Watch on-demand webinars discussing how ultrahighly sensitive and customizable targeted next-generation sequencing panels are applied in oncology and human genetic research.
Advances in NGS for Ultra-High Sensitivity Applications in Translational and Clinical Research
Speaker:
Dr. Hans Atli Dahl
Co-founder & Chief Technology Officer, Amplexa Genetics
In this webinar or event, we’ll discuss:
- A study that sought to test the hypothesis that causative genetic variants for inherited diseases that often fall into the category of “de novo mutations” are sometimes the result of undetected mosaicism in the parents.
- Details of how Ion AmpliSeq HD panel addresses the need for ultrahigh sensitive detection and its potential to deliver new insights about the causes of genetic diseases.
Rare allele detection in FFPE and cfDNA pathology research samples
Speaker:
Dr. Karl Kashofer
Head of the Laboratory for Diagnostic Genome Analysis, Department of Pathology, Medical University of Graz
In this webinar or event, we’ll discuss:
- Factors to consider when choosing a genetic analysis technology for pathology studies
- Data interpretation for rare allele detection in samples with large deletions
- How to optimize detection sensitivity in formalin fixed paraffin embedded (FFPE) and cell-free DNA samples
- Comparison of digital PCR, Ion AmpliSeq, Ion AmpliSeq HD and Oncomine cell-free DNA assays
