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Veliz-Otani, D.

Publications and source records attributed to Veliz-Otani, D..

3 recordsLinked to original sources

Unifying population structure and relatedness analysis through a coalescent approach

Standard methods in genome-wide association studies (GWAS) partition genetic similarity into recent familial relationship, modeled by a genetic relationship matrix (GRM), and distant relatedness, adjusted for using principal components (PCs). This practice relies on an implicit causal model that conflates population structure with confounding. Here, we challenge this approach by developing a unified framework grounded in coalescent theory. We introduce the Coefficient of Genealogical Similarity (GeSi), a statistic derived from a model of shared derived alleles that captures the full continuum of shared ancestry and can be estimated directly from genotype data. This leads to a new classification of GRMs into "full" matrices, which capture the complete genealogy, and "shallow" matrices, which measure only recent relatedness. Systematic benchmarking demonstrates that full GRMs are sufficient to model the genetic covariance from population structure, rendering PC adjustment for this purpose redundant. This finding clarifies that the justifiable role for PCs in such a model is to correct for true environmental or complex genetic confounders. Our analyses of empirical data confirm that including PCs can improve model fit, providing evidence that such confounding is present and correlated with axes of genetic variation. This work establishes a new theoretical framework that disentangles the modeling of genealogical relatedness from the correction of confounding, reframing the role of PCs as proxies for the latter and challenging the rationale for including the top PCs merely to capture maximal genetic variance.

genetics↗

Peruvian Population Genomics: Unraveling the Genetic Landscape and Admixture Dynamics of Urban Populations

Latin American populations exhibit high genetic and phenotypic diversity shaped by complex admixture histories, yet remain underrepresented in genomic research. Here, we analyze genome-wide data from 432 urban individuals across 13 regions of Peru, including 346 newly genotyped from the Peruvian Genome Project. We revealed fine-scale population structure and demographic patterns shaped by both ancient and recent events. Indigenous American ancestries in urban individuals trace back to ancient north-south interactions consisted with archaeological records, while admixture events occurring within the last 8-10 generations involved sources already admixed between distinct ancestral lineages. Identity-by-descent analyses reveal sustained gene flow in southern Peru, while effective population size trends highlight demographic stability in Lima over the past 25 generations. Sex-biased admixture patterns suggest Indigenous ancestry contribution preferentially mediated by females. These findings offer a comprehensive view of Perus genetic heritage, advancing our understanding of human genetic diversity and historical demographic processes in Latin America.

genetics↗

Genetics of Latin American Diversity (GLAD) Project: insights into population genetics and association studies in recently admixed groups in the Americas

Latin America is underrepresented in genetic studies, which can exacerbate disparities in personalized genomic medicine. However, genetic data of thousands of Latin Americans are already publicly available, but require a bureaucratic maze to navigate all the data access and consenting issues. We present the Genetics of Latin American Diversity (GLAD) Project, a platform that compiles genome-wide information of 54,077 Latin Americans from 39 studies representing 45 geographical regions. Through GLAD, we identified heterogeneous ancestry composition and recent gene-flow across the Americas. Also, we developed a simulated-annealing-based algorithm to match the genetic background of external samples to our database and share summary statistics without transferring individual-level data. Finally, we demonstrate the potential of GLAD as a critical resource for evaluating statistical genetic softwares in the presence of admixture. By making this resource available, we promote genomic research in Latin Americans and contribute to the promises of personalized medicine to more people.

genetics↗