Flash Forward is a show about possible (and not so possible) future scenarios. What would the warranty on a sex robot look like? How would diplomacy work if we couldn’t lie? Could there ever be a fecal transplant black market? (Complicated, it wouldn’t, and yes, respectively, in case you’re curious.) Hosted and produced by award winning science journalist Rose Eveleth, each episode combines audio drama and journalism to go deep on potential tomorrows, and uncovers what those futures might re ...
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S4E06: It's Personal: Inclusive Research and Precision Medicine
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Manage episode 334816164 series 2983987
Content provided by Two Scientists Walk Into a Bar. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Two Scientists Walk Into a Bar or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
Achieving the first complete sequence of a human genome via the Human Genome Project represents an incredible feat – but it’s just the tip of the iceberg when it comes to unlocking the power of genomics for drug discovery and development. As the scientific community builds on our understanding of genomics, one of the most critical questions becomes, how can we thoughtfully collect and use genetic data to better understand and support the health of all communities, including those who are underrepresented in clinical research. Co-host Maria Wilson sits down with Mark McCarthy, Principal Fellow and Executive Director of Human Genetics, to explore the interplay between genetics, research, and health impact and the potential for more diverse genetic data to reflect the populations of people who experience the diseases we are studying and expand access to quality healthcare for all. This episode is the first in a two-part series dedicated to inclusivity in research. Read the full text transcript at: www.gene.com/stories/its-personal-inclusive-research-and-precision-medicine
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46 episodes
MP3•Episode home
Manage episode 334816164 series 2983987
Content provided by Two Scientists Walk Into a Bar. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Two Scientists Walk Into a Bar or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
Achieving the first complete sequence of a human genome via the Human Genome Project represents an incredible feat – but it’s just the tip of the iceberg when it comes to unlocking the power of genomics for drug discovery and development. As the scientific community builds on our understanding of genomics, one of the most critical questions becomes, how can we thoughtfully collect and use genetic data to better understand and support the health of all communities, including those who are underrepresented in clinical research. Co-host Maria Wilson sits down with Mark McCarthy, Principal Fellow and Executive Director of Human Genetics, to explore the interplay between genetics, research, and health impact and the potential for more diverse genetic data to reflect the populations of people who experience the diseases we are studying and expand access to quality healthcare for all. This episode is the first in a two-part series dedicated to inclusivity in research. Read the full text transcript at: www.gene.com/stories/its-personal-inclusive-research-and-precision-medicine
…
continue reading
46 episodes
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