The Neanderthal population history and the introgression landscape inferred from the UK Biobank

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The paper studied the population history and genomic landscape of Neanderthal introgression in present-day Eurasians by analyzing Neanderthal haplotypes across 45,000 imputed and phased UK Biobank genomes. Using the allele frequency spectrum within surviving Neanderthal segments, the authors inferred a divergence time of 2,061 generations between the introgressed lineage and the Vindija Neanderthal and estimated the introgressed lineage’s effective population size to be Ne = 6,564, while also observing uneven genomic distribution into introgression deserts and high-frequency segments consistent with adaptive introgression plus drift. At the individual level, they identified 545 independent loci with excess Neanderthal homozygosity, interpreted as consistent with ongoing selection, and detected seven Human Accelerated Regions influenced by recent selective sweeps, with four located in introns of cerebellum-expressed genes. A stated limitation is that saturation of overlapping haplotypes was not reached and rare haplotypes still appear even at this scale. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Neanderthal haplotypes in present-day Eurasians are unevenly distributed across the genome, forming introgression deserts and high-frequency segments consistent with adaptive introgression, with additional random variation affected by genetic drift. However, current estimates are limited by modest sample sizes and analyses restricted to subsets of the genome, given that any individual carries only 1-2% Neanderthal ancestry. Here we extract and analyse Neanderthal haplotypes from 45,000 imputed and phased genomes in the UK Biobank. Even at this scale, the number of sites overlapping Neanderthal haplotypes approaches—but does not reach—saturation, with rare haplotypes still being discovered. Using the derived allele frequency spectrum within the surviving Neanderthal segments, we infer a divergence time of 2,061 generations between the introgressed lineage and the Vindija Neanderthal, and estimate the effective population size of the introgressed lineage to Ne = 6,564. Individual-level resolution allows identification of 545 independent loci with excess Neanderthal homozygosity, consistent with ongoing selection. Despite the extensive dataset, a substantial portion of the genome remains a Neanderthal desert. Within these regions, we detect seven Human Accelerated Regions affected by recent human selective sweeps (TMRCA <650 kya), four located within introns of cerebellum-expressed genes, providing further support for their potential as modern human-specific adaptation.
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Abstract Neanderthal haplotypes in present-day Eurasians are unevenly distributed across the genome, forming introgression deserts and high-frequency segments consistent with adaptive introgression, with additional random variation affected by genetic drift. However, current estimates are limited by modest sample sizes and analyses restricted to subsets of the genome, given that any individual carries only 1-2% Neanderthal ancestry. Here we extract and analyse Neanderthal haplotypes from 45,000 imputed and phased genomes in the UK Biobank. Even at this scale, the number of sites overlapping Neanderthal haplotypes approaches—but does not reach—saturation, with rare haplotypes still being discovered. Using the derived allele frequency spectrum within the surviving Neanderthal segments, we infer a divergence time of 2,061 generations between the introgressed lineage and the Vindija Neanderthal, and estimate the effective population size of the introgressed lineage to Ne = 6,564. Individual-level resolution allows identification of 545 independent loci with excess Neanderthal homozygosity, consistent with ongoing selection. Despite the extensive dataset, a substantial portion of the genome remains a Neanderthal desert. Within these regions, we detect seven Human Accelerated Regions affected by recent human selective sweeps (TMRCA <650 kya), four located within introns of cerebellum-expressed genes, providing further support for their potential as modern human-specific adaptation. Competing Interest Statement The authors have declared no competing interest.

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