Very relieved that it eventually had the intended result. Shocking amounts of time and resources are still being wasted on candidate gene results.
Very relieved that it eventually had the intended result. Shocking amounts of time and resources are still being wasted on candidate gene results.
www.lesswrong.com/posts/DfrSZa...
www.lesswrong.com/posts/DfrSZa...
And it will probably continue to get naively cited by authors outside ancient DNA, many of whom will never learn about the rebuttal: 2/2
And it will probably continue to get naively cited by authors outside ancient DNA, many of whom will never learn about the rebuttal: 2/2
The EA Forum has a whole section on "criticism of effective altruism" with many well-read and up-voted posts.
The EA Forum has a whole section on "criticism of effective altruism" with many well-read and up-voted posts.
Huge interest in short-sleep etc variants (candidate gene nonsense), embryo selection for cognitive traits (extremely low real-life predictive ability), and Jiankui He (charlatan whose human gene editing totally failed AND made many off-target edits)
Huge interest in short-sleep etc variants (candidate gene nonsense), embryo selection for cognitive traits (extremely low real-life predictive ability), and Jiankui He (charlatan whose human gene editing totally failed AND made many off-target edits)
Was quiet for a while but there's now a lot of activity and discussion – probably more than what remains on here. Recommend making the jump if you haven't already!
Image via @salonium includes some tools to help you start:
Was quiet for a while but there's now a lot of activity and discussion – probably more than what remains on here. Recommend making the jump if you haven't already!
Image via @salonium includes some tools to help you start:
A notable addition is a fork of the ISOGG 2019 tree in which we correct the placement of 4k mutations by analysing 300k Y chromosomes.
Repo in reply - see my thread on "the other place" for details:
A notable addition is a fork of the ISOGG 2019 tree in which we correct the placement of 4k mutations by analysing 300k Y chromosomes.
Repo in reply - see my thread on "the other place" for details:
After amending the DYS389i issue, Icelandic haplotypes become integrated with the rest of the network. 3/4
After amending the DYS389i issue, Icelandic haplotypes become integrated with the rest of the network. 3/4
The repeat counts for the DYS389i STR (and thus DYS389ii) seem deflated by 3 for Icelandic samples. 1/4
The repeat counts for the DYS389i STR (and thus DYS389ii) seem deflated by 3 for Icelandic samples. 1/4