NextSeq 1000/2000 - Longer Reads and Extended Informatics
Explore key updates and features of NextSeq™ 1000/2000 sequencers and DRAGEN Bio-IT platform, focusing on longer reads and enhanced informatics capabilities.
Insights into Cancer Genomics via COSMIC v98
Explore cancer genomics through COSMIC v98, learning about new cancer genes, download files, IDs, and data improvements in this comprehensive overview.
Unraveling the Charge Heterogeneity of Biotherapeutics: icIEF Fractionation for Mass Spectrometry
Explore icIEF fractionation for mass spectrometry in biotherapeutics, focusing on charge heterogeneity profiling and its importance as a critical quality attribute in drug development.
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.
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.
Novel Bioassays in Picodroplets for Single-Cell Analysis
Explore microfluidic devices for high-throughput bioassays using picodroplets as miniaturized test tubes, revolutionizing drug discovery and preclinical development with efficient single-cell analysis techniques.
Node-Pore-Sensing: A Versatile Method to Phenotype Cells
Explore Node-Pore Sensing, an innovative electronic method for cell phenotyping. Learn how this technique measures cell properties and distinguishes sublineages in human mammary epithelial cells.
Linking Single-Cell Function to Multi-omic Analysis Using 'Lab on a Particle' Technology
Explore innovative 'Lab on a Particle' technology for single-cell analysis, linking cell function to multi-omic data. Learn about hydrogel microparticles for cell capture and secretion analysis in various applications.
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.
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.
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.
Overcome a "Big" Challenge: Progress on Mass Spectrometric Analysis of Large Molecules
Explore advancements in mass spectrometric analysis of large molecules for clinical applications. Learn key components, recent progress, and resources for efficient protein quantitation in clinical laboratories.
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.
Monitoring Intact Light Chain of Therapeutic Monoclonal Antibodies in Human Serum by LC-MS for Clinical Research
Explore intact light chain quantitation for measuring therapeutic mAb concentrations in human serum using Orbitrap Exploris 240 MS. Learn about simplified workflows and solutions for challenging mAbs.
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.
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.
Sequencing Errors and Alternative DNA Structures
Explore how non-B DNA structures affect sequencing errors across Illumina, PacBio HiFi, and Oxford Nanopore technologies, and learn their implications for genomic studies.