Published January 6, 2026
| Version v1
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Genomic Synteny and the Empirical Invalidation of Y-Chromosomal Bifurcation Models in Levantine Populations
Authors/Creators
- 1. Independent Forensic Genomics Researcher; Stanford University School of Medicine, Department of Genetics (Certificate, 2024)
Description
Description
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This study presents high-resolution raw genomic data (Build 37.1) demonstrating multi-clade synteny on the human Y-chromosome. The co-occurrence of derived states for J-Parent (M304), J1 (M267), J2 (M172), and G (M201) markers on a basal E-M329/V38 backbone suggests current phylogenetic partitions are artifactual. Statistical analysis yields P < 10⁻¹⁵ under bifurcation models, necessitating re-evaluation of Levantine population genetics.
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d31f390981678d008f0fd8728f0c234158a824b26c53f385223d8002edd0cb96
Raw genomic data available upon request for verification.
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synteny_main_v1_draft_clean.pdf
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Additional details
Dates
- Submitted
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2026-01-06This study presents high-resolution raw genomic data (Build 37.1) demonstrating multi-clade synteny on the human Y-chromosome. The co-occurrence of derived states for J-Parent (M304), J1 (M267), J2 (M172), and G (M201) markers on a basal E-M329/V38 backbone suggests current phylogenetic partitions are artifactual. Statistical analysis yields P < 10⁻¹⁵ under bifurcation models, necessitating re-evaluation of Levantine population genetics.