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About Biomedical Basics
Biomedical Basics are AI-generated explanations prepared with access to the complete collection, human-reviewed prior to publication. Short and simple, covering biomedical and life sciences fundamentals.
Topics Covered
- Ethical issues in genetics
- Genetic testing & consent
- Data privacy & security
- Genetic discrimination
- Gene editing & prenatal ethics
- Ownership in genetic research
- Ongoing ethical reflection
Talk Citation
(2026, June 30). Ethical issues in human genetics [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved July 1, 2026, from https://doi.org/10.69645/WTWK5942.Export Citation (RIS)
Publication History
- Published on June 30, 2026
Financial Disclosures
A selection of talks on Genetics & Epigenetics
Transcript
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0:00
The topic of ethical issues
in human genetics will be
explored through the
ethical challenges
arising from advances
in human genetics,
including genetic
testing, data privacy,
and the risk of discrimination.
We will discuss dilemmas
relating to consent,
data ownership,
and the impact of
new technologies like gene
editing and prenatal testing.
Issues of justice, autonomy,
and benefit sharing in
research will be explored
alongside the ongoing
responsibility to
engage in ethical
reflection and dialogue.
Throughout, we will emphasize
the need to protect
both individual rights and
the wider interests of society.
Rapid advances in
genetic science have
revolutionized our understanding
of health and disease,
while bringing complex ethical
challenges from the power of
genetic testing and
personalized medicine
to concerns about privacy,
discrimination and gene editing,
our use of genetics must be
guided by ethical reflection.
Society now faces profound
dilemmas surrounding autonomy,
justice, and the very definition
of what it means to be human.
Genetic testing, whether
for disease risk,
diagnosis or guiding therapy,
offers invaluable insights, but
also introduces significant
ethical challenges.
Informed consent
is a major concern
as genetic results
can impact families,
making truly informed
consent complex.
Tests may reveal far
reaching information
such as unexpected disease
risk or paternity.
Privacy is central involving
questions about who controls
this sensitive data and
the effectiveness of
existing protections.