migtig
aka Mrs. Giant
I really have mixed feelings about this. Just because science makes it possible, should we do this? Part of me says yes, if I want a blue eyed dark haired little boy who would have no defects and perfect health, and I can afford this, then why shouldn't I have the perfect baby? Another part of me shudders and wonders what we will be breeding out of future generations. I think of 1984 and Brave New World and I'm frightened for our future.
Josef Mengele would say yes, we should create a perfect baby. After all, his research lead the way to make this possible.
IVF baby born using revolutionary genetic-screening process | Science | guardian.co.uk
Excerpt:
The first IVF baby to be screened using a procedure that can read every letter of the human genome has been born in the US.
Connor Levy was born on 18 May after a Philadelphia couple had cells from their IVF embryos sent to specialists in Oxford, who checked them for genetic abnormalities. The process helped doctors at the couple's fertility clinic in the US select embryos with the right number of chromosomes. These have a much higher chance of leading to a healthy baby.
The birth demonstrates how next-generation sequencing (NGS), which was developed to read whole genomes quickly and cheaply, is poised to transform the selection of embryos in IVF clinics. Though scientists only looked at chromosomes – the structures that hold genes – on this occasion, the falling cost of whole genome sequencing means doctors could soon read all the DNA of IVF embryos before choosing which to implant in the mother.
Josef Mengele would say yes, we should create a perfect baby. After all, his research lead the way to make this possible.
IVF baby born using revolutionary genetic-screening process | Science | guardian.co.uk
Excerpt:
The first IVF baby to be screened using a procedure that can read every letter of the human genome has been born in the US.
Connor Levy was born on 18 May after a Philadelphia couple had cells from their IVF embryos sent to specialists in Oxford, who checked them for genetic abnormalities. The process helped doctors at the couple's fertility clinic in the US select embryos with the right number of chromosomes. These have a much higher chance of leading to a healthy baby.
The birth demonstrates how next-generation sequencing (NGS), which was developed to read whole genomes quickly and cheaply, is poised to transform the selection of embryos in IVF clinics. Though scientists only looked at chromosomes – the structures that hold genes – on this occasion, the falling cost of whole genome sequencing means doctors could soon read all the DNA of IVF embryos before choosing which to implant in the mother.
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