Genomic Medicine XV: Laying the Groundwork for Population Genomic Screening - Session 1
Explore genomic medicine's current state, barriers, and future in population screening. Experts discuss technologies, clinical impact, and research directions for expanded genomic screening in the U.S.
DNA Science and Human Genetics - Journeys in Human Genetics and Genomics Colloquium
Explore DNA science and human genetics with Dr. Lawrence Brody, covering scientific, clinical, and societal aspects of genomics and potential career opportunities in the field.
The Role of Genetic Diagnosis in Inherited Cardiac Conditions - Part 1
Explore genetic diagnosis in inherited cardiac conditions, focusing on its importance, challenges, and advancements in cardiovascular genomic medicine.
The Role of Genetics in Modern Obstetrics - Saving Lives Through Prenatal Testing
Explore genetic testing's potential to identify disorders early, change lives, and build a healthier future. Learn about chromosomal disorders, screening methods, and the impact of fetal medicine.
Evaluating the Potential Benefits of Embryo Screening Using Polygenic Scores for Multiple Traits
Explore the potential and limitations of embryo screening using polygenic scores for multiple traits. Analyze ethical considerations and scientific challenges in this emerging field of reproductive genetics.
Implementing CGP and HRD Testing In-House for Advanced Cancer Care
Explore implementing CGP and HRD testing in healthcare, covering technical aspects, concordance with other assays, and benefits of in-house testing for matching patients with therapies.
Recommendations for Interpretation of Low Penetrance Variants and Risk Alleles
Explore challenges and recommendations for interpreting low penetrance variants and risk alleles in cancer genomics, improving harmonization across molecular diagnostics.
Real World Classification of Variants in Cancer Using ClinGen/CGC/VICC Oncogenicity Recommendations
Explore standardized classification of oncogenic somatic variants in cancer, improving consistency through validated SOP and real-world case demonstrations.
Advancing Medicine Through Global Collaboration
Explore global efforts in clinical genomics, from diagnosis to gene discovery. Learn about overcoming barriers and building infrastructure for integrating genomics into medical practice.
Application of Next Generation Sequencing Technologies in In Vitro Fertilization
Explore NGS technologies' application in IVF, enhancing genetic screening and embryo selection for improved fertility outcomes.
Internalizing a Comprehensive Genomic Profiling Solution with a Path to Reimbursement
Explore comprehensive genomic profiling solutions for cancer diagnosis, focusing on internalizing processes, overcoming challenges, and securing reimbursement pathways.
Investigation of Pathogenic and Truncated Variants of RUNX1 and DDX41 in All of Us
Explore pathogenic and truncated variants of RUNX1 and DDX41 genes in the All of Us research program, focusing on their implications for cancer genomics and personalized medicine.
Chromosomal Microarray Analysis for Hypocellular MDS Patients with Inconclusive Cytogenetics
Explore chromosomal microarray analysis for hypocellular MDS patients with inconclusive cytogenetics, enhancing diagnostic accuracy and treatment decisions in cancer genomics.
Reduced Performance of Centromere 15 Probe in Association with African Ancestry
Explore the impact of African ancestry on centromere 15 probe performance in cancer genomics, enhancing diagnostic accuracy for diverse patient populations.
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.
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.
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.
The Problem With Race-Based Medicine - TED
Exposing myths of race-based medicine, exploring genetic testing, social constructs, and evidence-based approaches to challenge harmful medical practices and assumptions.