This comprehensive 5-day workshop bridges the gap between wet-lab preparation and bioinformatics analysis in next-generation sequencing (NGS). Participants will learn the full workflow from library preparation and quality control to data analysis and biological interpretation.
Hands-on sessions include sample prep, size selection, and a live demonstration of an Illumina sequencing run. On the computational side, participants will explore quality assessment, basic read mapping, and data visualization.
This course is ideal for life science researchers looking to integrate sequencing into their projects or better understand NGS datasets.
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