Partner for CE-IVD clinical NGS
4bases
CE-IVD NGS kits for oncology and inherited disease, with matched analysis software and reporting.
4bases4bases, based in Switzerland, makes ready-to-run CE-IVD NGS kits that take a diagnostic lab from sample to clinical report, with the bioinformatics included.
We supply 4bases oncology and hereditary-disease kits to hospital and reference labs in Pakistan, and source Oxford Nanopore sequencing kits through 4bases.
What we supply
Solid-tumour profiling
ONCO4B-IVD kits for actionable variants in solid tumours.
Hereditary cancer and HRD
BRaCA panels for BRCA1/2 and HRD pro for PARP-inhibitor eligibility.
Fusions and haematology
FUSION pro for gene fusions and HEMATO pro for haematological malignancies.
Inherited cardiac disease
CARDIO pro, a capture-based kit for familial cardiovascular diseases.
Analysis software
4eVAR variant interpretation and KaryoSolver for structural-variant analysis.
Oxford Nanopore kits
Nanopore sequencing kits supplied through 4bases.
News and Paper of the Month
4bases and Meridian Bioscience announce a collaboration on rapid NGS workflows
10 June 2026
Read ↗ReadingPaper of the Month, April 2026: ESC consensus on genetic counselling in dilated cardiomyopathy
Cardiogenetics
Read ↗ReadingPaper of the Month, March 2026: NGS in oncology, from genomic profiling to real-time disease management
Oncology
Read ↗ReadingNanopore sequencing moves towards clinical cytogenetics
Structural variants and karyotyping
Read ↗Product lines
- ONCO4B-IVD Solid-Tumour NGS Kits
- BRaCA Hereditary Breast & Ovarian Cancer Panels
- HRD pro (homologous recombination deficiency)
- FUSION pro (gene fusions)
- HEMATO pro (haematological malignancies)
- TP53 Panel
- CE-IVD Clinical NGS Panels
- Clinical Reporting & Bioinformatics
Planning a new assay or lab?
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