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Ragsdale, A. P.

Publications and source records attributed to Ragsdale, A. P..

22 records · Page 2Linked to original sources

Unbiased estimation of linkage disequilibrium from unphased data

Linkage disequilibrium is used to infer evolutionary history and to identify regions under selection or associated with a given trait. In each case, we require accurate estimates of linkage disequilibrium from sequencing data. Unphased data presents a challenge because the co-occurrence of alleles at different loci is ambiguous. Commonly used estimators for the common statistics r2 and D2 exhibit large and variable upward biases that complicate interpretation and comparison across cohorts. Here, we show how to find unbiased estimators for a wide range of two-locus statistics, including D2, for both single and multiple randomly mating populations. These provide accurate estimates over three orders of magnitude in LD. We also use these estimators to construct an estimator for r2 that is less biased than commonly used estimators, but nevertheless argue for using [Formula] rather than r2 for population size estimates.

genetics↗

Models of archaic admixture and recent history from two-locus statistics

We learn about population history and underlying evolutionary biology through patterns of genetic polymorphism. Many approaches to reconstruct evolutionary histories focus on a limited number of informative statistics describing distributions of allele frequencies or patterns of linkage disequilibrium. We show that many commonly used statistics are part of a broad family of two-locus moments whose expectation can be computed jointly and rapidly under a wide range of scenarios, including complex multi-population demographies with continuous migration and admixture events. A full inspection of these statistics reveals that widely used models of human history fail to predict simple patterns of linkage disequilibrium. To jointly capture the information contained in classical and novel statistics, we implemented a tractable likelihood-based inference framework for demographic history. Using this approach, we show that human evolutionary models that include archaic admixture in Africa, Asia, and Europe provide a much better description of patterns of genetic diversity across the human genome. We estimate that an unidentified, deeply diverged population admixed with modern humans within Africa both before and after the split of African and Eurasian populations, contributing 4 - 8% genetic ancestry to individuals in world-wide populations.\n\nAuthor SummaryThroughout human history, populations have expanded and contracted, split and merged, and ex-changed migrants. Because these events affected genetic diversity, we can learn about human history by comparing predictions from evolutionary models to genetic data. Here, we show how to rapidly compute such predictions for a wide range of diversity measures within and across populations under complex demographic scenarios. While widely used models of human history accurately predict common measures of diversity, we show that they strongly underestimate the co-occurence of low frequency mutations within human populations in Asia, Europe, and Africa. Models allowing for archaic admixture, the relatively recent mixing of human populations with deeply diverged human lineages, resolve this discrepancy. We use such models to infer demographic models that include both recent and ancient features of human history. We recover the well-characterized admixture of Neanderthals in Eurasian populations, as well as admixture from an as-yet unknown diverged human population within Africa, further suggesting that admixture with deeply diverged lineages occurred multiple times in human history. By simultaneously testing model predictions for a broad range of diversity statistics, we can assess the robustness of common evolutionary models, identify missing historical events, and build more informed models of human demography.

genetics↗

Perspective: Genomic inference using diffusion models and the allele frequency spectrum

Evolutionary, biological, and demographic processes combine to shape the variation observed in populations. Understanding how these processes are expected to influence variation allows us to infer past demographic events and the nature of selection in human populations. Forward models such as the diffusion approximation provide a powerful tool for analyzing the distribution of allele frequencies in contemporary populations due to their computational tractability and model flexibility. Here, we discuss recent computational developments and their application to reconstructing human demographic history and patterns of selection at new mutations. We also reexamine how some classical assumptions that are still commonly used in inference studies fare when applied to modern data. We use whole-genome sequence data for 797 French Canadian individuals to examine the neutrality of synonymous sites. We find that selection can lead to strong biases in the inferred demography, mutation rate, and distributions of fitness effects. We use these distributions of fitness effects together with demographic and phenotype-fitness models to predict the relationship between effect size and allele frequency, and contrast those predictions to commonly used models in statistical genetics. Thus the simple evolutionary models investigated by Kimura and Ohta still provide important insight into modern genetic research.

genetics↗

Inferring demographic history using two-locus statistics

Population demographic history may be learned from contemporary genetic variation data. Methods based on aggregating the statistics of many single loci into an allele frequency spectrum (AFS) have proven powerful, but such methods ignore potentially informative patterns of linkage disequilibrium (LD) between neighboring loci. To leverage such patterns, we developed a composite-likelihood framework for inferring demographic history from aggregated statistics of pairs of loci. Using this framework, we show that two-locus statistics are indeed more sensitive to demographic history than single-locus statistics such as the AFS. In particular, two-locus statistics escape the notorious confounding of depth and duration of a bottleneck, and they provide a means to estimate effective population size based on the recombination rather than mutation rate. We applied our approach to a Zambian population of Drosophila melanogaster. Notably, using both single- and two-locus statistics, we found substantially lower estimates of effective population size than previous works. Together, our results demonstrate the broad potential for two-locus statistics to enable powerful population genetic inference.

genetics↗