Genomics

Custom reagents for multiplex PCR assays may be the missing ingredients for your infectious disease panel

Join Today's Clinical Lab and Peter Hahn, PhD, to learn about advantages of and approaches to exome sequencing for rare disease identification

Watch this webinar to learn how you can design a workflow for effective analysis of cfDNA occurring with <1 percent variant allele frequency (VAF)

Maybe: The largest-ever analysis identifies over 3,500 genetic variants that influence tobacco and alcohol consumption

Download this white paper to learn how to make your WES workflow more robust and cost-efficient

Download this application note to learn how to easily generate diagnostics reports for rare cancers using a comprehensive database

Download this eBook to learn about clinical decision making for precision oncology using a curated, comprehensive database 

Download this infographic to learn about how you can perform whole exome sequencing (WES) at half the cost and in a third of the time

To make personalized medicine the standard of care, we will need to go beyond sequencing tumor DNA

QCI Interpret One provides labs with the best source of high-quality variant interpretation