Exome Sequencing
|2 min read
Labcorp Expands MRD Testing for Breast, Lung, and Colon Cancer Recurrence Risk
Labcorp MRD tests now monitor recurrence risk across stage I–III breast cancer, stage I–IIIA non-small cell lung cancer and stage III colon cancer
Updated |2 min read
New Mayo Clinic Technology Helps Solve the Unsolvable in Rare Disease Diagnoses
While manual reanalysis takes weeks, the new technology took from 10 seconds to 1.5 hours to reanalyze each unresolved case
|3 min read
Next Generation Sequencing Will Advance Newborn Screening
Genome sequencing uncovered risks of several pediatric-onset conditions that may benefit from early intervention
|3 min read
Exome Sequencing Identifies Patients with HBOC Missed by Current Screening Guidelines
Current guidelines ruled 60 percent of individuals identified with HBOC risk as ineligible for genetic testing
|1 min read
Save On Cost and Time Spent for Whole Exome Sequencing
Download this infographic to learn about how you can perform whole exome sequencing (WES) at half the cost and in a third of the timeSponsored by
|3 min read
Personalizing Precision Medicine through Comprehensive Genomic Profiling
To make personalized medicine the standard of care, we will need to go beyond sequencing tumor DNA
|2 min read
Solving Challenges in Exome Sequencing
New solutions provide more coverage in a cost-effective waySponsored by
|2 min read
Adopting NGS Technology for Routine Genetic Profiling
Working through challenges in adoption to deliver a better standard of careSponsored by
|4 min read
Reducing the Variability of Exome Sequencing
A look at interlaboratory variability of exome testing and ways labs can reduce this variability to improve patient care
|4 min read
The Benefits of Automating NGS Library Prep
Automating NGS library preparation can increase your lab’s throughput and accuracy while saving time and money
|5+ min read
Can Pharmacogenetic Testing Optimize Pain Management?
Harnessing the power of pharmacogenomics may make opioid analgesics safer and more effective
|1 min read
Study Supports Changing Secondary Genetic Findings Guidelines
When given a second chance, participants often change their minds about receiving secondary genetic findings
|5 min read
