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Barbara A Thomson

Publications and source records attributed to Barbara A Thomson.

2 recordsLinked to original sources

Population structure inferred by local spatial autocorrelation: an example from an Amerindian tribal population.

Spatial autocorrelation (SA) methods were recently extended to detect local spatial autocorrelation (LSA) at individual localities. LSA statistics serve as useful indicators of local genetic population structure. We applied this method to 15 allele frequencies from 43 villages of a South American tribe, the Yanomama. Based on a network of links <or=51 km between neighboring villages, we calculated LSA statistics for Moran, Geary, and Getis-Ord coefficients. We also developed two new, rescaled indices of local SA. Local indicators of positive SA highlight villages surrounded by genetically similar near neighbors. Negative LSA statistics indicate sharp genetic differences from near neighbors. Markedly positive LSA was found for all 11 outlier villages. The most negatively LSA villages are in the central, densely connected cluster. The Getis-Ord coefficients of suitably transformed allele frequencies point to clusters of villages with unusually high or low allelic polymorphisms. The most homozygous villages are all in the four geographically isolated village clusters. The most polymorphic villages are all in the large, densely settled Yanomame dialect group. An ad hoc linguistic isolation index between neighboring villages showed that villages in isolated pairs and triplets have linguistically similar neighbors, whereas nine villages with notably negative LSA are all near dialect and kinship boundaries. The location of a village with respect to the graph structure of its neighborhood affects its LSA and genetic polymorphism. The implications of these findings for the population structure of the Yanomama are compatible with those from an earlier study of global SA in these villages.

Demography↗

A new protocol for evaluating putative causes for multiple variables in a spatial setting, illustrated by its application to European cancer rates.

We introduce a statistical protocol for analyzing spatially varying data, including putative explanatory variables. The procedures comprise preliminary spatial autocorrelation analysis (from an earlier study), path analysis, clustering of the resulting set of path diagrams, ordination of these diagrams, and confirmatory tests against extrinsic information. To illustrate the application of these methods, we present incidence and mortality rates of 31 organ- and sex-specific cancers in Europe; these rates vary markedly with geography and type of cancer. Additionally, we investigated three factors (ethnohistory, genetics, and geography) putatively affecting these rates. The five variables were correlated separately for the 31 cancers over European reporting stations. We analyzed the correlations by path analysis, k-means clustering, and nonmetric multidimensional scaling; coefficients of the 31 path diagrams modeling the correlations vary substantially. To simplify interpretation, we grouped the diagrams into five clusters, for which we describe the differential effects of the three putative causes on incidence and mortality. When scaled, the path coefficients intergrade without marked gaps between clusters. Ethnic differences make for differences in cancer rates, even when the populations tested are ancient and complex mixtures. Path analysis usefully decomposes a structural model involving effects and putative causes, and estimates the magnitude of the model's components. Smooth intergradation of the path coefficients suggests the putative causes are the results of multiple forces. Despite this continuity of the path diagrams of the 31 cancers, clustering offers a useful segmentation of the continuum. Etiological and other extrinsic information on the cancers map significantly into the five clusters, demonstrating their epidemiological relevance.

Biometry↗