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Paula Gablenz

Publications and source records attributed to Paula Gablenz.

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Searching for local associations while controlling the false discovery rate

We introduce local conditional hypotheses that express how the relation between explanatory variables and outcomes changes across different contexts, described by covariates. By expanding upon the model-X knockoff filter, we show how to adaptively discover these local associations, all while controlling the false discovery rate. Our enhanced inferences can help explain sample heterogeneity and uncover interactions, making better use of the capabilities offered by modern machine learning models. Specifically, our method is able to leverage any model for the identification of data-driven hypotheses pertaining to different contexts. Then, it rigorously test these hypotheses without succumbing to selection bias. Importantly, our approach is efficient and does not require sample splitting. We demonstrate the effectiveness of our method through numerical experiments and by studying the genetic architecture of Waist-Hip-Ratio across different sexes in the UKBiobank.

stat.ME

Catch me if you can: Signal localization with knockoff e-values

We consider problems where many, somewhat redundant, hypotheses are tested and we are interested in reporting the most precise rejections, with false discovery rate (FDR) control. This is the case, for example, when researchers are interested both in individual hypotheses as well as group hypotheses corresponding to intersections of sets of the original hypotheses, at several resolution levels. A concrete application is in genome-wide association studies, where, depending on the signal strengths, it might be possible to resolve the influence of individual genetic variants on a phenotype with greater or lower precision. To adapt to the unknown signal strength, analyses are conducted at multiple resolutions and researchers are most interested in the more precise discoveries. Assuring FDR control on the reported findings with these adaptive searches is, however, often impossible. To design a multiple comparison procedure that allows for an adaptive choice of resolution with FDR control, we leverage e-values and linear programming. We adapt this approach to problems where knockoffs and group knockoffs have been successfully applied to test conditional independence hypotheses. We demonstrate its efficacy by analyzing data from the UK Biobank.

stat.ME