MRD solutions combine analytical precision with clinical expertise. The Vista platform enables highly sensitive MRD detection and circulating tumor DNA test applications, ensuring accurate therapy response monitoring and early relapse identification in research and clinical trials.

Vista Technology

Proprietary ctDNA analysis platform with exceptional sensitivity, detects very small amounts of tumor DNA

Clinical Expertise

Proven experience in clinical validation studies for lymphomas with significant prognostic results

Tailored Solutions

Customized assay development and study-specific adaptations for different tumor entities

Our Core Services

MRD Assays (Minimal Residual Disease)

Highly sensitive circulating tumor DNA detection for minimal residual disease (MRD) across multiple cancer types, enabling three-stage patient monitoring:

  • Genotyping to identify patient-specific mutations
  • MRD monitoring during and after therapy
  • Early relapse detection in follow-up care

Ideal for lymphomas and solid tumors.
Learn more about our liquid biopsy lymphomaresearch applications.

Custom Assay Development

Development of customized liquid biopsy diagnostics for specific research and clinical needs:

  • Tumor-specific gene panel development
  • Validation for new indications
  • Adaptation to study-specific requirements
  • Technical and analytical validation

Applicable for pharmaceutical, biotech, and academic research projects.

Clinical Study Support

Comprehensive support for all clinical study phases:

  • Study design and biomarker strategy
  • Regulatory consultation and documentation
  • Sample logistics and management
  • Data analysis and reporting

Applicable for Phase I–III studies and companion diagnostic programs.

Biomarker Discovery

Identification and validation of circulating tumor DNA biomarkers for translational and clinical research:

  • Prognostic and predictive biomarker discovery
  • Therapy response monitoring
  • Resistance mechanism identification
  • Combined biomarker panels development

Enabling breakthroughs in drug development and personalized medicine.

Research Focus Areas

Hematological Malignancies

Established Expertise: Clinically validated tests for B-cell lymphomas and Hodgkin lymphomas with proven prognostic significance.

LymphoVista: 326 samples, 88 patients - HR 4.61 for OS (p<0.0001)1
LymphoVista HL: HD21 Study - 4-year PFS 95.3% vs. 72.2% (p<0.0001)2

Solid Tumors

In Development: CancerVista for solid tumors with tumor-specific gene panels. Currently available for research use only (RUO).

Target indications include lung, breast, colorectal, prostate, ovarian, pancreatic cancers, and glioblastoma.

Collaboration Process

1

Needs Analysis

Define research goals, study design, and technical requirements.

2

Assay Development

Adapt or create Vista assays for your specific study.

3

Validation

Conduct technical and clinical validation per regulatory standards.

4

Implementation

Perform sample analysis, data evaluation, and provide ongoing project support.

Quality Standards & Regulation

LIQOMICS operates under strict quality assurance and international standards:

RiliBÄK-compliant

Quality assurance according to German regulations

ISO Standards

International laboratory quality compliance

GDPR-compliant

Secure and ethical data processing

Validated Reporting

All results undergo technical and medical validation

References

1 Schleifenbaum et al. Presentation at European Hematology Association (EHA) Annual Meeting 2024

2 Mattlener et al. Presentation at American Society of Hematology (ASH) Annual Meeting 2024

Start Your Research Project

Contact us for a non-binding consultation regarding your liquid biopsy diagnostics and circulating tumor DNA detection requirements.