The IVF clinic of the future will combine a handful of technologies (the Gattaca stack):
1. In vitro gametogenesis (IvG) - make eggs from skin or blood cells (much less invasive)
2. Preimplantation genetic testing (PGT) - choose the embryo that best matches what you want, ideally from thousands or more (see #1)
3. Embryo editing - make further edits for disease prevention, or enhancement
4. Artificial Wombs - removes the risk/burden of pregnancy
Lots of work to get there, but this may help with the decline in birth rates. And it would start to accelerate evolution (which, by natural selection, is a very slow process, and only optimizes for survival and replication).
We banned human cloning shockingly fast. One year between Dollyโs birth and the US banning federal funding for human cloning. 1.5 years to countries banning it.
Tech is much more powerful now. If Dolly had been born today, I wonder if human cloning would get banned at all.
R3 Bio has a bold idea for replacing lab animals: genetically-engineered whole organ systems that lack a brain. The long-term goal, says a cofounder, is to make human versions. https://t.co/vjGSj4SUVF
Birth rates and headcounts are becoming as irrelevant as tracking horse populations in 1935 to predict transportation capacity. Reproduction is exiting the biology-constrained era and entering the capital and technology-mediated era.
Claude can now securely connect to your health data.
Four new integrations are now available in beta: Apple Health (iOS), Health Connect (Android), HealthEx, and Function Health.
The IVF process has completely automated the "sex" in sexual reproduction:
- sperm processing
- egg identification/preparation
- ICSI (intracytoplasmic sperm injection)
- incubation
- vitrification/thawing
Next is complete automation of ex utero embryo implantation and gestation (artificial wombs).
How do we go from a single cell to a complex organism?
For 50 yrs experimentally meeting the nutritional demands of a growing organism has been a bottleneck in development.
For the first time, we built placental support and predictive tools to make it possible.
Watch โ
How do we go from a single cell to a complex organism?
For 50 yrs experimentally meeting the nutritional demands of a growing organism has been a bottleneck in development.
For the first time, we built placental support and predictive tools to make it possible.
Watch โ