Over the last decade, target enrichment has enabled researchers and clinicians to use next-generation sequencing (NGS) in a staggering variety of research areas and applications. Whether the research aim is whole-exome sequencing, or a focused small panel of genes, targeted sequencing can be used to quickly and easily identify variants of interest across a broad range of sample types.
Download this application note to learn how automated NGS library preparation improved efficiency while maintaining library quality.
