All Episodes

AI Powered Multiomics: Joachim Schmid on Data Analysis at Illumina

The Genomic Revolution Transforming Public Health in Africa with Next-Generation Sequencing (NGS) with Professor Martin Nyaga

Illumina Scales Variant Calling and Genome Interpretation to Improve Gaps in Genetic Testing

How Do You Train Genomics AI? On Natural Selection Itself, Says VP of Illumina's AI Lab, Kyle Farh

Two Industry Leaders on the Growing Complexity of Genomic Cancer Data

Does finding a rare mutation accomplish anything?

ctDNA-guided treatment in colorectal cancer

Clinical utility of ctDNA testing in lung cancer

Liquid biopsy NGS in cancer care

Genetic counselling in an era of prenatal screening, tools to support patient informed consent

Testing for NTRK Fusions

Homologous Recombination Deficiency (HRD) Testing in Ovarian Cancer

Pharmacogenomics: Barriers and Opportunities to Implementation

The Impact of Pharmacogenomics on Precision Medicine

Metagenomics in the Time of Covid-19: Emerging Pathogens

Metagenomics in the Time of Covid-19: Clinical Metagenomics

Genomic Surveillance and Testing for SARS-CoV-2

Exploring the Genomic Diversity of Africa

Developmental Biology Meets Immunotherapy

Genomics and the End of the Diagnostic Odyssey

Standardization of Clinical Whole Genome Sequencing

Rapid Genome Sequencing of Critically Ill Children

Integrating Genomics with Behavioral Sciences

Growing the Invertebrate Tree of Life with Genomics

DNA Structural Variants from Microscope to Sequencer

Finding Rare Diseases and Genome Sequencing

Genomics of Diet and Precision Nutrition

Drug Discovery through Gene Regulation

2019 and the Year in Genomics

Comprehensive Genomic Tumor Profiling

Genomic Tumor Profiling and Precision Oncology

Genomics and Feeding a Hungry World

If Tumors Could Talk

NGS and New Frontiers in Infectious Disease

DNA Stories of Australia’s First Peoples

NGS Improves In Vitro Fertilization

Genetic Screening and Inherited Disorders

Sequencing the Cancer Epigenome

Genomics and Tiger Conservation in Nepal

Escape from Limbo Land

Unravelling the Mystery of Autoimmunity

Single Cell Omics and Cellular Immunology

Neglected Diseases and the Impact of NGS

Rare Disease and the Diagnostic Odyssey

Finding Bad Bugs with NGS

Genetics of Breast Cancer

Next Generation Science Education

Ancient DNA and Human History

The Magic of Stem Cells and Embryogenesis

Immune Cells and Their Search for Energy

Environmental and Societal Impact of Microbes

Genomics 2018 Looking Back and Looking Ahead

Estonia is a Model for Precision Healthcare

RNA Sequencing is a Cell Biology Tool

Genome Editing and CRISPR-Cas9

Noninvasive Prenatal Testing and NIPT

Genomics of Long-Term Memory

Genome Assembly and A Genomic Jigsaw Puzzle

Genetics of Deafness and Hearing Loss

Genetics of Autism and Psychiatric Disorders

Genomics and Preimplantation Genetic Screening

Large Scale Genetic Risk Profiling in Dementia

Eczema and the Human Skin Microbiome

Using Genetics to Predict Heart Attack Risk

Out of Africa and Genetics of the African Diaspora

Cancer Epigenomics and A Cacophony of Gene Expression

Rare Genes and Rare Diseases

NHGRI's 2020 Vision for Genomics

Genetics of Children's Complex Diseases From GWAS to NGS

Genomics of Endosymbiosis and Cells Within Cells

Brain on Fire and Genomics of Neuroinflammation

Human Gut Microbiome and Beneficial Bacteria

Single Cell Genomics and Cell Ontology

The Human Genome and What We Are Missing

Human Microbiome and Our Second Human Genome

Targeted NGS Empowers Genetic Testing

Childhood Cancer Risk and Genetics

Genomics and Protecting Endangered Species

Making Sense of Cancer Genomes

RNA Sequencing in Diagnostics

Genomics and Immune Diseases

Food Spoilage and Genomics

Finnish Genetics Aid Disease Research

The EMBL Genomics Core Facility

Uncovering Enhancer Hijacking Events in Cancer

Single-Cell Genomics and Mars