Illumina Genomics Podcast
By Illumina, Inc.
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Category: Life Sciences
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Subscribers: 41
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Episodes: 158
Description
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.
| Episode | Date |
|---|---|
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Two Industry Leaders on the Growing Complexity of Genomic Cancer Data
|
Apr 18, 2024 |
|
How Do You Train Genomics AI? On Natural Selection Itself, Says VP of Illumina's AI Lab, Kyle Farh
|
Apr 18, 2024 |
|
Illumina Scales Variant Calling and Genome Interpretation to Improve Gaps in Genetic Testing
|
Apr 18, 2024 |
|
Clinical utility of ctDNA testing in lung cancer
|
Apr 10, 2024 |
|
ctDNA-guided treatment in colorectal cancer
|
Apr 10, 2024 |
|
Does finding a rare mutation accomplish anything?
|
Apr 10, 2024 |
|
Liquid biopsy NGS in cancer care
|
Apr 26, 2023 |
|
Genetic counselling in an era of prenatal screening, tools to support patient informed consent
|
Apr 03, 2023 |
|
Homologous Recombination Deficiency (HRD) Testing in Ovarian Cancer
|
Nov 11, 2022 |
|
Testing for NTRK Fusions
|
Nov 11, 2022 |
|
Pharmacogenomics: Barriers and Opportunities to Implementation
|
Apr 26, 2021 |
|
The Impact of Pharmacogenomics on Precision Medicine
|
Apr 21, 2021 |
|
Metagenomics in the Time of Covid-19: Clinical Metagenomics
|
Apr 01, 2021 |
|
Metagenomics in the Time of Covid-19: Emerging Pathogens
|
Apr 01, 2021 |
|
Genomic Surveillance and Testing for SARS-CoV-2
|
Mar 16, 2021 |
|
Exploring the Genomic Diversity of Africa
|
Mar 01, 2021 |
|
Developmental Biology Meets Immunotherapy
|
Sep 03, 2020 |
|
Genomics and the End of the Diagnostic Odyssey
|
May 13, 2020 |
|
Standardization of Clinical Whole Genome Sequencing
|
May 11, 2020 |
|
Rapid Genome Sequencing of Critically Ill Children
|
Apr 29, 2020 |
|
Integrating Genomics with Behavioral Sciences
|
Apr 22, 2020 |
|
Growing the Invertebrate Tree of Life with Genomics
|
Apr 01, 2020 |
|
DNA Structural Variants from Microscope to Sequencer
|
Mar 19, 2020 |
|
Finding Rare Diseases and Genome Sequencing
|
Mar 04, 2020 |
|
Genomics of Diet and Precision Nutrition
|
Feb 19, 2020 |
|
Drug Discovery through Gene Regulation
|
Feb 06, 2020 |
|
2019 and the Year in Genomics
|
Jan 22, 2020 |
|
Comprehensive Genomic Tumor Profiling
|
Dec 11, 2019 |
|
Genomic Tumor Profiling and Precision Oncology
|
Nov 20, 2019 |
|
Genomics and Feeding a Hungry World
|
Nov 06, 2019 |
|
If Tumors Could Talk
|
Oct 23, 2019 |
|
NGS and New Frontiers in Infectious Disease
|
Oct 09, 2019 |
|
DNA Stories of Australia’s First Peoples
|
Sep 25, 2019 |
|
NGS Improves In Vitro Fertilization
|
Sep 11, 2019 |
|
Genetic Screening and Inherited Disorders
|
Aug 29, 2019 |
|
Sequencing the Cancer Epigenome
|
Aug 14, 2019 |
|
Genomics and Tiger Conservation in Nepal
|
Jul 31, 2019 |
|
Escape from Limbo Land
|
Jul 17, 2019 |
|
Unravelling the Mystery of Autoimmunity
|
Jul 08, 2019 |
|
Single Cell Omics and Cellular Immunology
|
Jun 19, 2019 |
|
Neglected Diseases and the Impact of NGS
|
Jun 05, 2019 |
|
Rare Disease and the Diagnostic Odyssey
|
May 23, 2019 |
|
Finding Bad Bugs with NGS
|
May 08, 2019 |
|
Genetics of Breast Cancer
|
Apr 25, 2019 |
|
Next Generation Science Education
|
Apr 08, 2019 |
|
Ancient DNA and Human History
|
Mar 20, 2019 |
|
The Magic of Stem Cells and Embryogenesis
|
Mar 06, 2019 |
|
Immune Cells and Their Search for Energy
|
Feb 21, 2019 |
|
Environmental and Societal Impact of Microbes
|
Feb 06, 2019 |
|
Genomics 2018 Looking Back and Looking Ahead
|
Jan 23, 2019 |
|
Estonia is a Model for Precision Healthcare
|
Jan 09, 2019 |
|
RNA Sequencing is a Cell Biology Tool
|
Dec 18, 2018 |
|
Genome Editing and CRISPR-Cas9
|
Dec 11, 2018 |
|
Noninvasive Prenatal Testing and NIPT
|
Nov 01, 2018 |
|
Genomics of Long-Term Memory
|
Oct 18, 2018 |
|
Genome Assembly and A Genomic Jigsaw Puzzle
|
Oct 03, 2018 |
|
Genetics of Deafness and Hearing Loss
|
Sep 19, 2018 |
|
Genetics of Autism and Psychiatric Disorders
|
Sep 05, 2018 |
|
Genomics and Preimplantation Genetic Screening
|
Aug 23, 2018 |
|
Large Scale Genetic Risk Profiling in Dementia
|
Aug 09, 2018 |
|
Eczema and the Human Skin Microbiome
|
Jul 12, 2018 |
|
Using Genetics to Predict Heart Attack Risk
|
Jun 27, 2018 |
|
Out of Africa and Genetics of the African Diaspora
|
Jun 15, 2018 |
|
Cancer Epigenomics and A Cacophony of Gene Expression
|
Jun 07, 2018 |
|
Rare Genes and Rare Diseases
|
May 23, 2018 |
|
NHGRI's 2020 Vision for Genomics
|
Apr 22, 2018 |
|
Genetics of Children's Complex Diseases From GWAS to NGS
|
Apr 11, 2018 |
|
Genomics of Endosymbiosis and Cells Within Cells
|
Mar 29, 2018 |
|
Brain on Fire and Genomics of Neuroinflammation
|
Mar 14, 2018 |
|
Human Gut Microbiome and Beneficial Bacteria
|
Feb 22, 2018 |
|
Single Cell Genomics and Cell Ontology
|
Feb 08, 2018 |
|
The Human Genome and What We Are Missing
|
Jan 25, 2018 |
|
Human Microbiome and Our Second Human Genome
|
Nov 27, 2017 |
|
Targeted NGS Empowers Genetic Testing
|
Nov 03, 2017 |
|
Childhood Cancer Risk and Genetics
|
Oct 20, 2017 |
|
Genomics and Protecting Endangered Species
|
Oct 06, 2017 |
|
Making Sense of Cancer Genomes
|
Sep 22, 2017 |
|
RNA Sequencing in Diagnostics
|
Sep 08, 2017 |
|
Genomics and Immune Diseases
|
Aug 25, 2017 |
|
Food Spoilage and Genomics
|
Aug 10, 2017 |
|
Finnish Genetics Aid Disease Research
|
Jul 07, 2017 |
|
The EMBL Genomics Core Facility
|
Jun 06, 2017 |
|
Uncovering Enhancer Hijacking Events in Cancer
|
May 23, 2017 |
|
Single-Cell Genomics and Mars
|
Mar 30, 2017 |