September 10, 2014

ASHG 2014 titles and abstracts

Some interesting titles from the ASHG 2014 conference.

UPDATE: I have added the abstracts.

The human X chromosome is the target of megabase wide selective sweeps associated with multi-copy genes expressed in male meiosis and involved in reproductive isolation. M. H. Schierup, K. Munch, K. Nam, T. Mailund, J. Y. Dutheil.
   The X chromosome differs from the autosomes in its hemizogosity in males and in its intimate relationship with the very different Y chromosome. It has a different gene content than autosomes and undergo specific processes such as meiotic sex chromosome inactivation (MSCI) and XY body formation. Previous studies have shown that natural selection is more efficient against deleterious mutations and, in chimpanzee, that positive selection is prevalent. We show that in all great apes species, megabase wide regions of the X chromosome has severely reduced diversity (by more than 80%). These regions are partly shared among species and indicate a large number of strong selective sweeps that have occurred independently on the same set of targets in different great apes species. We use simulations and deterministic calculations to show that background selection or soft selective sweeps are unlikely to be responsible. The regions also bear all the hallmarks of selective sweeps such as an increased proportion of singletons and higher divergence among closely related populations. Human populations are differently affected, suggesting that a large fraction of sweeps are private to specific human populations. The regions of reduced diversity correlates strongly with the position of X-ampliconic regions, which are 100-500 kb regions containing multiple copies of genes that are solely expressed during male meiosis. We propose that the genes in these regions escape MSCI and participate in an intragenomic conflict with regions of similar function on the Y chromosome for transmission of sex chromosomes to the next generation, i.e. sex chromosome meiotic drive. Recent results from Neanderthal introgression into humans point to the same regions as showing no introgression, consistent with the above process leading to reproductive isolation. Strikingly, the same regions of the X also shows much reduced divergence between human and chimpanzee, suggesting either that this speciation process was indeed complex or that the same regions were under strong selection in the human chimpanzee ancestor.
New insights on human de novo mutation rate and parental age. W. S. W. Wong, B. Solomon, D. Bodian, D. Thach, R. Iyer, J. Vockley, J. Niederhuber.
 Germline mutations have a major role to play in evolution. Much attention has been given to studying the pattern and rate of human mutations using biochemical or phylogenetic methods based on closely related species. Massively parallel sequencing technologies have given scientists the opportunity to study directly measured de novo mutations (DNMs) at an unprecedented scale. Here we report the largest study (to our knowledge) of de novo point mutations in humans, in which we used whole genome deep sequencing (~60x) data from 605 family trios (father, mother and newborn). These trios represent the first group of approximately 2,700 trios who have undergone whole-genome sequencing (WGS) through our pediatric-based WGS research studies. The fathers ages range from 17 to 63 years and the mothers ages range from 17 to 43 years. We identified over 23000 DNMs (~40 per newborn) in the autosomal chromosomes using a customized pipeline and infer that the mutation rate per basepair is around 1.2x10-8 per generation, well within the reported range in previous studies. We were also able to confirm that the total number of DNMs in the newborn was directly proportional to the paternal age (P  less than 2x10-16). Maternal age is shown to have a small but significant positive effect on the number of DNMs passed onto the offspring, (P =0.003) , even after accounting for the paternal age. This contradicts the prior dogma that maternal age only has an effect on chromosomal abnormalities related to nondisjunction events. Furthermore, 5% (22 total) of newborns in the analyzed group were conceived with assisted reproductive technologies (ARTs), and these infants have on average 5 more DNMs (Bias corrected and accelerated bootstrap 95% Confidence Interval, 1.24 to 8.00) than those conceived naturally, after controlling for both parents ages. Both parents ages remain significant as independently correlated with DNMs even after the families that used ARTs were removed from the analysis. Our study enhances current knowledge related to the human germline mutational rates.
Alignment to an ancestry specific reference genome discovers additional variants among 1000 Genomes ASW Cohort. R. A. Neff, J. Vargas, G. H. Gibbons, A. R. Davis.
   Whole genome sequencing studies across certain populations, such as those with African ancestry, are often underpowered due to a larger divergence between the common reference genome and the true genetic sequence of the population. However, a common reference genome is not designed to account for this divergence in population-specific studies. Strong signals from common (MAF>50%) single nucleotide polymorphisms (SNPs), insertion-deletions (indels), and structural variants (SVs) can make alignment and variant calling difficult by masking nearby variants with weaker genetic signals. We present the results generated from alignment to an African descent population-specific reference genome by applying variants present in a majority of individuals with African descent from all phases of the 1000 Genomes Project and the International HapMap Consortium. We identified 882,826 single nucleotide polymorphisms, short insertion-deletion events, and large structural variations present at MAF>50%; in the population, representing 2.39 MB of genetic variation changed from hg19. We demonstrate that utilization of a population-specific reference improves variant call quality, coverage level, and imputation accuracy. We compared alignment of 27 African-American SW population (ASW) samples from the 1000 Genomes Phase 1 project between the population-specific and the hg19 reference. We discovered an additional 443,036 SNPs by alignment to the population specific reference in union across all samples, including thousands of exonic variants that are non-synonymous and are clinically relevant to the study of disease.
Using compressed data structures to capture variation in thousands of human genomes. S. A. McCarthy, Z. Lui, J. T. Simpson, Z. Iqbal, T. M. Keane, R. Durbin.
   Currently the most widely used approach to catalogue variation amongst a set of samples is to align the sequencing reads to a single linear reference genome. This principle has been at the core of the 1000 Genomes data processing pipeline since the pilot phase of the project. However, there is now an increased awareness of the limitations of this approach, such as alignment artefacts, reference bias and unobserved variation on non-reference haplotypes. The Burrows-Wheeler transform and FM-index are compact data structures that have been successfully used in sequence alignment and assembly. One of the key features of these structures is that they are a searchable and reference-free representation of the raw sequencing reads. Our project aims to build a web server based on BWT data structures containing all the reads from many thousands of samples so as to efficiently retrieve matching reads and information about samples and populations. Enticingly, it is expected that data storage for this system would plateau as we collect more data since most new sequencing reads will have already been observed. We expect this to enable powerful new ways to query variation data from thousands of individuals. For the first phase of this project, we include all 87 Tbp of the low-coverage and exome data from the 2,535 samples in 1000 Genomes Phase 3. We envisage this would provide a means for researchers to easily check the prevalence of any human sequence in a control set of thousands of putatively healthy samples. We present our approaches and initial benchmarks on variant sensitivity and specificity against truth datasets and explore several applications for these structures such as validation of short insertion/deletion and structural variant calls, and rapid searching for traces of viral DNA.
Second-generation PLINK: Rising to the challenge of larger and richer datasets. C. C. Chang, C. C. Chow, L. C. A. M. Tellier, S. Vattikuti, S. M. Purcell, J. J. Lee.
   PLINK 1 is a widely used open-source C/C++ toolset for genome-wide association studies (GWAS) and research in population genetics. However, the steady accumulation of data from imputation and whole-genome sequencing studies has exposed a strong need for even faster and more scalable implementations of key functions. In addition, GWAS and population-genetic data now frequently contain probabilistic calls, phase information, and/or multiallelic variants, none of which can be represented by PLINK 1's primary data format.    To address these issues, we are developing a second-generation codebase for PLINK. The first major release from this codebase, PLINK 1.9, introduces extensive use of bit-level parallelism, O(sqrt(n))-time/constant-space Hardy-Weinberg equilibrium and Fisher's exact tests, and many other algorithmic improvements. In combination, these changes accelerate most operations by 1-4 orders of magnitude, and allow the program to handle datasets too large to fit in RAM. This will be followed by PLINK 2.0, which will introduce (a) a new data format capable of efficiently representing probabilities, phase, and multiallelic variants, and (b) extensions of many functions to account for the new types of information.    The second-generation versions of PLINK will offer dramatic improvements in performance and compatibility. For the first time, users without access to high-end computing resources can perform several essential analyses of the feature-rich and very large genetic datasets coming into use.
Exploring genetic variation and genotypes among millions of genomes. R. M. Layer, A. R. Quinlann.
Integrated analysis of protein-coding variation in over 90,000 individuals from exome sequencing data. D. G. MacArthur, M. Lek, E. Banks, R. Poplin, T. Fennell, K. Samocha, B. Thomas, K. Karczewski, S. Purcell, P. Sullivan, S. Kathiresan, M. I. McCarthy, M. Boehnke, S. Gabriel, D. M. Altshuler, G. Getz, M. J. Daly, Exome Aggregation Consortium.
   Rare, and thus largely unknown, variants are a major reason that, typically, less than 10% of the heritability of complex diseases currently can be explained by known genetic variation. While increasing the number of sequenced genomes may improve our ability to reveal this “hidden heritability,” the scale of the resulting dataset poses substantial storage and computational demands. Current efforts to sequence 100,000 genomes, and combined efforts that are likely to surpass 1 million genomes will identify hundreds of millions to billions of polymorphic loci. The minimum storage requirement for directly representing the variability found by these projects (1 bit per individual per variant, ignoring the necessary metadata) will range from terabytes to petabytes. Like most big-data problems, a balance must be found between optimizing storage and computational efficiency. For example, while compression can minimize storage by reducing file size, it can also cause inefficient computation since data must be decompressed before it can be analyzed. Conversely, highly structured data can reduce analysis times but typically require extra metadata that increase file size. Current variation storage schemes were not designed to quickly analyze massive datasets and fail to balance these competing goals. We present GENOTQ, an open source API and toolkit that reduces file size and data access time through use of a succinct data structure, a class of data structures that compress data such that operations can be performed without requiring the full decompression. Word aligned hybrid (WAH) bitmap compression is one such data structure that was developed to improve query times for relational databases. Binary values are encoded such that logical operations (AND, OR, NOT) can be performed on the compressed data. This encoding results in file sizes that are 20X smaller than uncompressed versions, and only 50% larger than the compressed version. Queries, such as finding shared variants among a subpopulation, are also 21X faster. Furthermore, representing the genotypes in this manner makes our method well suited to both distributed architectures like BigQuery and parallel processors like GPUs. We stress that this method is only part of a larger solution that would incorporate genomic annotations, medical histories, and pedigrees. Incorporating fast genotype queries with this web of metadata will provide a rich information source to both clinicians and researchers.
Capture of 390,000 SNPs in dozens of ancient central Europeans reveals a population turnover in Europe thousands of years after the advent of farming. I. Lazaridis, W. Haak, N. Patterson, N. Rohland, S. Mallick, B. Llamas, S. Nordenfelt, E. Harney, A. Cooper, K. W. Alt, D. Reich.
   To understand the population transformations that took place in Europe since the early Neolithic, we used a DNA capture technique to obtain reads covering ~390 thousand single nucleotide polymorphisms (SNPs) from a number of different archaeological cultures of central Europe (Germany and Hungary). The samples spanned the time period from 7,500 BP to 3,500 BP (Early Neolithic to Early Bronze Age periods) and most of them were previously studied using mtDNA (Brandt, Haak et al., Science, 2013). The captured SNPs include about 360,000 SNPs from the Affymetrix Human Origins Array that were discovered in African individuals, as well as about 30,000 SNPs chosen for other reasons (that are thought to have been affected by natural selection, or to have phenotypic effects, or are useful in determining Y-chromosome haplogroups). By analyzing this data together with a dataset of 2,345 present-day humans and other published ancient genomes, we show that late Neolithic inhabitants of central Europe belonging to the Corded Ware culture were not a continuation of the earlier occupants of the region. Our results highlight the importance of migration and major population turnover in Europe long after the arrival of farming. * Contributed equally to this work.
Insights into British and European population history from ancient DNA sequencing of Iron Age and Anglo-Saxon samples from Hinxton, England. S. Schiffels, W. Haak, B. Llamas, E. Popescu, L. Loe, R. Clarke, A. Lyons, P. Paajanen, D. Sayer, R. Mortimer, C. Tyler-Smith, A. Cooper, R. Durbin.
   British population history is shaped by a complex series of repeated immigration periods and associated changes in population structure. It is an open question however, to what extent each of these changes is reflected in the genetic ancestry of the current British population. Here we use ancient DNA sequencing to help address that question. We present whole genome sequences generated from five individuals that were found in archaeological excavations at the Wellcome Trust Genome Campus near Cambridge (UK), two of which are dated to around 2,000 years before present (Iron Age), and three to around 1,300 years before present (Anglo-Saxon period). Good preservation status allowed us to generate one high coverage sequence (12x) from an Iron Age individual, and four low coverage sequences (1x-4x) from the other samples.   By providing the first ancient whole genome sequences from Britain, we get a unique picture of the ancestral populations in Britain before and after the Anglo-Saxon immigrations. We use modern genetic reference panels such as the 1000 Genomes Project to examine the relationship of these ancient samples with present day population genetic data. Results from principal component analysis suggest that all samples fall consistently within the broader Northern European context, which is also consistent with mtDNA haplogroups. In addition, we obtain a finer structural genetic classification from rare genetic variants and haplotype based methods such as FineStructure. Reflecting more recent genetic ancestry, results from these methods suggest significant differences between the Iron Age and the Anglo-Saxon period samples when compared to other European samples. We find in particular that while the Anglo-Saxon samples resemble more closely the modern British population than the earlier samples, the Iron Age samples share more low frequency variation than the later ones with present day samples from southern Europe, in particular Spain (1000GP IBS). In addition the Anglo-Saxon period samples appear to share a stronger older component with Finnish (1000GP FIN) individuals. Our findings help characterize the ancestral European populations involved in major European migration movements into Britain in the last 2,000 years and thus provide more insights into the genetic history of people in northern Europe.
Fine-scale population structure in Europe. S. Leslie, G. Hellenthal, S. Myers, P. Donnelly, International Multiple Sclerosis Genetics Consortium.
   There is considerable interest in detecting and interpreting fine-scale population structure in Europe: as a signature of major events in the history of the populations of Europe, and because of the effect undetected population structure may have on disease association studies. Population structure appears to have been a minor concern for most of the recent generation of genome-wide association studies, but is likely to be important for the next generation of studies seeking associations to rare variants. Thus far, genetic studies across Europe have been limited to a small number of markers, or to methods that do not specifically account for the correlation structure in the genome due to linkage disequilibrium. Consequently, these studies were unable to group samples into clusters of similar ancestry on a fine (within country) scale with any confidence. We describe an analysis of fine-scale population structure using genome-wide SNP data on 6,209 individuals, sampled mostly from Western Europe. Using a recently published clustering algorithm (fineSTRUCTURE), adapted for specific aspects of our analysis, the samples were clustered purely as a function of genetic similarity, without reference to their known sampling locations. When plotted on a map of Europe one observes a striking association between the inferred clusters and geography. Interestingly, for the most part modern country boundaries are significant i.e. we see clear evidence of clusters that exclusively contain samples from a single country. At a high level we see: the Finns are the most differentiated from the rest of Europe (as might be expected); a clear divide between Sweden/Norway and the rest of Europe (including Denmark); and an obvious distinction between southern and northern Europe. We also observe considerable structure within countries on a hitherto unseen fine-scale - for example genetically distinct groups are detected along the coast of Norway. Using novel techniques we perform further analyses to examine the genetic relationships between the inferred clusters. We interpret our results with respect to geographic and linguistic divisions, as well as the historical and archaeological record. We believe this is the largest detailed analysis of very fine-scale human genetic structure and its origin within Europe. Crucial to these findings has been an approach to analysis that accounts for linkage disequilibrium.
The population structure and demographic history of Sardinia in relationship to neighboring populations. J. Novembre, C. Chiang, J. Marcus, C. Sidore, M. Zoledziewska, M. Steri, H. Al-asadi, G. Abecasis, D. Schlessinger, F. Cucca.
   Numerous studies have made clear that Sardinian populations are relatively isolated genetically from other populations of the Mediterranean, and more recently, intriguing connections between Sardinian ancestry and early Neolithic ancient DNA samples have been made. In this study, we analyze a whole-genome low-coverage sequencing dataset from 2120 Sardinians to more fully characterize patterns of genetic diversity in Sardinia. The study contains one subsample that contains individuals from across Sardinia and a second subsample that samples 4 villages from the more isolated Ogliastra region. We also merge the data with published reference data from Europe and North Africa. Overall Fst values of Sardinia to other European populations are low (less than 0.015); however using a novel method for visualizing genetic differentiation on a geographic map, we formally show how Sardinia is more differentiated than would be expected given its geographic distance from the mainland, consistent with periods of isolation. Applications of the software Admixture show how Sardinia populations differ in the levels of recent admixture with mainland European populations and that there are only minor contributions from North African populations to Sardinian ancestry. Notably the Sardinians from Ogliastra contain a distinct genetic cluster with minimal evidence of recent admixture with mainland Europe. We found frequency-based f3 tests and the tree-based algorithm Treemix both also show minimal evidence of recent admixture. Given the relative isolation, one might expect to see a unique demographic history from neighboring populations. Using coalescent-based approaches, we find Sardinian populations have had more constant effective sizes over the past several thousand years than mainland European populations, which typically show evidence for rapid growth trajectories in the recent past. This unique demographic history has consequences for the abundance of putatively damaging and deleterious variants, and we use our data to address the prediction that the genetic architecture of disease traits is expected to involve fewer loci with a greater proportion of variants at common frequencies in Sardinia.
Population structure in African-Americans. S. Gravel, M. Barakatt, B. Maples, M. Aldrich, E. E. Kenny, C. D. Bustamante, S. Baharian.
   We present a detailed population genetic study of 4 African-American cohorts comprising over 6000 genotyped individuals across US urban and rural communities: two nation-wide longitudinal cohorts, one biobank cohort, and the 1000 genomes ASW cohort. Ancestry analysis reveals a uniform breakdown of continental ancestry proportions across regions and urban/rural status, with 79% African, 19% European, and 1.5% Native American/Asian ancestries, with substantial between-individual variation. The Native Ancestry proportion is higher than previous estimates and is maintained after self-identified hispanics and individuals with substantial inferred Spanish ancestry are removed. This strongly supports direct admixture between Native Americans and African Americans on US territory, and linkage patterns suggest contact early after African-American arrival to the Americas. Local ancestry patterns and variation in ancestry proportions across individuals are broadly consistent with a single African-American population model with early Native American admixture and ongoing European gene flow in the South. The size and broad geographic sampling of our cohorts enables detailed analysis the geographic and cultural determinants of finer-scale population structure. Recent Identity-by-descent analysis reveals fine-scale structure consistent with the routes used during slavery and in the great African-American migrations of the twentieth century: east-to-west migrations in the south, and distinct south-to-north migrations into New England and the Midwest. These migrations follow transit routes available at the time, and are in stark contrast with European-American relatedness patterns.
Genetic testing of 400,000 individuals reveals the geography of ancestry in the United States. Y. Wang, J. M. Granka, J. K. Byrnes, M. J. Barber, K. Noto, R. E. Curtis, N. M. Natalie, C. A. Ball, K. G. Chahine.
   The population of the United States is formed by the interplay of immigration, migration and admixture. Recent research (R. Sebro et al., ASHG 2013) has shed light on the U.S. demography by studying the self-reported ethnicity from the 2010 U.S. Census. However, self-reported ethnicity may not accurately represent true genetic ancestry and may therefore introduce unknown biases. Since launching its DNA service in May 2012, AncestryDNA has genotyped over 400, 000 individuals from the United States. Leveraging this huge volume of DNA data, we conducted a large-scale survey of the ancestry of the United States. We predicted genetic ethnicity for each individual, relying on a rigorously curated reference panel of 3,000 single-origin individuals. Combining that with birth locations, we explored how various ethnicities are distributed across the United States Our results reveal a distinct spatial distribution for each ethnicity. For example, we found that individuals from Massachusetts have the highest proportion of Irish genetic ancestry and individuals from New York have the highest proportion of Southern European genetic ancestry, indicating their unique immigration and migration histories. We also performed pairwise IBD analysis on the entire sample set and identified over 300 million shared genomic segments among all 400,000 individuals. From this data, we calculated the average amount of sharing for pairs of individuals born within the same state or from two different states. In general, we found the genetic sharing decreases as the geographic distance between two states increases. However, the pattern also varies substantially among the 50 states. In summary, our analysis has provided significant insight on the biogeographic patterns of the ancestry in the United States.
Statistical inference of archaic introgression and natural selection in Central African Pygmies. P. Hsieh, J. D. Wall, J. Lachance, S. A. Tishkoff, R. N. Gutenkunst, M. F. Hammer.
   Recent evidence from ancient DNA studies suggests that genetic material introgressed from archaic forms of Homo, such as Neanderthals and Denisovans, into the ancestors of contemporary non-African populations. These findings also imply that hybridization may have given rise to some of adaptive novelties in anatomically modern humans (AMH) as they expanded from Africa into various ecological niches in Eurasia. Within Africa, fossil evidence suggests that AMH and a variety of archaic forms coexisted for much of the last 200,000 years. Here we present preliminary results leveraging high quality whole-genome data (>60X coverage) for three contemporary sub-Saharan African populations (Biaka, Baka, and Yoruba) from Central and West Africa to test for archaic admixture. With the current lack of African ancient DNA, especially in Central Africa due to its rainforest environment, our statistical inference approach provides an alternative means to understand the complex evolutionary dynamics among groups of the genus Homo. To identify candidate introgressive loci, we scan the genomes of 16 individuals and calculate S*, a summary statistic that was specifically designed by one of us (JDW) to detect archaic admixture. The significance of each candidate is assessed through extensive whole-genome level simulations using demographic parameters estimated by ∂a∂i to obtain a parametric distribution of S* values under the null hypothesis of no archaic introgression. As a complementary approach, top candidates are also examined by an approximate-likelihood computation method. The admixture time for each individual introgressive variant is inferred by estimating the decay of the genetic length of the diverged haplotype as a function of its underlying recombination rate. A neutrality test that controls for demography is performed for each candidate to test the hypothesis that introgressive variants rose to high frequency due to positive directional selection. Several genomic regions were identified by both selection and introgression scans, and we will discuss the possible genetic and functional properties of these “double-hits”. The present study represents one of the most comprehensive genomic surveys to date for evidence of archaic introgression to anatomically modern humans in Africa.
Inferences about human history and natural selection from 280 complete genome sequences from 135 diverse populations. S. Mallick, D. Reich, Simons Genome Diversity Project Consortium.
   The most powerful way to study population history and natural selection is to analyze whole genome sequences, which contain all the variation that exists in each individual. To date, genome-wide studies of history and selection have primarily analyzed data from single nucleotide polymorphism (SNP) arrays which are biased by the choice of which SNPs to include. Alternatively they have analyzed sequence data that have been generated as part of medical genetic studies from populations with large census sizes, and thus do not capture the full scope of human genetic variation. Here we report high quality genome sequences (~40x average) from 280 individuals from 135 worldwide populations, including 45 Africans, 26 Native Americans, 27 Central Asians or Siberians, 46 East Asians, 25 Oceanians, 46 South Asians, and 71 West Eurasians. All samples were sequenced using an identical protocol at the same facility (Illumina Ltd.). We modified standard pipelines to eliminate biases that might confound population genetic studies. We report novel inferences, as well as a high resolution map that shows where archaic ancestry (Neanderthal and Denisovan) is distributed throughout the world. We compare and contrast the genomic landscape of the Denisovan introgression into mainland Eurasians to that in island Southeast Asians. We are making this dataset fully available on Amazon Web Services as a resource to the community, coincident with the American Society of Human Genetics meeting.
Improved haplotype phasing using identity by descent. B. L. Browning, S. R. Browning.
   We present a new haplotype phasing method that achieves higher accuracy than existing methods. The method is based on the Beagle haplotype frequency model, but unlike the original Beagle phasing method, the new method incorporates genetic recombination, genotype error, and segments of identity by descent.     We compared the new haplotype phasing method to Beagle (r1230) and to SHAPEIT version 2 (r778) using Illumina Human 1M SNP data for chromosome 20. We phased 44 HapMap3 CEU trio offspring together with subsets of Wellcome Trust Case Control Consortium 2 controls (n=650, 1300, 2600, 5200). Phase error was measured at trio offspring genotypes on chromosome 20 that have phase determined by parental genotypes. The SHAPEIT “states” parameter was set at 6400 in order to increase its phasing accuracy.     The new haplotype phasing method produced haplotype switch error rates that were 20-25% lower than the error rates for the existing Beagle method and 1-7% lower than the error rates for SHAPEIT. The difference in switch error rates between the new method and SHAPEIT increased with increasing sample size.     The new haplotype phasing method will be incorporated into version 4 of the Beagle software package (
Reducing pervasive false positive identical-by-descent segments detected by large-scale pedigree analysis. E. Y. Durand, N. Eriksson, C. Y. McLean.
   Analysis of genomic segments shared identical-by-descent (IBD) between individuals is fundamental to many genetic applications, from demographic inference to estimating the heritability of diseases. A large number of methods to detect IBD segments have been developed recently. However, IBD detection accuracy in non-simulated data is largely unknown. In principle, it can be evaluated using known pedigrees, as IBD segments are by definition inherited without recombination down a family tree. We extracted 25,432 genotyped European individuals containing 2,952 father-mother-child trios from the 23andMe, Inc. dataset. We then used GERMLINE, a widely used IBD detection method, to detect IBD segments within this cohort. Exploiting known familial relationships, we identified a false positive rate over 67% for 2-4 centiMorgan (cM) segments, in sharp contrast with accuracies reported in simulated data at these sizes. We show that nearly all false positives arise due to allowing switch errors between haplotypes when detecting IBD, a necessity for retrieving long (> 6 cM) segments in the presence of imperfect phasing. We introduce HaploScore, a novel, computationally efficient metric that enables detection and filtering of false positive IBD segments on population-scale datasets. HaploScore scores IBD segments proportional to the number of switch errors they contain. Thus, it enables filtering of spurious segments reported due to GERMLINE being overly permissive to imperfect phasing. We replicate the false IBD findings and demonstrate the generalizability of HaploScore to alternative genotyping arrays using an independent cohort of 555 European individuals from the 1000 Genomes project. HaploScore can be readily adapted to improve the accuracy of segments reported by any IBD detection method, provided that estimates of the genotyping error rate and switch error rate are available.
Parente2: A fast and accurate method for detecting identity by descent. S. Bercovici, J. M. Rodriguez, L. Huang, S. Batzoglou.
   Identity-by-descent (IBD) inference is the problem of establishing a direct and explicit genetic connection between two individuals through a genomic segment that is inherited by both individuals from a recent common ancestor. IBD inference is key to a variety of population genomic studies, ranging from demographic studies to linking genomic variation with phenotype and disease. The problem of both accurate and efficient IBD detection has become increasingly challenging with the availability of large collections of human genotypes and genomes: given a cohort’s size, as quadratic number of pairwise genome comparisons must be performed, in principle. Therefore, computation time and the false discovery rate can also scale quadratically. To enable practical large-scale IBD detection, we developed Parente2, a novel method for detecting IBD segments. Parente2 is based on an embedded log-likelihood ratio and uses an ensemble windowing approach to model complex linkage disequilibrium in the underlying studied population. Parente2 is applied directly on genotype data without the need to phase data prior to IBD inference. Through extensive simulations using real data, we evaluate Parente2’s performance. We show that Parente2 is superior to previous state-of-the-art methods, detecting pairs of related individuals sharing a 4 cM IBD segment with 99.9%; sensitivity at a 0.1%; false positive rate, and achieving 79.2%; sensitivity at a 1%; false positive rate for the more challenging case of pairs sharing a 2 cM IBD segment. Additionally, Parente2 is efficient, providing one to two orders of magnitude speedup compared to previous state of the art methods. Parente2 is freely available at
Fast PCA of very large samples in linear time. K. J. Galinsky, P. Loh, G. Bhatia, S. Georgiev, S. Mukherjee, N. J. Patterson, A. L. Price.
   Principal components analysis (PCA) is an effective tool for inferring population structure and correcting for population stratification in genetic data. Traditionally, PCA runs in O(MN2+N3 ) time, where M is the number of variants and N is the number of samples. Here, we describe a new algorithm, fastpca, for approximating the top K PCs that runs in time O(MNK), making use of recent advances in random low-rank matrix approximation algorithms (Rokhlin et al. 2009). fastpca avoids computing the GRM and associated computational and memory storage costs, enabling PCA of very large datasets on standard hardware. We estimated the top 10 PCs of the WTCCC dataset (16k samples, 101k variants) in roughly 7 minutes while consuming 1GB of RAM, compared to 1 hour and 2.5GB for PLINK2. The fastpca approximation was extremely accurate (r2>99% between all fastpca and PLINK2 PCs). The improvement in running time becomes even larger at larger samples sizes; for example, fastpca estimated the top 10 PCs of a simulated data set with 100k samples and 300k variants in 135 minutes 8.5GB of RAM, vs. an estimated 350 hours and 85GB of RAM using PLINK2. A recently published O(MN2) time method, flashpca, did not complete on this data set due to exceeding 40GB memory requirement. All of these analyses were based on LD-pruning SNPs with r2>0.2, which leads to much more accurate PCs in simulations as compared to retaining all SNPs; more complex LD-adjustment strategies provide only a small further improvement.
Fast detection of IBD segments associated with quantitative traits in genome-wide association studies. Z. Wang, E. Kang, B. Han, S. Snir, E. Eskin.
   Recently, many methods have been developed to detect the identity-by-descent (IBD) segments between a pair of individuals. These methods are able to detect very small shared IBD segments between a pair of individuals up to 2 centimorgans in length. This IBD information can be used to identify recent rare mutations associated with phenotype of interest. Previous approaches for IBD association were applicable to case/control phenotypes. In this work, we propose a novel and natural statistic for the IBD association testing, which can be applied to quantitative traits. A drawback of the statistic is that it requires a large number of permutations to assess the significance of the association, which can be a great computational challenge. We make a connection between the proposed statistic and linear models so that it does not require permutations to assess the significance of an association. In addition, our method can control population structure by utilizing linear mixed models.
Long-range haplotype mapping in Hispanic/Latinos reveals loci for short stature. G. Belbin, D. Ruderfer, K. Slivinski, M.C. Yee, J. Jeff, O. Gottesman, E.A. Stahl, R.J.F. Loos, E.P. Bottinger, E.E. Kenny.
   The Hispanic/Latino (HL) population of Northern Manhattan represents a diverse recent diaspora population, with 95% of the individuals reporting having grandparents born outside of the United States. Of these 43% report grandparents born in Puerto Rico, 23% the Dominican Republic, 13% Central America, and 5%, 4%, and 2% from Mexico, South America, and Europe respectively. Despite complex patterns of migration, admixture, and diversity, strong signatures of cryptic relatedness persist amongst HLs. We have detected long-range genomic tract sharing (>3cM), or identity-by-descent (IBD), across 5,194 HL in the Mount Sinai BioMe Biobank. We observed an average population level IBD sharing of 0.0025 in HL, which is 2.5- and 5-fold higher than that observed in BioMe European- and African-American populations, respectively. We hypothesize that these patterns of recent migration and genetic drift may drive some otherwise rare functional alleles to detectable frequency. We clustered groups of homologous IBD tracts (n=112,250) segregating in this HL population. We observed that IBD clusters represent a class of low frequency alleles (median minor allele frequency =0.0077, s.d.=0.0015). We performed a genome-wide association of the IBD clusters, or ‘population-based linkage’, to detect loci implicated in height, a highly heritable polygenic trait. 15 independent loci surpassed our empirically derived genome-wide significance threshold of less than 4.4710-4, 11 of which replicated in an independent cohort of BioMe HLs. Strikingly, two regions confer strong recessive effects. In the case of the top hit on 9q32 (MAF less than 0.005; p less than8x10-6), homozygous non-referent individuals were shorter by 6” or 10”, for men or women, respectively, compared to the population mean (5’ 7” and 5’ 2” for men and women, respectively). In addition, IBD haplotypes in the 9q32 cluster harbored a significant enrichment of Native American ancestry (p less than 1x10-16). Finally, this interval contains a number of biologically compelling candidate genes, including COL27A1 and PALM2. This study demonstrates that rich population structure, rather than being a confounding factor in biomedical discovery efforts, may be leveraged to reveal novel genetic associations with complex human traits.
A haplotype reference panel of over 31,000 individuals and next-generation imputation methods. S. Das, on behalf of Haplotype Reference Consortium.
   Genotype imputation is now a key tool in the analysis of human genetic studies, enabling array-based genetic association studies to examine the millions of variants that are being discovered by advances in whole genome sequencing. Examining these variants increases power and resolution of genetic association studies and makes it easier to compare the results of studies conducted using different arrays. Genotype imputation improves in accuracy with increasing numbers of sequenced samples, particularly for low frequency variants. The goal of the Haplotype Reference Consortium is to combine haplotype information from ongoing whole genome sequencing studies to create a large imputation resource. To date, we have collected information on >31,500 sequenced whole genomes, aggregated over 20 studies of predominantly European ancestry, to create a very large reference panel of human haplotypes where ~50M genetic variants are observed 5 or more times. These haplotypes can be used to guide genotype imputation and haplotype estimation. In preliminary empirical evaluations, our panel provides substantial increases in accuracy relative to the 1000 Genomes Project Phase 1 reference panel and other smaller panels, particularly for variants with frequency less than 
5%. I will describe our evaluation of strategies for merging haplotypes and variant lists across studies and advances in methods for genotype likelihood-based haplotype estimation that can be applied to 10,000s of samples. I will also summarize new methods for next generation imputation that perform faster and require less memory than contemporary methods while attaining similar levels of imputation accuracy. Our full resource is available to the community through imputation servers that enable scientists to impute missing variants in any study and respect the privacy of subjects contributing to the studies that constitute the Haplotype Reference Consortium. The majority of haplotypes will also be deposited in the European Genotype Archive.
A rare variant local haplotype sharing method with application to admixed populations. S. Hooker, G. T. Wang, B. Li, Y. Guan, S. M. Leal.
   With the advent of next generation sequencing there is great interest in studying the involvement of rare variants in complex trait etiology. For many complex traits sequence data is being generated on DNA samples from African Americans and Hispanics to elucidate rare variant associations. Analyses of admixed populations present special challenges due to spurious associations which can occur because of confounding. However using information on admixture and local ancestry can also be highly beneficial and increase the power to detect associations in these populations. Here a local haplotype sharing (LHS) method (Xu and Guan 2014) was extended to test for rare variant (RV) associations in admixed populations. Previously the Weighted Haplotype and Imputation-based Test (WHAIT) (Li et al. 2010) was proposed to test for rare variant associations using haplotype data. The RV-LHS method unlike WHAIT, does not require reconstruction of haplotypes which can be both computationally intensive and error prone. Additionally the RV-LHS uses information on local ancestry which is particularly advantageous when analyzing admixed populations. Results will be shown from simulation studies performed for rare variant data from an admixed population. Both Type I and II errors are evaluated for the RV-LHS method. Additionally the power of the RV-LHS method is compared to WHAIT as well as several other non-haplotype-based rare variant association methods including the combined multivariate collapsing (CMC) (Li and Leal, 2008), Variable Threshold (VT) (Price et al. 2010) and Sequence Kernel Association Test (SKAT) (Wu et al. 2010). Several heart, lung and blood phenotypes were analyzed using sequence data on African-Americans from the NHLBI-Exome Sequencing Project to better evaluate the performance of the RV-LHS compared to other rare variant association methods.


batman said...

Accentuates the old theory that the human origin is a hybrid of an ape and an X.

Question to be dignified: What specie may constitute the missing link?

Grey said...

One thing on Sardinia is people in the interior mountainous region apparently have one of the highest proportiosn of centenarians in the world and the men live as long as the women.

apostateimpressions said...

> We find in particular that while the Anglo-Saxon samples resemble more closely the modern British population than the earlier samples, the Iron Age samples share more low frequency variation than the later ones with present day samples from southern Europe, in particular Spain (1000GP IBS). In addition the Anglo-Saxon period samples appear to share a stronger older component with Finnish (1000GP FIN) individuals. <

I take it that they are saying that the modern British are closer to the Anglo-Saxons than to the Iron Age British. Hopefully the study will quantify their estimate of Germanic input in Britain.

That would be consistent with the earlier study that found that England is 80-100% Germanic depending on the region, judging by the frequency of the "Frisian" Y segment. Scotland (lol) and Wales are mainly Germanic and northern Ireland is about 50%.

Is the present study suggesting that the Iron Age British were closer to modern Spain than to modern Ireland?"

The abstract seems a bit "cagey".

apostateimpressions said...

> In addition the Anglo-Saxon period samples appear to share a stronger older component with Finnish (1000GP FIN) individuals. <

That component presumably attests to contact in Scandinavia between the Germanic ancestors and Finns, possibly during the period when the Nordic Bronze culture extended to the coasts of Finland, some time after 3500 ybp.

Slumbery said...


I do not exactly understand what are you talking about. Your wording suggest you think of an admixture from a considerably different non-human group.
The article "Statistical inference of archaic introgression and natural selection in Central African Pygmies" is about the long assumed archaic human admixture in Africa that happened mostly after expansion of modern humans, therefore did not contribute in the Eurasian gene pool, so hardly have anything to do with "human origin".
Also a source is one or more archaic human population similar to the contemporary Neanderthals. They were apes, but only in the sense as Neanderthals and modern humans are, so this is not a meaningful classification in this case.
And they do not have a name yet, they are generally called "archaic Africans", because - due to the disadvantageous climate - the remains are scarce compared to Neanderthals. That is why the introgression has to be inferred the from the analysis of current genomes, we do not have archaic DNA from the region.

Unknown said...


Is the present study suggesting that the Iron Age British were closer to modern Spain than to modern Ireland?

The Irish are absent from the 1000 Genomes sample set, which I presume this study is limited to. Given that there's practically no genetic difference between any two regions of the British Isles, I'd be surprised if any post-Neolithic inhabitants of the Isles have been significantly different from one another. Otherwise, population replacement would have to have been ultimately near-ubiquitous (or at least regionally comparable), whether in one sweep, or from several similar sources in various regions.

The difference between the Iron Age Britons and the Anglo Saxons may be larger than that between modern Cornish (i.e. the most Brythonic modern English) and the Kentish (i.e. among the most Germanic English) samples -- which is minimal anyway -- though the abstract states that all these ancient samples fall consistently within the N. European range of variation. It suggests the greatest differences were found in rare variation in the two sample populations, which may well prove insignificant in the context of the wider genome.

That component presumably attests to contact in Scandinavia between the Germanic ancestors and Finns

Finns are the only other N. European population in the 1000 Genomes data set (other than CEU, who are basically Britons anyway), so Finns are just a proxy -- probably simply for the fact that Anglo Saxons had a slightly higher Hunter gatherer-to-farmer ratio than the Iron Age populations, and/or that at least an element of the HG component in Anglo Saxons was more similar to that in continental N. Europeans than was the HG component of Iron Age samples (whose HG ancestry was probably more indigenous). Likewise, the farmer element -- or at least part of it -- in Iron Age Britons was likely more similar to the farmer component in Iberians than could be said about the farmer component in Anglo Saxons. My take.

Simon_W said...

The idea that Wales and Scotland are predominantly Germanic is quite outlandish. If they were, why did they speak Celtic tongues until quite recently? If the Anglo-Saxon invaders had been in the majority there, they wouldn't have given up their language for fun and started to speak like the minority. (Afaik southeastern Scotland was Anglo-Saxon, though.)

apostateimpressions said...

I am pretty open minded about the deeper ancestry of the modern British, rightly so as I am just an interested casual amateur.

The modern British are all closer to Scandinavian hunter-gatherers than to western European h-gs? The French and Spanish are closer to western h-gs than to Scandinavian h-gs?

I begin to suspect that the modern British descend from waves of migration tracable to Scandinavia. That seems to be true of the Germanic migrations, which are tracable back to the Nordic Bronze Age? Maybe it is tracable back to the west of the Corded Ware? That might explain the levels of Ancient North Eurasian ancestry in the British, if the expansion of ANE into western Europe is linked with Corded Ware?

The close affinity of English and Scots and their nearness to Scandinavian h-gs seems to suggest that is true also of Scots: they descend from waves of Scandinavians.

Thus I suspect that it simply is not true that the modern British descend from h-gs who are "local" also to the modern French and Spanish.

I suspect that we need to think a little more afield when we speak of the British as "indigenous"; the island perhaps encourages an insular interpretation of "indigenous" to the British whereas it is better understood as "local" in the sense of Germany (yea I know, that one wont go down well.)

Perhaps someone more learned could indicate whether studies have provided information that might confirm or refute any of this?

"The idea that Wales and Scotland are predominantly Germanic is quite outlandish."

Maybe you are right Simon, but the genetic closeness of all of the British Isles that Hamar Fox alluded to, does suggest, given the accepted Anglo-Saxon invasions, that "population replacement would have to have been ultimately near-ubiquitous"?

apostateimpressions said...

I will critique my own early morning comment.

Yes the British do sit closer to Scandinavian H-gs than to Western European h-gs, but is that because of ANEA admixture in Scandinavian h-gs? One can draw a line between WHGS and ANE and Scandinavian HGs, and the British, sit along the line.

Also note, "France" clusters with the Scandinavians and the British while "southern France" and Spain do not.

Also, interesting to read that Scotland is 10% more HG + ANEA than the English. (I could have told them that just from my eyes.) I got that titbit from a newspaper and I would have had to pay bucks to read the actual study apart from the leading paragraph. ANEA is anyway closely related to WHG. (I speculated a couple of years back about a HG "continuum" across western NEA from looking at Odin iconography.)

Oh well, I least I admit my limitations. But I do think that there is a PC conspiracy to hide the truth from the British about themselves. After all, we are "all immigrants now and F the past." The English are German LOL even though the British establishment hates the Germans above all.

Come on Oxbridge, QUANTIFY Germanic input in Britain. At this late stage silence will be interpreted as an admission of guilt, of deceiving a people so that you can destroy them.

Slumbery said...

"The idea that Wales and Scotland are predominantly Germanic is quite outlandish."

Maybe you are right Simon, but the genetic closeness of all of the British Isles that Hamar Fox alluded to, does suggest, given the accepted Anglo-Saxon invasions, that "population replacement would have to have been ultimately near-ubiquitous"?

While Scotland and Wales were never mentioned in this context, but the idea that the pre-Anglo-Saxon population of Britain/England was already partially Germanic is not new. Some Historians suggested that the Roman sources were mistaken about the ethnic identity of the tribes that moved from present day Belgium to Britain at their time.

And for Wales and Scotland: until today their genes had two full millennia to spread and it is not like Wales and Scotland are that much isolated, not to mention the Scandinavian impact is Scotland later.

Simon_W said...

Apostateimpressions, I think the expansion of ANE in Europe was most of all caused by the West Asian expansion, which was, presumably, the PIE expansion. Only partly, to a smaller degree, the ANE expansion was caused by eastern hunter-gatherers as well. I'm thinking that R1b-M269 went from southeastern European hunter-gatherers to the local Neolithic and Chalcolithic cultures and expanded further from there, together with some ANE admixture from the hunter-gatherers. R1a was perhaps from eastern European hunter-gatherers, or, as has been recently suggested, from Western Asia. In any case the R1a expansion increased the ANE admixture as well. As did the J2 expansion.

Yes, in that PCA plot you linked to, the French and Spanish are closer to Scandinavian hunter-gatherers, as well. Only the Basques are roughly equidistant to Scandinavian and western hunter-gatherers. This has nothing to do with a Scandinavian expansion, but with the ubiquitous ANE admixture that differentiates modern Europeans from western hunter-gatherers and makes them closer to the Scandinavian ones.

BTW, the Nordic Bronze Age wasn't limited to Scandinavia, it was also present in Denmark and northern Germany.

There definitely was some Scandinavian immigration to Britain long before the Viking Age (as attested by the recent isotope analyses Chad Rohlfsen mentioned, also by some archeological and cranial evidence mentioned by Coon), but that this impact was strong seems unlikely.

The ubiquitous presence of that Frisian type y-chromosome may be pre-Germanic. After all the Frisians are neither Angles nor Saxons, and it's unknown when they became Germanic speaking.

This new study presented on the ASHG conference will hopefully answer our questions about the Anglo-Saxon impact.

Unknown said...


Maybe you are right Simon, but the genetic closeness of all of the British Isles that Hamar Fox alluded to, does suggest, given the accepted Anglo-Saxon invasions, that "population replacement would have to have been ultimately near-ubiquitous"?

There are four possibilities I can think of for why all British Islanders are so similar:

1) Both indigenous and invading populations were genetically near-identical

2) Every modern region of the British Isles is essentially the same ratio of indigenous population and Germanic invader (though the Germanic source would obviously vary by the region of Britain in question)

3) Invaders made little impact on the British gene pool

4) Invaders almost completely replaced the indigenous population

I've always strongly favoured scenario 1). There's barely any genetic difference even between the Irish and the Dutch, and in what little differences do exist between them, the English fairly consistently occupy an intermediate position. This is true both with PCAs and ADMIXTURE values.

Scenario 2) seems a little unlikely, at least if we want it to explain how it could mask the admixture of two deeply different populations. The only thing going for the idea that different Germanic/continental sources that currently differ from Britons can be compatible with the fact of modern British Isles internal genetic coherence, IMO, is that we actually see something of the sort with Orcadians. Genetically, they appear as a typical British Isles population and don't stand out much as a British-Norwegian admix, which I can only explain by assuming the Norwegian population has changed since its settlement of Orkney -- presumably by admixture with deeply different, East-Asian admixed Saami and Finns. Some Norwegians cluster near Britons in the same way Dutch, Germans and Danes do, presumably because these individual Norwegians have less of the mentioned admixture.

The abstract here seems to rule out scenario 3), and seems to support scenario 4) over my own preferred scenario 1). We really need to see the paper, though. We don't know how much closer the AS sample is to modern Britons than the IA sample. If they don't break down the 1000 Genomes GBR sample by region, then the collective sample is going to be about 1/3 Cornish, 1/3 Kentish, and 1/3 Orcadian (with a handful from Argyll). That makes 2/3 of the GBR sample 'heavily Germanic', probably above the British average, which may explain the stronger affinity. If they also find that Cornish, Welsh, even Irish are closer to the AS sample than they are to the IA sample, that would be quite a finding.

Simon_W said...

I've just had a „heureka“-experience. The famous West Asian component is in reality a compound of old population layers + the Gedrosia component. That this is true can be seen in the ADMIXTURE analysis in Lazaridis et al. 2013. And it also explains the two Iron Age Bulgarians: One had a very strong Caucasus component, but only little West Asian, and no Gedrosia. The other had a very strong West Asian component, a very strong Gedrosia component, and a weaker Caucasus component. Therefore we can conclude that the West Asian component came into being with the arrival of the Gedrosia component.

Modern populations from the Caucasus have all a strong Gedrosia-derived influence and are hence strongly West Asian. Some ancient farmers like Ötzi have still enough similarity with modern Caucasus populations to have a strong Caucasus component, even though they nearly lack the West Asian component. With the arrival of Gedrosia in SE Europe, this became to a large degree absorbed into the Caucasus component that was already there. That explains why SE Europeans are less Gedrosia than NW Europeans in Dodecad K12b, even though they are more West Asian.

In my opinion it's quite obvious that the Gedrosia component came together with R1b from the Iranian plateau. It moved westwards through western Asia and then went to SE Europe. It's partly responsible for the spread of ANE admixture. But ANE admixture in western Eurasia has two different peaks: One in the Caucasus, in Lezgins, a population rich in R1b. Quite a different peak are the Russians and Mordovians, populations rich in R1a. Thus it's very likely that R1a populations originated north of the Caucasus and that they too were responsible for the spread of ANE admixture.

ANE admixture didn't stay restricted to R1a and R1b people, they were just the Western Eurasians who had it first and most strongly. But I2 people in Scandinavia received some ANE admixture at quite an early date, and undeniably, J2 people also absorbed a lot of ANE.

I think this pattern suggests that the Proto-IEs were associated with R1b and that they originated in Western Asia. From there the language spread to R1a people north of the Caucasus who spread the language further. The areas where J2 is particularly strong are associated with non-IE languages like Lemnian-Pelasgian, the language of Linear A, Eteocretan, Eteocypriot, North Picene and Hattic.

Unknown said...

Having seen the preliminary results at Eurogenes, it seems I was correct in saying this:

"It suggests the greatest differences were found in rare variation in the two sample populations, which may well prove insignificant in the context of the wider genome."

The Iron Age Briton is dissimilar to Iberians, and not particularly dissimilar to modern Britons, though more Irish and Western Scottish-like than English-like or Cornish (and presumably Welsh)-like.

I'd say my scenario 1) pretty much holds up. It's likely that Norse, English, Welsh, Norman input into the Irish population, in addition to drift, make the IA sample an outlier -- albeit not much of one. Welsh-like and Saxon/Danish/Norman seem to count against affinity with the IA Celt, though Orcadians and Icelanders do plot close to him (possibly through the strength of similarity of their Celtic halves?). That there were better, currently unsampled ancestors of the Welsh and Cornish living in Iron Age Britain seems likely to me, unless significant Germanic population replacement occurred there, which, IMO, physical anthropology does not support. We will soon see anyway, if the AS sample is significantly closer to the Kentish than the Cornish sample.

So it seems to me that two of the three major ancestors to explain modern British variation have been discovered: Irish-like IA Celts, and English-like Anglo-Saxons (probably representative of all continental NW European input). IA samples from the west, particularly the darkest regions, may supply the third. All three groups were typically NW European, though probably a little more southerly in the case of the Welsh/Cornish ancestral population, so the impact of any on the average will be minuscule, and all regions likely have a proportion of each in them to varying degrees. Whether populations like the Picts represent a fourth population or fall into one of the two hypothesised IA populations we'll probably have to wait to find out.

Simon_W said...

Slumbery, I was replying to apostateimpressions' comment, he had brought Scotland and Wales into play. Indeed there were Belgae in southern Britain. The Belgae reportedly claimed to be of Germanic descent, but their personal and tribal names look Celtic, not Germanic. No matter what their language exactly was like, they presumably had more recent roots east of the Rhine than other western Europeans, which conveivably may have had some impact on their genetic make-up. Anyway, the upcoming paper will show what the pre-Roman population of southeastern Britain was like (the Catuvellauni in this case), how similar it was to present-day central Europeans and what the Anglo-Saxon influence has changed.

Simon_W said...

The preliminary results are very interesting, thanks for the hint, Hamar. What I find noteworthy: This Briton was found in Hinxton, in southern Cambridgeshire. Hence he probably belonged to the Catuvellauni. Who belonged to the Belgic tribes of Britain. Yet he is very northwestern European in the PCA, he's at the western extreme of the Irish, Orcadian, Western Scottish, Icelandic and Norwegian variation. There is no tendency at all towards continental Europe, Belgium, France, central Europe, Germany. Not even towards Kent. Therefore the Belgic impact in southeastern Britain doesn't appear to have pulled the local Celts a lot towards continental Europe. Perhaps it was more appreciable in the southeasternmost coastal tribes, but the Catuvellauni were Belgic too.

Simon_W said...

Important correction: It seems there has been a lot of confusion about which of the samples were Iron Age and which ones Anglo-Saxon. From what I've read on other blogs, it now seems that this individual, Hinxton No. 1 , is one of the three Anglo-Saxons. This is a fascinating finding, too. It shows that the Anglo-Saxons were strongly NW European and not dissimilar to Scots, Irish, Orcadians etc.

Simon_W said...

Correction of the correction: I've read that according to the latest information, Hinxton 1 and 4 must be the Iron Age samples, since reportedly all the Anglo-Saxon ones were female. But judging from Polako's analyses Hinxton 1, 2 and 3 are closest to Orcadians, Hinxton 4 to the Irish. The impression I get is one of much similarity between the British Celts and the Anglo-Saxons.