Next-generation sequencing (NGS) has revolutionized biomedical research and has started to change the way clinicians diagnose and treat diseases, especially cancer and rare genetic disorders.
However, with the new applications of NGS, most notably single-cell RNA sequencing (scRNA-seq), new challenges arise and have to be addressed in order to ensure appropriate data quality and acquisition of interpretable results.
Download this guide to learn how to:
• Select the appropriate NGS method and sequencing platform
• Deal with samples of variable quality
• Set up and manage the data analysis pipeline