Next Generation Sequencing (NGS) analysis is a relatively new and complex method of molecular diagnostic testing, but one that is growing rapidly in popularity. It has the potential to significantly increase standards of care through “personalized medicine,” or customized disease treatment based on an individual’s particular genes or the mutant genes present in a tumor.
Genomic and transcriptomic testing can already be used to rapidly diagnose infectious diseases like COVID-19, cardiovascular and neurological diseases, hereditary genetic disorders and cancer. But today’s standard methods for DNA and RNA library preparation for NGS involve a complex and time-consuming multi-step workflow with a high cost per sample.