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Shuangning Li

Publications and source records attributed to Shuangning Li.

21 records · Page 2Linked to original sources

Average Direct and Indirect Causal Effects under Interference

We propose a definition for the average indirect effect of a binary treatment in the potential outcomes model for causal inference under cross-unit interference. Our definition is analogous to the standard definition of the average direct effect, and can be expressed without needing to compare outcomes across multiple randomized experiments. We show that the proposed indirect effect satisfies a decomposition theorem whereby, in a Bernoulli trial, the sum of the average direct and indirect effects always corresponds to the effect of a policy intervention that infinitesimally increases treatment probabilities. We also consider a number of parametric models for interference, and find that our non-parametric indirect effect remains a natural estimand when re-expressed in the context of these models.

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Transfer learning in genome-wide association studies with knockoffs

This paper presents and compares alternative transfer learning methods that can increase the power of conditional testing via knockoffs by leveraging prior information in external data sets collected from different populations or measuring related outcomes. The relevance of this methodology is explored in particular within the context of genome-wide association studies, where it can be helpful to address the pressing need for principled ways to suitably account for, and efficiently learn from the genetic variation associated to diverse ancestries. Finally, we apply these methods to analyze several phenotypes in the UK Biobank data set, demonstrating that transfer learning helps knockoffs discover more numerous associations in the data collected from minority populations, potentially opening the way to the development of more accurate polygenic risk scores.

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Searching for consistent associations with a multi-environment knockoff filter

This paper develops a method based on model-X knockoffs to find conditional associations that are consistent across diverse environments, controlling the false discovery rate. The motivation for this problem is that large data sets may contain numerous associations that are statistically significant and yet misleading, as they are induced by confounders or sampling imperfections. However, associations consistently replicated under different conditions may be more interesting. In fact, consistency sometimes provably leads to valid causal inferences even if conditional associations do not. While the proposed method is flexible and can be deployed in a wide range of applications, this paper highlights its relevance to genome-wide association studies, in which consistency across populations with diverse ancestries mitigates confounding due to unmeasured variants. The effectiveness of this approach is demonstrated by simulations and applications to the UK Biobank data.

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