Paul Bromann
Two Industry Leaders on the Growing Complexity of Genomic Cancer Data
How Do You Train Genomics AI? On Natural Selection Itself, Says VP of Illumina's AI Lab, Kyle Farh
Illumina Scales Variant Calling and Genome Interpretation to Improve Gaps in Genetic Testing
ctDNA-guided treatment in colorectal cancer
Does finding a rare mutation accomplish anything?
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: Clinical Metagenomics
Metagenomics in the Time of Covid-19: Emerging Pathogens
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
Whole Genome Sequencing Improves Diagnostic Yield
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
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