GeneReader NGS System (ROW) - Next-Generation Sequencing (NGS)

2 GeneReader NGS System Library Preparation Target Enrichment Nucleic Acid Extraction The application of Next-Generation Sequencing (NGS) technologies to clinical research is having a major impact on the identification of genetic variants that impact human health. NGS enables the study of multiple disease markers from a single sample in a single analysis, making it both faster and cheaper than traditional single gene analyses. Recent technological developments in instrumentation, consumables and bioinformatics have brought NGS to the benchtop and are enabling the clinical research community to find answers to many of the most challenging questions. NGS is helping to refine our understanding of disease and provide the potential to create better research tools. More actionable data and insights in one go. More confidence at one glance. A small step for you, a giant leap for your results. Next-Generation Sequencing (NGS)

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