Estimating Clonal Dynamics Using Coalescent Theory and Branching Processes
Explore a 39-minute lecture on estimating clonal dynamics through coalescent theory and branching processes, delivered by Kit Curtius from the University of California, San Diego. Delve into the intersection of mathematics and oncology as part of the Fie…
Population Genomic Screening in Primary Care - Pre-Application Webinar
Attend a 59-minute webinar hosted by the National Human Genome Research Institute on September 10, 2024, focusing on the pre-application process for Population Genomic Screening in Primary Care Notices of Funding Opportunities (NOFOs). Learn about the im…
Evolutionary Rescue as a Framework for Understanding Drug Resistance in Cancer
Explore evolutionary rescue's role in cancer drug resistance, examining its impact on treatment strategies and tumor adaptation.
Genetic Composition of Supercritical Branching Populations Under Power Law Mutation Rate
Explore genetic composition in supercritical branching populations, focusing on power law mutation rates and their implications for evolutionary dynamics.
Carrier Screening Recommendations for Pregnant and Family Planning Individuals
Learn about carrier screening recommendations, test options, and family history considerations for pregnancy and family planning.
I Have a Family Member with Dementia - Am I at Risk?
Explore genetic factors in dementia, understand testing options, and learn about the rarity of hereditary causes in this informative presentation by a genetic counselor.
Spline-Switching Antisense Oligonucleotides for the Treatment of Disease
Explore cutting-edge spline-switching antisense oligonucleotides as a novel therapeutic approach for disease treatment. Gain insights into this innovative molecular technique and its potential medical applications.
NextGen Genomic Medicine - Making Variants of Unknown Significance Obsolete
Explore cutting-edge genomic medicine and its impact on understanding genetic variants. Learn how advanced techniques are revolutionizing the interpretation of previously unknown genetic variations in cardiovascular health.
Genetic Testing for SCD-Predisposing Cardiomyopathies and Channelopathies
Explore genetic testing for sudden cardiac death-predisposing heart conditions, focusing on yield, impact, and interpretation for personalized medicine in cardiomyopathies and channelopathies.
From Functional Genomics to Applied Physiology: Etiology and Treatment of Congenital Heart Disease
Explore functional genomics and applied physiology in congenital heart disease, covering etiology and treatment approaches. Gain insights into cardiovascular research and clinical applications.
MPG Primer: Introduction to Fine-Mapping - 2023
Explore fine-mapping techniques in genetics, covering basic principles, statistical methods, and applications in identifying causal variants for complex traits and diseases.
New Perspectives on Diabetes: The Many Subtypes of Type 2
Explore genetic insights into type 2 diabetes subtypes, their implications for patient care, and future research directions in this comprehensive discussion.
Beyond Cells: The Importance of Gene Programs and Tissue Context
Explore gene programs and tissue context beyond individual cells, uncovering novel insights into pressing biomedical questions through advanced machine learning techniques.
Polygenic Prediction Across Populations - Ancestry, Genetic Architecture, and Methodological Considerations
Explore polygenic prediction across populations, examining ancestry, genetic architecture, and methodological considerations for improved understanding of complex trait genetics.
Medical and Population Genetics Primer: All of Us Research Program - Part 2
Explore advanced concepts in medical and population genetics, focusing on complex trait analysis, human genetic variation, and cutting-edge sequencing methods.
Advancing the Toolchain for Interpreting Human Genetic Variation Using Deep Learning and Single-Cell Genomics
Explore deep learning and single-cell genomics tools for interpreting human genetic variation with Oliver Stegle from EMBL and DKFZ.
A Practical Guide to Bulk RNA-seq, Including Guidelines for eQTL Analysis - 2024
Explore practical bulk RNA-seq techniques and eQTL analysis guidelines in this comprehensive guide for medical and population genetics researchers.
Patient Engagement in Genomic Research: Using Social Media to Create a Community - 2024
Explore patient engagement in genomic research through social media, building communities for enhanced collaboration and participation.
Climbing Ladders to Cures in Rare Disease Research - Rare Disease Day 2024
Explore cutting-edge research and innovative approaches in rare disease treatment, from interventional genetics to biotech development, with insights from leading experts in the field.
Structural Variation in Human Genomes - MPG Primer 2024
Explore structural variations in human genomes, their impact on genetics, and cutting-edge analysis techniques with experts from the Broad Institute.
MPG Primer: Ethical Considerations in Genomics Research - 2024
Explore ethical considerations in genomics research, covering key principles and challenges in this rapidly evolving field. Gain insights into responsible practices and decision-making.