
Illumina Genomics Podcast
Hear directly from the people whose work in genomics is shaping the way we think about science and our world. Listen as leading scientists discuss the impact of genomics with the Illumina Scientific Affairs team. Download or subscribe to our recurring podcasts.
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
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