Next-Generation Sequencing (NGS) in Biomarker Discovery
Next-generation sequencing (NGS) has become indispensable in identifying and validating novel biomarkers across various diseases. This track explores how whole-genome, exome, and targeted sequencing techniques accelerate the detection of genetic alterations relevant to diagnostics and therapeutics. Presentations will cover variant calling, transcriptomic profiling, and bioinformatics pipelines for analyzing complex NGS datasets.
Further discussions will address standardization, cost reduction, and quality control challenges in clinical sequencing. Case studies demonstrating NGS applications in oncology, rare diseases, and pharmacogenomics will be presented. Attendees will learn how integrating NGS with other omics platforms enhances biomarker discovery and enables precision medicine at scale.
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