CNVs in clinical diagnostics
Breakends, structural variants and CNV detection Copy number variants (CNVs) are the subject of extensive research. They are common features of
Driving Clinical NGS Success in Poland: A Partnership That Delivers Results
Executive Summary Euformatics and Analityk Genetyka have collaborated successfully on the Polish market to sign several hospitals as Genomics Hub
A Simplified Approach to Somatic Analysis in NGS
Introduction Analyzing somatic variants in next-generation sequencing (NGS) data can be complex. Between data preprocessing, variant calling,
How NGS Automation Improves Library Preparation Efficiency and Accuracy
Introduction Next-Generation Sequencing (NGS) demands precision and efficiency, but manual library preparation introduces variability and
A Guide to IVDR Requirements for Subsidiaries and Subcontracting: Key Aspects Explained
Introduction Understanding the regulatory requirements for subsidiaries and subcontracting under the In Vitro Diagnostic Regulation (IVDR) is
A Practical Guide to Clinical Variant Interpretation
Introduction Understanding clinical variants in genomics isn’t just for specialists anymore—it’s a growing necessity across healthcare
Transforming Cancer Care: The EU-Onco-Platform Reporting Solution
Advancing NGS bioinformatics analysis in Precision Oncology in Europe through the Instand-NGS4P project 1.