All Episodes
Behind the Genes — 102 episodes
What does a midwife do?
How is genomic research being guided by patient and participant voices?
What is the Participant Panel at Genomics England?
What if a treatment created for one person could transform care for thousands?
What is de-identified data?
Can blood cancer be inherited?
What is informed consent?
What Does the Diagnostic Odyssey Really Mean for Families?
Reflecting on 2025 - Collaborating for the future of genomic healthcare
How can genomics help us understand cancer?
What is a genetic counsellor?
What is the Genomics England Research Environment?
How are families and hospitals bringing the Generation Study to life?
What is a clinical geneticist?
How can cross-sector collaborations drive responsible use of AI for genomic innovation?
How do people feel about using genomic data to guide health across a lifetime?
How can we enable ethical and inclusive research to thrive?
What can we learn from the Generation Study?
Can patient collaboration shape the future of therapies for rare conditions?
Can genomic research close the diagnostic gap in inherited sight loss?
How can we unlock the potential of large-scale health datasets?
What is the diagnostic odyssey?
How can parental insights transform care for rare genetic conditions?
Reflecting on 2024 - A year of change and discovery
What happens when I go for whole genome sequencing?
How can we work with patients to drive research initiatives?
Are genetic conditions always inherited from parents?
Can genetic discoveries revolutionise bowel cancer care?
What does 'no primary findings' mean?
What do parents want to know about the Generation Study?
What happens in a clinical trial?
How does X-linked inheritance work?
What is a polygenic disorder?
How has design research shaped the Generation Study?
Which healthcare professionals are involved in my genomic healthcare journey?
How can we ensure equitable access to genomic medicine?
How can organisations support those living with sickle cell?
How can we bridge the gap between diverse communities?
Can genomic testing prevent adverse drug reactions?
How has a groundbreaking genomic discovery impacted thousands worldwide?
How can we work in partnership towards a new era of genomic medicine and research?
How do pharmaceutical companies use genomic data for drug discovery?
Why do we need to consider ethics in genomic healthcare and research?
What is personalised medicine?
What is 'ethics'?
Why is diversity important in genomics research?
What is genetic or genomic testing?
Shining a light on rare conditions
What is the difference between DNA and RNA?
Hope for those with "no primary findings"
What is a variant of uncertain significance?
Treating Mila - Lessons for those living with rare conditions
What is the Generation Study?
Celebrating genomic breakthroughs - Insights from the Festival of Genomics
What is a rare condition?
Can Artificial Intelligence accelerate the impact of genomics?
Providing tailored care for cancer patients through whole genome sequencing
Reflecting on 2023 - A year of podcasts and a decade of progress
How are genetic tests transforming cancer prevention?
Transforming the NHS with genomic testing
How can Genetic Counsellors improve care through research?
Why is diversity in Parkinson’s research so important?
Which conditions will we look for initially in the Generation Study?
Can genomics improve our understanding of childhood cancers?
Early Career Researchers navigating the field of genomics
How can we overcome bias in healthtech?
What is a bioinformatician?
Genomic newborn screening for rare diseases – a review
What is multimodal data?
The journey to the Human Genome Project and beyond with Dr Francis Collins
What is long-read vs short-read sequencing?
How can advances in genome sequencing support patients through their sarcoma journey?
What is the National Genomic Research Library?
Reaching the full potential of genomic research
Research priorities for sickle cell and genomics
What is whole genome sequencing?
How can we support complex patient journeys?
The impact of a genetic diagnosis on mental health
What is a genome?
Our Nurses, Our Future
What are the challenges of data governance in the digital age?
Genetics vs genomics, what’s the difference?
Public views on genetics - what have we learnt?
Prostate cancer awareness with The Errol McKellar Foundation and friends of Caswell Thompson
Why data isn’t neutral
The Participant Panel - What are you doing to keep my data safe?
Chris Wigley: Goodbye 2022, hello 2023!
Making research relevant to the user
The last 10 years and the next...
Conversations with the CEOs of genomics
What does it take to scale an idea like whole genome sequencing diagnostics across an entire health service?
What role do genetic counsellors play in healthcare?
The importance of patients being at the heart of the research.
The song of the cell
Health equity engagement of special populations
The Muslim Census - attitudes towards health research and genomics
Not quantity of life, quality of life - my journey with breast cancer
The Sherlock Holmes moment
A conversation with the CEO of the Danish National Genome Centre
Mila’s story - from Mila to millions
Philanthropy and venture funding the future of cancer care
The patient’s voice