Read my responses carefully.
What TMR4A shows is that you would need to invoke rates of recombination, mutation, gene conversion, far in excess of what we observe today in order to generate the required diversity in just a few thousand years. At current rates, ~500,000 years is required. Thatās the point. if you have all these densely packed heterozygous sites then you need a lot of fine-scale (intragenic) recombination you break them and and produce new alleles from the created heterozygosity. This isnāt what we observe in modern populations.
Start a new topic if you want to discuss that.
You did?
I donāt do YouTube, but Iād definitely love a copy of the book. I donāt care enough about this debate to dedicate some thorough review of it (Iām also a paleontologist so this is somewhat out of my comfort zone) . Everyone accepts evolution and everyone accepts common ancestry. On all sides. The disagreements are how much can known evolutionary processes can accomplish, is the common ancestry separate or universal and over what timescales. Thatās not enough of a disagreement for me to care that much. But Iād be more than willing to read your book If youād provide it.
I have explained everything very thoroughly in my āwalls of textā. You seem to be incapable of reading through them in order to engaged in honest discussion. I do see why experts such as Jeanson Sanford and Carter would never bother with these blogs. I am quickly seeing why they are a waste of time. Like I said, I am going to enjoy analyzing this on my channel. I am still awaiting excitedly for some kind of response to my refutations in regards to the critics (evograd, Dan, etcā¦) misrepresentations of Jeansonās Y chromosome papers.
Define āalleleā for us the ācorrectā way then. Be as specific and detailed as possible.
Unbelievable. I have at least 3 times alone in this thread. I am done here.
Good talk guys.
Much like the previous thread I engaged in, I am yet again very enlightened.
I think everyone is.
Exactly what my latest video addresses as well as my comments here in this thread. And yet Swamidass accuses me of not understanding. This is a dishonest tactic and turns me off from participating in these discussions. In all fairness, it seemed like you did indeed understand what I was saying. Scroll up and look for my definition of alleles and you will see that I have answered this thoroughly. Dan even responded to my definition of alleles quite thoroughly in his most recent video.
Is it dishonest when you accuse us of misunderstanding?
One of two or more versions of a particular DNA positionā
It was buried DEEP in a wall of text
You gave this definition (Frelloās definition that Jeanson approved of):
But then later said:
A particular DNA position = a single nucleotide, so you seem to be contradicting yourself. Thatās why Iām asking for clarification.
Make a thread about it here then, and I promise that I (and maybe even others) will respond. This forum is a far better place to have these kinds of discussions than the comments section of a YouTube video that no one else will ever read.
Itās simply not worth my time to write detailed responses if only you will read them, Iād prefer to do it much more publicly. You should want the same thing, so I suggest again - make a thread here about it.
I have to second this. Canāt make sense of his given definition.
As I said earlier, Iād be happy to start a discussion if he isnāt. This time I could probably be more helpful by sitting down and summarizing his video, so thereās something to bite. Anyone interested?
Iām going to be the one to point out that having this conversation with someone who lacks a basic understanding of the relevant concepts is going to be challenging and confusing for the other participants.
I agree. I think explaining the concepts that are correct, clearly to people, is better than a detailed back and forth. Right now there is a gap. We havenāt really explained a lot of this in away that makes sense to most people.
Especially when the one who lacks the basic understanding has already made a strong commitment to not understanding and to remaining scientifically unaware.
I think explaining the concept of how TMR4A interacts with created heterozygosity graphically would be helpful. A diagram showing Adam and Eve with some created heterozygosity, how genomes change over generations in their offspring, and how the algorithms used in TMR4A reconstruct this history would be very valuable.
I also wonder if it might be helpful to show TMR4A working on simulated data. You could simulate 2 genomes with created heterozygosity, have the population grow and genomes recombine for a given period of time, then show that your method is accurate. This is standard practice in developing new popgen tools, after all.
Yes we have some unpublished data on this. I wonder if @GutsickGibbon might want to do a video on it too .
Any idea when/where youāll publish on this?