Proceedings of the National Academy of Sciences · 2021 · 92 citations · 46 references
Life SciencesGeneticsMolecular GeneticsGenomicsHuman GeneticsPopulation GeneticsGenome SequencingPopulation Genetics InferencePopulation GenomicsTurkey GeneticsGenetic AdmixtureGenetic Relationship AnalysisGenetic Relationship MatrixGenome-wide Admixture AnalysisInbreeding CoefficientsInherited Disease GeneticsPopulation Genetic StructureRare Disease Gene Discovery
= 773) were sequenced to generate a Turkish (TR) Variome that should serve to facilitate disease gene discovery in Turkey. Consistent with the history of present-day Turkey as a crossroads between Europe and Asia, we found extensive admixture between Balkan, Caucasus, Middle Eastern, and European populations with a closer genetic relationship of the TR population to Europeans than hitherto appreciated. We determined that 50% of TR individuals had high inbreeding coefficients (≥0.0156) with runs of homozygosity longer than 4 Mb being found exclusively in the TR population when compared to 1000 Genomes Project populations. We also found that 28% of exome and 49% of genome variants in the very rare range (allele frequency < 0.005) are unique to the modern TR population. We annotated these variants based on their functional consequences to establish a TR Variome containing alleles of potential medical relevance, a repository of homozygous loss-of-function variants and a TR reference panel for genotype imputation using high-quality haplotypes, to facilitate genome-wide association studies. In addition to providing information on the genetic structure of the modern TR population, these data provide an invaluable resource for future studies to identify variants that are associated with specific phenotypes as well as establishing the phenotypic consequences of mutations in specific genes.
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