NGS

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

Download this eBook to learn about the role of expanded carrier screening (ECS) in today's clinical decision-making for reproductive health

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

Download this white paper on assessing nucleic acid quality with automated electrophoresis for successful viral sequencing/detection assays

QCI^® Interpret for Oncology is software that helps molecular pathologists interpret molecular data for clinical decision making

Latest joint consensus guideline authored by representatives from AMP and College of American Pathologists

NGS library preparation of monkeypox variants a response to growing demand for viral surveillance solutions

Comprehensive pathogen detection from a single plasma specimen

Working through challenges in adoption to deliver a better standard of care

Germline BRCA testing continues to be underutilized, even for people with commercial insurance