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I see.
Right. Why doesn't other steppe group work well? I will try but Saami and Udmurt, Mari are still roughly around 10% EEF as you estimated earlier?Originally Posted by Token
Would that be Finns and other Uralics like Saami, Udmurt, Mari or some group like Chuvash?Originally Posted by Token
That's strange. But I think it make sense as people of West Eurasian origin are much more interested in genetics than East Eurasians. In fact, most people of East Asian/any other ENA origin I know, barely know anything about genetics outside of 23andme and gedmatch calculators. Have you seen an African PCA based on qpAdm?Originally Posted by Token
That's ok. Im wondering though that if a Global PCA based on qpAdm results is created, would it still be affected by drift or any other factors?
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Archeogenetics is still trying to figure that out.
Yes.
No because these have substantial East Eurasian admixture.
No.
qpAdm is much less affected by recent population-specific drift.
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Sadly I've come to realize this too.That would be a complete waste of time considering that the vast majority can't even use Global25 properly.
No not affected by drift since qpAdm uses outgroups to mitigate but you still would have to look at other PCs besides PC1 and PC2Im wondering though that if a Global PCA based on qpAdm results is created, would it still be affected by drift or any other factors?
So both AG3 and MA1 are HAPLOID genomes meaning that they're not accurate because any actual hetrozygous positions have been genotyped as homozygous. So they're about 30%+ wrong. To make things worse, MA1 has 1x coverage and AG3 something like 0.2x coverage if I remember. People here should familiarize themselves with the concept of coverage if they want to get serious about leaning some basics
It would be immensely more accurate to use DIPLOID genomes such as the 30kya Yana Ancient Siberian which has 25x coverage or the 10Kya Ancient PaleoSiberian Kolyma genome with 14x coverage !! Other DIPLOID ancients that are available are Yamnaya Karagash and Botai and Ust Ishim and Stuttgart and Loschbour.
When talking about genetic similarity you'll get wildly different results depending on the tool used. But more basic than than are you asking maximum IBS similarity or actual IBD decent ?
Luckily ANE is old enough so the confounding factor that occurs with more recent BA genomes is not there. Meaning having to worry about whether the SNP between ANE and test subject is the same due to common ancient origin vs direct decent. Being as old as they are also means that every Eurasian is descended from them to some degree. I think Mansi and Nenets should be up there.
Lastly, you'll get very different results whether you use WGS vs limited number of SNPs from commercial genotyping companies such as 23andMe
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I see.
Thanks for confirming it. I will still try to break the components for fun.Originally Posted by Token
Would it be Scandinavians like Norwegians, Swedes, etc then?Originally Posted by Token
Alright. Would be nice to see one though.Originally Posted by Token
I see. Would be nice if Davidski can create a Global PCA based on qpAdm.Originally Posted by Token
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If you try to utilize Uralics as the closest modern day proxy for West Eurasian ancestry in Amerindians, the fit will be very bad since Uralics have some WHG and Basal Eurasian which Amerindians lack.
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Maguzanci, why are you so insistent in NOT simply using ANE to model Amerindians, when people keep telling you that nothing else will work?
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