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
Introduction Understanding clinical variants in genomics isn’t just for specialists anymore—it’s a growing necessity across healthcare
Advancing NGS bioinformatics analysis in Precision Oncology in Europe through the Instand-NGS4P project 1.
Introduction Next-Generation Sequencing (NGS) is transforming disease diagnosis and treatment by enabling fast and precise genetic analysis.
Introduction Clinical diagnostics are essential in identifying and managing medical conditions. Among its many tools, genetic testing stands
Genomics is transforming the landscape of modern medicine, paving the way for personalized treatments and improved approaches to disease
Since 2021, omnomicsNGS has held the CE-IVD mark under the In Vitro Diagnostics Directive (IVDD 98/79/EC). Euformatics Quality Manager Ashwini
Maneuvering through the world of clinical bioinformatics tools for next generation sequencing (NGS) is complicated on its own but also because of