
Explore advanced human antibody discovery techniques using Beacon system and Harbour Mice® technology. Learn about single B cell cloning, NGS integration, and in-chip assays for efficient screening and diverse antibody development.

Explore next-generation sequencing with the Ion Torrent Genexus System and Oncomine Precision Assay. Learn about automated specimen-to-report workflow, performance, and data analysis in molecular testing labs.

Streamline somatic NGS analysis and reduce literature review time by 90% with the Human Somatic Mutation Database. Explore genomic content, clinical trials, and expert-curated insights for solid tumors and hematological malignancies.

Explore rapid next-generation sequencing innovations for faster, flexible DNA analysis in research and clinical applications, reducing turnaround time and improving cost-effectiveness.

Explore innovative gene therapy solutions, focusing on AAV plasmid DNA sequencing and synthesis for rAAV production, including ITR region management in clinical development.

Discover automated NGS library prep solutions to streamline workflows, reduce labor, and overcome adoption challenges. Learn about the AVENIO Edge System for efficient genomic research.

Explore the intersection of pathology and bioinformatics in next-generation curating for cancer genomics. Gain insights into best practices and advancements in clinical cancer genomic testing.

Explore NGS technologies' application in IVF, enhancing genetic screening and embryo selection for improved fertility outcomes.

Explore clinical NGS implementation at Holycross Cancer Center, focusing on challenges, solutions, and future directions in molecular diagnostics for cancer care.

Explore the versatility of Ion Torrent NGS systems for various applications, presented by Dr. Andy Felton, VP of Product Management & Market Development.

Explore molecular profiling of NSCLC samples using the Genexus turnkey NGS platform with Dr. Brendan Pang, a consultant pathologist and medical director.

Explore innovative approaches to developing next-generation biomarkers for cancer diagnosis and treatment, enhancing precision medicine and patient outcomes.

Explore a robust solution for SARS-CoV-2 detection and genetic variant surveillance using hybrid capture NGS assay and COVID-Dx. Learn about cutting-edge genomics tools for viral monitoring.

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.

Explore targeted sequencing techniques for diverse viruses, from small to large genomes, with insights from UNC Vironomics Core Director Dr. Dirk Dittmer.

Explore custom NGS solutions for infectious disease research with Ion AmpliSeq White Glove Service, presented by Giorgio Pea from Thermo Fisher Scientific.

Explore NGS applications in public health surveillance, epidemiology, and emerging challenges, focusing on COVID-19 and future preparedness.

Explore NGS techniques for microRNA and gene expression analysis, integrating bioinformatics for pathway discovery and biomarker verification in molecular biology research.

Explore genomic curation's role in precision diagnosis, enhancing clinical care through expert insights on cutting-edge techniques and applications.

Explore DNA methylation biomarkers in lung cancer through a novel targeted NGS panel, overcoming technical limitations for potential clinical applications in diagnosis and treatment.

Explore real-world application of translating complex genomic data into personalized cancer care, focusing on NGS testing and variant interpretation for hereditary cancers.