First Result: Haplogroup E1b1b (North African Marker)
Haplogroup E1b1b
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Time of Origin: ~24,000–27,000 years ago
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Place of Origin: East Africa or the Levant
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Description:
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The third most common haplogroup in Europe
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Widespread among North African and Southwest Asian populations
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A foundational lineage of the North Africans (Maghrebi and Egyptians) populations
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What Is a Short Tandem Repeat (STR)?
A Short Tandem Repeat (STR) is a short DNA sequence (usually 2–6 base pairs) that is repeated several times in a row at a specific location on the Y chromosome.
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Example: At a marker like DYS393, the sequence "AGAT" might be repeated 13 times:
AGATAGATAGAT...→ 13 repeats = value 13 -
Each marker (DYS456, DYS390, etc.) has a different repeat unit and location.
STRs mutate relatively quickly (every few hundred generations), so:
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They are useful for recent ancestry and relationship testing
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But they are not reliable for deep evolutionary trees
SNPs (Single Nucleotide Polymorphisms):
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A single-letter mutation (like A → G) at a specific base-pair position
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Occur very rarely and are stable over thousands of years
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Used to define haplogroups and their branches.
Main Subclades of E1b1b: M81, M78, and V13
These are the names of SNP mutations that define subclades of E1b1b:
| Subclade | SNP Defining It | Approximate Age | Notes |
|---|---|---|---|
| E-M81 | Mutation M81 | ~5,600–7,000 ybp | Common in North Africa (Berbers) |
| E-M78 | Mutation M78 | ~12,000–14,000 ybp | Nile Valley, East Africa, also Europe |
| E-V13 | Mutation V13 | ~5,000–7,000 ybp | Balkans and Mediterranean Europe |
Estimated Subclade Probabilities (based on STR profile by ChatGPT)
| Subclade | STR Match Probability | Notes |
|---|---|---|
| E-M81 | ~95–98% | Classic North African (Berber) pattern: 13–24–14–11–13 is textbook E-M81. Your profile fits like a glove. |
| E-M78 | ~1–3% | Some overlap, but key markers (e.g. DYS391 = 9, DYS458 = 18) make this unlikely |
| E-V13 | <1% | Values like DYS456 = 15 and DYS391 = 9 do not support Balkan pattern |
NevGen Predictor
NevGen is a widely used predictor that builds on the Bayesian approach, enhanced by:
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Empirical allele frequencies per subclade (e.g. E‑M81, E‑M78, E‑V13)
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STR marker correlations (for example, how DYS390 = 24 correlates with DYS391 = 9 within subclades)
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It limits over-counting by using at most two correlated values per marker and prefers negative correlations to refine predictions
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The web version uses data sets of 17 or 23 STR markers and outputs probabilities and "fitness" scores in batch mode
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NevGen’s accuracy has been tested extensively:
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Simulated “descendant” haplotypes across 40 generations were used to test prediction performance.
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On ~67 markers, accuracy is around 89%, and on full 111-marker profiles, ~97% on original samples, slightly lower on simulated ones
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These tests validate that if a predicted haplogroup receives >80% probability, it's almost always correct
Second Result: E-M81 Subclade (Berber-Maghrebi Marker)

Fitness score measures how closely the STR values match the known STR signature for that subclade.
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It’s a quantitative match score, usually ranging from 0 to 100
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Higher fitness = closer genetic fit
In summary, I belong to haplogroup E-M81 (defined by V257 > M81):
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Origin: ~5,600–7,000 years ago (Copper Age)
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Location: Almost certainly North Africa, especially the Maghreb
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Expansion: Rapid population growth and expansion around Neolithic–Chalcolithic transition, coinciding with Berberization of the region
From here, the line split into several downstream clades like PF2546, M299, BY45625, Z5009, etc.
Third Result: E-M81- PF2548 (Numidian Marker)
E-M81 is a broad clade with many sub-branches, formed by additional SNP mutations over the past ~5,000–7,000 years.
I am not just E-M81, but specifically:
→ PF2548 → PF2546 → M299So:
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E-M81 is the parent clade
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PF2546 is a major downstream branch
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M299 is (the dominant) terminal branch, i.e., a currently known end-point in the phylogenetic tree for your sample
The M299 has a probability of 29 %. The PF2546 branch itself is confirmed with a probability of about 45 %, while a 20 % probability is carried by the subclade A5604. In other words, roughly 35 % of the result falls into the category of “unsupported subclade.”
All these results so far are obtained with “No known SNP” selected.
When the SNP is set to Z827, L19, or M81, the “unsupported subclade” probability drops to 16 %, with 54 % assigned to A5604—a subclade of PF2548, which is itself upstream of PF2546. This later subcladed carries now a probability of 30 %. In this case we have:
PF2548 vs. E-M81
E-M81: The North African / Berber Marker
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Time Depth: ~5,600–7,000 ybp
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Origin: Early Neolithic North Africa
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Spread: Broad Maghreb — Morocco, Algeria, Tunisia, Libya
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Role: Signature of the Berber ethnogenesis, including Capsian–Neolithic fusion and pre-linguistic population unification
🟩 It marks the entire Berber population layer, from prehistoric pastoralists to modern Imazighen.
PF2548: The Numidian Marker (A Sub-Berber Lineage)
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Time Depth: ~2,800–3,000 ybp
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Origin: Tell Atlas zone (likely north-central Algeria)
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Spread: Concentrated in Algeria and Tunisia
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Role: Signature of Iron Age tribal consolidation — i.e., Numidian-Berber state formation
🟨 It marks the formation of settled tribal Numidian culture and kingdoms.



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