Applying Somatic Germline Testing for Lynch Syndrome
Explore paired tumor/germline testing for Lynch syndrome, its benefits, and comparison to other strategies. Learn to navigate discordant results and understand current literature on somatic genetic testing.
Ambry's Translational Genomics Lab: Understanding Variants of Uncertain Significance
Overview of Ambry's Translational Genomics Lab services for assessing variants of uncertain significance, focusing on RNA protocol for splicing variants to improve diagnostic yield and guide patient treatment.
Exome Testing - An Evidence-Based Approach to Accurate Diagnosis
Explore Ambry's evidence-based approach to clinical exome sequencing, including their proprietary scoring system for linking genes to diseases, leading to higher diagnostic yields and improved patient care.
Cardiovascular Genetic Testing Practices Around the World - Inherited Arrhythmias Series, Part 3
Explore global approaches to cardiovascular genetic testing for inherited arrhythmias, comparing diagnostic processes in Canada, Europe, and the US with insights from experts.
The Pregnancy Journey with Inherited Arrhythmia - Inherited Arrhythmias Series, Part 1
Comprehensive exploration of medical, physiological, and emotional aspects of maternal and fetal care during pregnancies affected by Long QT syndrome, featuring insights from doctors, genetic counselors, and patient experiences.
Genetic Testing for Neurodevelopmental Disorders
Explore genetic testing methods for neurodevelopmental disorders, including microarray, single syndrome, multi-gene panels, and diagnostic exome sequencing, to aid in diagnosing conditions like autism and epilepsy.
Clinical Diagnostic Exome Sequencing - Addressing Clinical Utility and Cost-Effectiveness
Explore clinical diagnostic exome sequencing's utility and cost-effectiveness with experts discussing its role in the diagnostic process and impact on patient care.
Genetic Testing in Hereditary Hemorrhagic Telangiectasia
Explore genetic testing for Hereditary Hemorrhagic Telangiectasia with expert Katie Wusik. Learn about clinical diagnosis, recent research, and the impact on patients and families.
Clinical and Management Implications of Exome Sequencing
Explore the clinical and management implications of diagnostic exome sequencing, examining current scientific evidence and its impact on genetic testing practices.
Genetic Testing for Young High-Risk Women
Empowering young high-risk women through genetic testing, featuring insights on inherited gene mutations and personal experiences from Bright Pink members.
Utilizing Exome Sequencing in Pediatric and Neonatal Clinical Settings
Explore the clinical applications of diagnostic exome sequencing in pediatric and neonatal settings, focusing on Ambry's ExomeNext and ExomeNext-Rapid tools for improved patient care.
At-Home Genetic Testing: Helpful or Harmful?
Explore the implications of at-home genetic testing kits with experts, discussing their accuracy, benefits, and potential risks in this informative public discussion event.
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.
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.
Simplifying Somatic NGS Analysis and Reducing Literature Review Time with HSMD
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.
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.
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.
What If - Everyone Had Their Genome Sequenced at Birth
Experts discuss the implications of universal genome sequencing at birth, exploring potential benefits, ethical concerns, and societal impacts of personalized genetic health data.
What Your Ancestors Can Tell You About Cancer Risk
Discover how family history impacts cancer risk and learn personalized strategies to reduce it. Explore genetic counseling's role in empowering proactive healthcare decisions and beating cancer.
Mastering the Mic: Interview Strategies for Science Communicators
Discover interview strategies for science communication with podcast host Kira Dineen. Learn podcast basics, networking tips, and effective interviewing techniques to enhance your skills as a host or guest.