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Simplified qpAdm plot using modern populations as sources Only samples with p > 0.01 and coverage >0.53 are shown. See also Figure S3A and Table S6.

Simplified qpAdm plot using modern populations as sources Only samples with p > 0.01 and coverage >0.53 are shown. See also Figure S3A and Table S6.

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We investigate a 2,000-year genetic transect through Scandinavia spanning the Iron Age to the present, based on 48 new and 249 published ancient genomes and genotypes from 16,638 modern individuals. We find regional variation in the timing and magnitude of gene flow from three sources: the eastern Baltic, the British-Irish Isles, and southern Europ...

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... almost identical pattern is seen for East Asian and Native American ancestry, used here as proxies of Siberian-Uralic ancestry ( Figure 6B). These were estimated with a supervised run of ADMIXTURE using five training populations from the 1000 genomes dataset (Utah residents with Northern and Western European ancestry [CEU], Indian Telugu in the UK [ITU], Han Chinese in Beijing, China [CHB], Peruvian in Lima Peru [PEL], and Yoruba in Ibadan, Nigeria [YRI]) ( Figure S4). To further explore the north-south differences, we used the first 10 PCs in a PCA based on the 16,638 modern Scandinavians ( Figure S3C) to calculate the average Euclidean PC distance between the 1,606 modern Danes and each of the 7,385 modern Norwegian and 7,647 modern Swedish individuals. ...

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During archaeological excavations at Vester Egesborg, a landing site from the Late Germanic Iron Age and Viking Age was found. The find material at the site was large and varied, providing proof of contacts with other places in the southern Baltic Sea area. This includes a significant number of sherds looking like Early Slavic Sukow pottery, which...

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... DNA molecules of Greek samples (n = 51) were extracted in the aDNA facilities at the Centre for Palaeogenetics (CPG), Stockholm University (Sweden). DNA extraction and library preparation were done as in (Rodríguez-Varela et al., 2023). Purified libraries were sequenced on NovaSeq 6000 at the SciLife Sequencing Centre in Stockholm. ...
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... Studies using Y-chromosome markers 6,7 found little evidence of an enrichment of Norse/Scandinavian haplogroups in Irish males with putatively Norse surnames while others, using genotypes from modern European populations to capture ancestry proportions population 2,3,8 , found conflicting evidence of Norwegian ancestry in the Irish population. Recently, ancient genomes from various timepoints have been used to illustrate that while there was indeed Norwegian Viking ancestry in Ireland, there was also significant gene flow from Ireland and the British Isles 9 , into Scandinavia during the Viking age 10 . However, the genetic footprints of the demographic history within the island of Ireland is relatively under-studied -there is a gap in our understanding of how the effective population size and genetic structure within regions of Ireland has changed over time. ...
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Background While subtle yet discrete clusters of genetic identity across Ireland and Britain have been identified, their demographic history is unclear. Methods Using genotype data from 6,574 individuals with associated regional Irish or British ancestry, we identified Irish-like and British-like genetic communities using network community detection. We segregated Identity-by-Descent (IBD) and Runs-of-Homozygosity (ROH) segments by length and approximated their corresponding time periods. Through this, we inferred the regional Irish and British demographic histories in these time periods by (1) estimating genetic relatedness between communities, (2) estimating changes in effective population sizes, (3) inferring recent migration rates across Ireland and Britain, and (4) estimating changing affinities to regional European populations. For a subset of the Irish communities, we determined the enrichment/depletion of surnames within the genetic communities. Results Through patterns of IBD-sharing and ROH, we find evidence of recent population bottlenecks in the Orcadian, Manx and Welsh communities. While the structure in Ireland is subtler, the communities share relatively more IBD segments that are shorter in length, and the genetic differences between the Irish communities are more subtle on average, when compared to the British communities. Regional effective population size trajectories indicate a similar demographic history throughout the island of Ireland. Further, we observe a stable migration corridor between north-east Ireland and south-west Scotland while there is a recent migration barrier between South-Eastern Ireland and Western Ireland. We observed an enrichment of Anglo-Norman and English surnames in the Wexford community while within the West Ulster-Argyll community, we saw an enrichment of Gallowglass and Scottish surnames. Conclusions Using well-annotated Irish and British reference genotypes, we observed temporal changes in genetic affinities within and between genetic communities in Ireland and Britain. In addition, using effective population size estimates and levels of haplotype-sharing, we detected varying degrees of genetic isolation in some Irish and British genetic communities across time. Using these new insights into the regional demographic history of Ireland and Britain across different time periods, we hope to understand the driving forces of rare allele frequencies and disease risk association within these populations.
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... The existence of a Christian community can be assumed, at least for the cemetery of Havor, as the discovery of a cross pendant in the grave of a male, next to that of the woman with the modified skull, suggests (Toplak 2023c:176-177, 204-205). As indicated by aDNA analyses on the two individuals from Havor and Kvie, the female from Havor was of Gotlandic origin, while the female from Kvie came from the eastern Baltic area, possibly Lithuania (Rodríguez-Varela et al. 2023). ...
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... We ran NgsRelate using BAM files as input with default parameters using a panel of 1,554,712 autosomal transversion SNPs from the Estonian Genome Diversity Project (EGDP) [31]. We calculated population allele frequencies from two different datasets of individuals from various archeological contexts in Sweden: Viking Age to Medieval dataset (n = 163) dataset covering three different sites, i.e., Sigtuna (n = 64), Fjälkinge (n = 11), and Västerhus (n = 88) [7,32], and a 17th century dataset (n = 44) [33]. All samples in the ancient reference panels were generated in a similar manner as the individuals tested here. ...
... In order to better understand previously detected kinship, we employed additional previously not used tools, KIN [8] and NgsRelate [9], to estimate the degree of relatedness and possible pedigree relationship between the two individuals. For the NgsRelate allele frequency estimation, we used various ancient genomic reference datasets, all consisting of genomic data generated from ancient samples from Sweden dated to the medieval period (n = 163) and the 17th century (n = 44) [7,32,33]. Finally, we assumed a minimum of 5000 overlapping SNPs as a cut-off value, as this has been shown to be a reliable and conservative value allowing for kinship estimation up to the third-degree [38]. Based on obtained autosomal kinship coefficients (θ) (0.09-0.15), associated k0 (0.31-0.58), k1 (0.36-0.56), and k2 (0.08-0.01) values (Tables 2 and S4), and results from KIN (Table S5), we noted that the two individuals were most probably second-degree relatives, as shown earlier [1]. ...
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Damen i Viken. En folkvandringstida kvinna från Lovö, Sverige.