EGI Notes

Sunday, November 19, 2017

More Genetic Structure and DifferInt Analysis

An important topic.

I have been looking a bit more at the DifferInt program (currently unable to find anything better), testing some model genotypes to better understand the relationship between different levels of integration with respect to the amount of differentiation.  One finding which is clear that it is when genetic differentiation – at the lowest genepool level - between groups is shallow is when the program is scalable at the level of the highest level of integration.

A test model was devised with two populations of eleven individuals each.  Six loci were considered.  Initially, the two populations were constructed to be genetically identical. Four individuals of the second population had alleles at one lock rearranged so that four heterozygotes were made into four homozygotes (two of each type), without changing the total number of each allele type for that locus in that population.  After this change, the genepool differentiation was 0.0303, but the multilocus genotype neglecting elementary genic differences (MGNEGD) was 0.3636 – a twelve-fold increase in differentiation.  In this simple model of shallow genetic difference, a discrete representation of genetic structure (MGNEGD) is seen to exhibit sharply increased (and quantitatively scalable) differentiation with even a small change in allele structuring in genetically similar (model) populations.

However, when differentiation at the genepool level is already fairly high, then MGNEGD rises to complete differentiation quickly, and the ability to evaluate genetic structure becomes non-scalable using this program.  It could be that the SNP database I utilized for my initial human study was enriched in SNPs that sharply differentiate between ethnies and so all levels of differentiation were high in the analysis; perhaps completely random SNPs would be better? On the other hand, we are most concerned about the distinctive genome (with respect to EGI).  

In a more realistic model of human genetic differentiation, two populations were set up, each consisting of ten individuals, each assayed over 100 loci.  90 of these loci were absolutely identical between the two populations and 10 loci differed between the populations with respect to the frequencies of alleles at the loci.  In some cases, it was 100%  of one allele pair compared to 100% of another; in other cases it was more subtle - for example one population having 20% AA, 60% AT, and 20% TT while the other population was 20% AA, 50% AT, and 30% TT for the same locus.  The genepool differentiation between the two populations was 0.0370; the MGNEGD was 1.000 - complete differentiation.  This again shows that with enough loci studied and differentiated populations, analysis of discrete sets of multilocus genotypes (see my definition of genetic structure below) will reach complete differentiation.  The implications for genetic interests should be obvious.

It might be a good idea to review my idea of genetic structure again here.

Genetic structure as per my definition can be viewed as a form of linkage disequilibrium of alleles over all the loci in the genome, or this distinctive genome, of at least whatever number of loci that were assayed.  Each specific permutation of multilocus genotypes is a discrete entity, so that one would expect, of course, district genetic structures between any set of individuals who are not identical twins; there would be differences in genetic structure within families, never mind within ethnies.

However – and this is the key point that separates my idea from the run-of-the mill evaluations of genetic structure - I envision genetic structure to be defined by specific ranges of multilocus genotypes.  Therefore, while there is going to be, naturally, individual variation of discrete multilocus genotypes within families, there will be a family-specific range of multilocus genotypes, a range within which all the individual genotypes, of that family will fall within.  Likewise, there will be ethny-specific ranges of multilocus genotypes, so that members of an ethny will exhibit genotypes that – while they differ on an individual level – will fall within a range, a set, of genotypes characteristic of that ethny.  

It then follows, that while multilocus genotypes will be differentiated from each other, the extent of that differentiation will differ.  Different families will exhibit different ranges, or sets, of possible multilocus genotypes, but families belonging to the same ethny will exhibit ranges that are more similar to each other than that of families of different ethnies (the same goes for individuals of course, across families or across ethnies).  Ethnies belonging to the same continental population group (i.e., intra-racial) will exhibit more similar ranges of possibilities of multilocus genotypes than that of inter-racial comparisons.  One could think of it also as frequency distributions of multilocus genotypes, of all the alleles possibilities at all the relevant loci considered together as a discrete entity, and one can compare how similar the frequency distributions are, with more overlap from those more similar.  

One would also expect a solid correlation, or association, between the differentiation as measured by an allele-by-allele genepool/beanbag approach, single locus genotypes, and multilocus genotypes. The relative extent of differences should correlate in at least a qualitative sense between these levels of “genetic integration.”  Hence, as previously noted at this blog, “complete differentiation” at the multilocus genotype level should differ in extent dependent upon how similar or different the genotypes are from each other.  One should in theory be able to quantitate this in a continuous fashion, rather than just having a binary yes/no undifferentiated/completely differentiated choice.

This is obviously an important topic.  If we are to make decisions based on genetic interests, don’t we need to have a better understanding about what those interests actually are, quantitatively speaking?

It’s true that we know enough right now to justify taking action in defense of genetic interests; even at the lowest levels of genetic integration, and even with estimates of child equivalents based on Fst, we already know that mass migration of alien peoples is genocide.

So, yes, I’m sympathetic to the argument that in general, qualitatively speaking, it is more important to actualize a defense of the interests we already know about than to fine-tune our understanding of these interests. But why not both?  Nothing stops us from both organizing on a political and metapolitical level while at the same time continuing to refine our understanding of this topic.  While most of my work now concerns the political and metapolitical implications of defending EGI and of actualizing a High Culture, surely there is also a place for a better understanding of EGI and for a better understanding of Spenglerian cycles and how to control them foe civilizational benefit.

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Saturday, November 18, 2017

Born Neandertal

Biological realities.

Read here.  Neandertals were born, not ”made.”  

Neandertal and modern human adults differ in skeletal features of the cranium and postcranium, and it is clear that many of the cranial differences—although not all of them—are already present at the time of birth. We know less, however, about the developmental origins of the postcranial differences. Here, we address this deficiency with morphometric analyses of the postcrania of the two most complete Neandertal neonates—Mezmaiskaya 1 (from Russia) and Le Moustier 2 (from France)—and a recent human sample. We find that neonatal Neandertals already appear to possess the wide body, long pubis, and robust long bones of adult Neandertals. Taken together, current evidence indicates that skeletal differences between Neandertals and modern humans are largely established by the time of birth.

That’s interesting.  More relevant to issues of interest to this blog is the following from the same paper:

Adult European Americans and African Americans differ, on average, in the shapes of their long bones, with European Americans having thicker shafts and larger articulations relative to shaft length.

But, but, but…aren’t racial differences all “skin deep” – just about color – and that other than such trivialities, we are all “exactly the same?”  You mean, there are actual anatomical differences between the races (never mind the genetic gulf)?

Race denial is a farce.  Real racial science is caught between the laughable lies of the Left and the HBD pseudoscience and crazed ethnic fetishism of the Right.  Fighting the former doesn’t mean we have to accept the latter.  Both are wrong (but, admittedly, the former is more dangerous).

And speaking of the Left, and getting back to the main article, did anyone truly believe that extreme Neandertal robustness was somehow the result of lifestyle?  Is anti-genetic leftism so entrenched in science that it goes to that extreme of ludicrousness?   Were the Neandertals constructing makeshift barbells out of boulders and tree trunks and engaging in Ice Age powerlifting routines?  Granted, yes, I understand (unlike Der Movement) that things need to be demonstrated empirically, and not just assumed.  But still, one cannot pretend that a demonstration that Neandertal robustness was an inborn trait is any sort of grand discovery.  Only leftists would be surprised by this finding.

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Friday, November 17, 2017

Meet Shah Jorjani

Madness.

Let's take a look at some "movement" stupidity from several weeks ago.  I've been busy with the DifferInt analyses over the past few weeks, but will get around to evaluating Der Movement' s more recent antics when I have the time.

We can start with the following.

Since Greg Johnson quoted excerpts from Jorjani to, I presume, take another swipe at Spencer, let’s take a closer look at some other points Jorjani has to make.  When you read this, please remember that Jorjani has been taken seriously by BOTH Johnson and Spencer; he’s spoken at Counter-Currents events, and he was high in the councils of the Alt Right corporation (never mind Arktos).


….Croatia is a part of Iranian civilization. During Tito’s rule, which imposed a Slavic identity on all of Yugoslavia, scholars were actually prosecuted, imprisoned, and even tortured for researching and writing about the Iranian origin of the Croatian people. Specifically, they are part of the Scythian branch of Iranians – cousins of the Persians who rode deep into Europe.

Yes sir, Croatians are actually Iranians with a dastardly fake Slavic identity.  No doubt – no doubt whatsoever! – population genetics studies will place Croatians right there with Iranians and distant from those alien Balkan Slavs!  And if such studies don’t yield that result, then, by golly, it’s the ghost of Tito imposing an anti-Promethean contamination, falsifying the genetics!


Steve Bannon was known to be a reader of Arktos books and Michael’s plan was to send me into the White House to cultivate a relationship with Bannon, and through him, to influence President Trump. My main reason for wanting to have such influence was to help determine Iran policy.

As the Iron Sheik used to say, “Iran number one!”

…the funding for a capital investment that would have established me as the majority shareholder of the Alt-Right Corporation…

Very, very, very carefully consider the ramifications of this delusional Persian supremacist intimately involved with the Alt Right, a “movement” ostensibly representing the interests of indigenous Europeans.


This is about the reorientation of the trajectory of geopolitics in the Middle East, the Caucasus, and Central Asia. It is about aborting a Renaissance of the Persian Empire…

And at the heart of this world historical mission is…Jorjani.

Except that we are not Germans. 

No, you’re not.


Through the Scythians (i.e. the Saxons) and the Alans, we lent the Germans and Goths our Faustian (i.e. Zoroastrian) genius and chivalric spirit but those northern Barbarians never understood the essence of our cosmopolitan humanism.

Err...isn’t “cosmopolitan humanism” the very thing all the grand “traditionalists” of the Alt Right allegedly oppose?  Cosmopolitan humanism?  What would Evola think? Savitri Devi?  Oh, the Kali Yuga of it all!  The men who can’t tell time!  The Age of Iron!  Oh Guenon, where are thou?

Al-Ahwaz and a Kurdish nation have nothing but Sunni fundamentalism and barbaric tribalism to offer the world, whereas our Persian civilizational heritage has not only held Iran together for centuries it has, repeatedly, offered all of humanity the best chance at forming a world order based on innovation, compassion, and social justice.

Social justice?  I guess that goes along with all of the “cosmopolitan humanism.”  How about multiculturalism?  The wonderfully cosmopolitan Persian Empire was multicultural, no?  Let’s have the Alt Right fight for multicultural cosmopolitan humanist social justice!  

We know that you do not really have a government “of the people, by the people, and for the people.” You are oppressed by a rogue dictatorship. Rest assured that after we liberate ourselves and secure our future, we will bring the ever-living fire of true freedom to your bountiful continent as we once brought it to Greece. Far be it from us to leave your resistance movement in the hands of the Alt-Right or comparable culturally impoverished and regressive reactionaries. We are coming to save you, America. So speaks the living spirit of Xerxes, King of Kings, Light of the Aryans...

Once again, both Johnson and Spencer think/have thought that this Jorjani is someone that needs to be seriously listened to, someone who needs to be high in WN councils.

The essential problem here, I believe, is the strong need, the strong desire, the strong craving, of the Far Right for affirmation and approval.  And when such affirmation and approval comes from someone with some sort of credentials, such as Jorjani's academic status, then the craving becomes too intense to resist.  Caution is thrown to the winds, which is one major reason that the Far Right is so easily infiltrated, betrayed, hobbled by defectives, and infested with all sorts of bizarre flotsam and jetsam.  Further, since most in the Far Right lack any sort of formal scientific training whatsoever, they are unable to distinguish between what's valuable and what's not (hint: the HBD cult falls into the latter category).  Therefore, someone with a solid scientific background would have been less apt to become impressed with Jorjani's esoteric techno-babble, and would have looked with prudent skepticism on taking anything else the fellow had to say seriously.

When oh when will the Alt Right darkness be dispelled from the land so that sane racial nationalism can come into the light?

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Wednesday, November 15, 2017

VDARE in Der News

More "movement" nonsense.


Yes, they really don’t like those red state Scotch-Irish like Barletta.  Or, if paging Roissy, Barletta is actually Amish?

Oh, well, they’re actually talking about the general population of Barletta country (which actually overlaps Biden country)? Is that it?  Many folks there are akin to Barletta and Biden themselves, ethnically speaking; you know, the ones who actually made Trump win Pennsylvania (as opposed to Roissy’s mythical wagon trains of Amish horse-and-buggies convening en masse to voting stations).




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Tuesday, November 14, 2017

A Good Podcast: 11/14/17

Transatlantic Pact.

Listen here. The best podcast of the Alt Right continues to create good material – it is not necessary to have podcasts that consist of Beavis-and-Butthead style sniggering, or cunning parasites thanking their deluded hosts (“donors”) for handing over their hard-earned shekels.

Good discussion about “Whiteness” and the balance between pan-Europeanism and nationalism. The idea that individual European ethnies cannot survive on their own, good point, and one I’ve made many times.

Perhaps normal Europeans are not contemplating war with each other, but crazed ethnonationalists sure do, with their advocacy of intra-European “ethnic cleansing.”

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Monday, November 13, 2017

A Tacit Admission That Sallis Is Right

Quota queens on parade.

I recently commented on how Der Movement’s sick embrace of the evil and anti-WN Derbyshire can be at least partially explained by the “movement’s" strict and fervent practice of affirmative action.


…it does not explain the fervor with which Derbyshire been embraced, and the alacrity by which Sallis has been, in contrast, blacklisted.  Thus, second, I must invoke the "movement's" affirmative action program.  Derbyshire - even with his Chinese family connections - is "one of the boys" so years of extreme anti-WN activism is breezily dismissed…

I didn’t think I would be proven right (again) so soon, but Der Movement never disappoints.  Thus, an activist now describes, on an Alt Right blog, meeting Derbyshire at a conference, and why it was such a big thrill; excerpts, emphasis added:


As a hopeless Anglophile, meeting John Derbyshire was a high point for me…With a glass of red wine in tow, he was most cordial and gentlemanly, a fountain of learned insight and witticisms…On the Anglophile theme, I was able to touch base with Peter Brimelow...

That’s the viciously anti-WN “latrine flies” Derbyshire and the panhandler Brimelow, who is one of several individuals primarily responsible for foisting Derbyshire on the rest of us.  But, but, but….they’re English….

Do I ever get tired of being right?  In a word: NO.


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Sunday, November 12, 2017

Genetic Detection of Immigrants

Multilocus genotypes.

Detecting immigrants from the analysis of multilocus genotypes: paper here.  An old paper; of course, methodology has gone past this since; nevertheless, it deserves to be noted, for the idea that looking at multilocus genotypes allows for distinguishing genetic types even when "bean bag genetics" differentiation is low.  The basic premise; emphasis added:

Immigration is an important force shaping the social structure, evolution, and genetics of populations. A statistical method is presented that uses multilocus genotypes to identify individuals who are immigrants, or have recent immigrant ancestry. The method is appropriate for use with allozymes, microsatellites, or restriction fragment length polymorphisms (RFLPs) and assumes linkage equilibrium among loci. Potential applications include studies of dispersal among natural populations of animals and plants, human evolutionary studies, and typing zoo animals of unknown origin (for use in captive breeding programs). The method is illustrated by analyzing RFLP genotypes in samples of humans from Australian, Japanese, New Guinean, and Senegalese populations. The test has power to detect immigrant ancestors, for these data, up to two generations in the past even though the overall differentiation of allele frequencies among populations is low.

Classical theory in population genetics has focused on the long term effects of immigration on allele frequency distributions in semi-isolated populations, concentrating on the stationary distribution resulting from a balance between forces of immigration, genetic drift, and mutation (1–4). Less theory exists addressing the effect of recent immigration among populations with low levels of genetic differentiation. A theory describing the effects of immigration on the genetic composition of individuals in populations that are not at genetic equilibrium is needed to interpret much of the data being generated using current genetic techniques. 
In this paper we consider the multilocus genotypes that result when individuals are immigrants, or have recent immigrant ancestry. We propose a test that allows recent immigrants to be identified on the basis of their multilocus genotypes; the test has considerable power for detecting immigrant individuals even when the overall level of genetic differentiation among populations is low. Molecular genetic techniques that allow multilocus genotypes to be described from single individuals are relatively new, and much of the information contained in these types of data is not fully exploited by estimators of long term gene flow that are currently available (5–7). We provide an example of an application of the method to restriction fragment length polymorphism (RFLP) genotypes from human populations; the method may also be applied to analyze multilocus allozyme and microsatellite data.
Also:

 At least three potentially misleading results may arise when applying the method considered here. First, the failure to reject the hypothesis that an individual was an immigrant, or descended from immigrants, may simply reflect the fact that the appropriate populations for comparison were not included in the analysis. Second, an individual might incorrectly appear to have originated in a particular population other than the one from which it was sampled. This might be due to similarities in allele frequencies, due to long-term gene flow, between that population and a third population from which the individual actually originated, but which was not included in the sample of populations. Third, the fact that many pairwise comparisons between populations are performed for each of a large number of individuals means that some individuals will appear to be immigrants purely by chance.

See this as well.  And also this.

In the late 1990s and early 2000s, there was some work going on in population genetics concerning multilocus genotypes.  A lot of good could have come from that if it was continued.  By an interesting coincidence, work on this subject essentially ended around the same time Der Movement and the HBDers went online talking about, and dissecting, population genetics studies.  It could be a coincidence, but given how most population geneticists are hysterical SJWs, maybe some of them decided not to investigate areas of their field that would focus attention on the great degree of actual ethnoracial differentiation that exists when genetic structure is taken into account.



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