How Can You Streamline Your Whole Exome Sequencing Workflow?

For diseases whose underlying genetics are poorly understood, comprehensive next-generation sequencing methods such as whole exome sequencing (WES) can provide better insight. WES workflows are typically complex, time-consuming, and vary based on probe design, capture efficiency, and capture specificity. 

This white paper considers the three steps of WES workflows to save time and lower costs while delivering robust results:

1. Library preparation, such as with the QIAseq Library Kits (FX DNA; Ultralow Input)
2. Library enrichment, such as with the QIAseq Human Exome Kit
3. Sequencing and analysis