From 50 to 500 Genes: How to Scale to Comprehensive Genomic Profiling While Reducing Cost, Time and Labor
Discover a workflow-agnostic software solution for scaling to comprehensive genomic profiling, reducing costs and time while leveraging a vast knowledge base for accelerated variant interpretation and patient-specific reporting.
Pharmacogenomics: Post COVID-19 Expansion of Molecular Testing
Explore the expansion of molecular testing post-COVID-19, focusing on RT-PCR applications in infectious diseases and pharmacogenomics. Learn about new opportunities in diagnostic technologies.
Targeted Sequencing of Large and Small Viruses
Explore targeted sequencing techniques for diverse viruses, from small to large genomes, with insights from UNC Vironomics Core Director Dr. Dirk Dittmer.
Ion AmpliSeq White Glove Service - Custom NGS Solutions for Infectious Disease Research
Explore custom NGS solutions for infectious disease research with Ion AmpliSeq White Glove Service, presented by Giorgio Pea from Thermo Fisher Scientific.
COVID and Beyond: NGS Applications for Public Health Surveillance, Epidemiology and Emerging Pathogens
Explore NGS applications in public health surveillance, epidemiology, and emerging challenges, focusing on COVID-19 and future preparedness.
Towards Newborn Screening by Whole Genome Sequencing
Explore the potential of whole genome sequencing for newborn screening with experts Thomas Defay and Stephen Kingsmore in this informative panel presentation.
Using NGS for MicroRNA and Gene Expression Analysis with Integrated Bioinformatics for Pathway Discovery and Biomarker Verification
Explore NGS techniques for microRNA and gene expression analysis, integrating bioinformatics for pathway discovery and biomarker verification in molecular biology research.
Precision Medicine as a Population Health Tactic
Explore precision medicine's role in population health with Dr. Howard McLeod. Gain insights on innovative healthcare approaches, implementation strategies, and policy implications from a renowned expert.
Curating the Genome to Drive Precision Diagnosis in Clinical Care
Explore genomic curation's role in precision diagnosis, enhancing clinical care through expert insights on cutting-edge techniques and applications.
PTS-ID: Developing Precision Behavioral Health Diagnostics for PTSD
Explore precision behavioral health diagnostics for PTSD with Dr. Tshaka Cunningham. Learn about genomics advancements, diversity in research, and innovative approaches to improve PTSD diagnosis and treatment.
KAPA HyperPETE - A Novel Primer Extension Target Enrichment Solution for Rapid and Reliable Variant Detection
Explore KAPA HyperPETE, a novel primer extension target enrichment solution for rapid and reliable variant detection in genomic research.
Using Gene Regulatory Networks to Understand Sex Differences
Explore gene regulatory networks and their role in understanding sex differences in health and disease through genomics and systems biology approaches.
HRD Evaluation and Scoring Using OncoScan CNV Assay - A Whole-Genome Microarray Research Solution
Explore HRD evaluation and scoring using OncoScan CNV Assay, a whole-genome microarray research solution for detecting genome-wide biomarkers in ovarian and breast cancers.
Development of a Novel Targeted NGS Panel for Analysis of DNA Methylation Biomarkers in Lung Cancer
Explore DNA methylation biomarkers in lung cancer through a novel targeted NGS panel, overcoming technical limitations for potential clinical applications in diagnosis and treatment.
HRD Evaluation and Scoring Using OncoScan CNV Assay - A Whole-Genome Microarray Research Solution
Explore HRD evaluation and scoring using OncoScan CNV Assay, a whole-genome microarray solution for cancer research, focusing on PARP inhibitors and synthetic lethality in tumors.
How to Translate Complex Genomic Data to Clinically-Oriented Personalized Cancer Care
Explore real-world application of translating complex genomic data into personalized cancer care, focusing on NGS testing and variant interpretation for hereditary cancers.
Towards A Global Federated System for Biosurveillance and Pandemic Early Warning Using Genomic, Epidemiological, Climate and Environmental Data
Explore a global federated system for biosurveillance using genomic, epidemiological, climate, and environmental data to model biological risks and enhance pandemic early warning capabilities.
The Advantage of Combining Short Read Whole Genome Sequencing, Optical Genome Mapping and Transcriptome Analysis in Constitutional and Cancer Diagnostics
Explore the benefits of combining short read whole genome sequencing, optical genome mapping, and transcriptome analysis for improved constitutional and cancer diagnostics.
Sequencing Single-Strand Mismatch and Damage Patterns by Long-Read Sequencing
Explore a novel long-read sequencing method for detecting single-strand DNA mismatches and damage, enabling new insights into mutation origins in healthy tissues and cancer.
Long-read Sequencing at Scale and High Accuracy
Explore long-read sequencing's advantages in genome analysis, focusing on accuracy improvements for complex genes and large-scale cohort studies in personalized medicine initiatives.
Precision Medicine as a Population Health Strategy
Explore precision medicine's impact on population health, from genomics in oncology to pharmacogenomics. Learn about broad sequencing panels and their potential to alter disease trajectories across populations.