qPCR Research Testing for Pharmacogenomics: Workflow, Validation and Content Selection
Explore key components of Pharmacogenomics testing, including workflow, validation, and content selection for qPCR research in laboratory settings.
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.
Selective Neuronal Vulnerability in Neurodegeneration
Explore selective neuronal vulnerability in neurodegeneration, focusing on Spinocerebellar Ataxia type 1. Gain insights into cerebellar degeneration patterns and potential underlying mechanisms.
Spatial Mapping of Pain-Associated G-Protein Coupled Receptors and Biomarker Localization in Mouse Brain Using RNAscope HiPlex v2
Explore spatial mapping of pain-related GPCRs and biomarkers in mouse brain using advanced RNAscope HiPlex v2 and RNA-protein co-detection techniques for single-cell resolution gene expression analysis.
Automated Tools for Consistency, Reliability and Efficiency in Plasmid and Protein Purification
Explore automated tools for consistent, reliable, and efficient plasmid and protein purification, Western blotting, and cell isolation. Gain insights from industry expert Rouba Najjar.
Droplet Microfluidics in PCR: Technology and Applications
Explore droplet microfluidics in PCR, focusing on Digital Droplet PCR technology, its advantages over traditional qPCR, and applications in various fields like NIPT, pathogen detection, and liquid biopsy.
Live Single Cell Biology at Ultra-high Throughput for Applications in T Cell Potency and Small Molecule Drug Testing
Explore ultra-high throughput single cell biology for T cell potency and drug testing. Gain insights into CAR-T therapies, potency assays, and overcoming barriers in cell-based medicines.
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.
Improving Fetal Fraction of EDTA-Gel NIPS Samples Using Gel-Based Size-Selection
Explore gel-based size-selection techniques to enhance fetal fraction in EDTA-Gel NIPS samples, improving non-invasive prenatal screening accuracy and reliability.
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.
Recent Advances in Lyophilized qPCR Reagents
Explore recent advancements in lyophilized qPCR reagents and their impact on molecular diagnostics with insights from an industry expert.
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.
HIV-1 Genotyping Targeting Integrase - Perspectives on Surveillance of Antiretroviral Drug Resistance
Explore HIV-1 drug resistance surveillance, focusing on South Africa's efforts and a new genotyping kit targeting protease, reverse-transcriptase, and integrase inhibitors.
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.
Moving Beyond Mutation - AI-driven Functional Precision Medicine for Cancer
Explore AI-driven functional precision medicine for cancer, combining live-cell assays, immune profiling, and machine learning to predict drug efficacy and improve treatment outcomes.
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.
How Population-based Metrics for Diversity Shape Human Genomics Research and Reference Resources
Explore how population-based diversity metrics influence human genomics research and reference resources. Gain insights into the complexities of racial and ethnic classification in biomedical studies.
DNA Polymerases at Work: Finding Your PCR Champion
Explore DNA polymerase technology evolution and learn to select the optimal enzyme for your PCR applications, enhancing research efficiency and outcomes.
Improving Genomic Analysis by Fixing Reference Errors
Discover how to enhance genomic analysis by correcting GRCh38 reference errors, impacting variant calling in 33 protein-coding genes. Learn about FixItFelix for efficient re-analysis while maintaining existing annotations.