Stable Differentiable Causal DiscoveryAchille Nazaret, Justin Hong, Elham Azizi et al.
Inferring causal relationships as directed acyclic graphs (DAGs) is an important but challenging problem. Differentiable Causal Discovery (DCD) is a promising approach to this problem, framing the search as a continuous optimization. But existing DCD methods are numerically unstable, with poor performance beyond tens of variables. In this paper, we propose Stable Differentiable Causal Discovery (SDCD), a new method that improves previous DCD methods in two ways: (1) It employs an alternative constraint for acyclicity; this constraint is more stable, both theoretically and empirically, and fast to compute. (2) It uses a training procedure tailored for sparse causal graphs, which are common in real-world scenarios. We first derive SDCD and prove its stability and correctness. We then evaluate it with both observational and interventional data and on both small-scale and large-scale settings. We find that SDCD outperforms existing methods in both convergence speed and accuracy and can scale to thousands of variables. We provide code at https://github.com/azizilab/sdcd.
11.5LGAug 29, 2023
The CausalBench challenge: A machine learning contest for gene network inference from single-cell perturbation dataMathieu Chevalley, Jacob Sackett-Sanders, Yusuf Roohani et al.
In drug discovery, mapping interactions between genes within cellular systems is a crucial early step. Such maps are not only foundational for understanding the molecular mechanisms underlying disease biology but also pivotal for formulating hypotheses about potential targets for new medicines. Recognizing the need to elevate the construction of these gene-gene interaction networks, especially from large-scale, real-world datasets of perturbed single cells, the CausalBench Challenge was initiated. This challenge aimed to inspire the machine learning community to enhance state-of-the-art methods, emphasizing better utilization of expansive genetic perturbation data. Using the framework provided by the CausalBench benchmark, participants were tasked with refining the current methodologies or proposing new ones. This report provides an analysis and summary of the methods submitted during the challenge to give a partial image of the state of the art at the time of the challenge. Notably, the winning solutions significantly improved performance compared to previous baselines, establishing a new state of the art for this critical task in biology and medicine.
28.6LGJun 16, 2019
Robust Federated Learning in a Heterogeneous EnvironmentAvishek Ghosh, Justin Hong, Dong Yin et al.
We study a recently proposed large-scale distributed learning paradigm, namely Federated Learning, where the worker machines are end users' own devices. Statistical and computational challenges arise in Federated Learning particularly in the presence of heterogeneous data distribution (i.e., data points on different devices belong to different distributions signifying different clusters) and Byzantine machines (i.e., machines that may behave abnormally, or even exhibit arbitrary and potentially adversarial behavior). To address the aforementioned challenges, first we propose a general statistical model for this problem which takes both the cluster structure of the users and the Byzantine machines into account. Then, leveraging the statistical model, we solve the robust heterogeneous Federated Learning problem \emph{optimally}; in particular our algorithm matches the lower bound on the estimation error in dimension and the number of data points. Furthermore, as a by-product, we prove statistical guarantees for an outlier-robust clustering algorithm, which can be considered as the Lloyd algorithm with robust estimation. Finally, we show via synthetic as well as real data experiments that the estimation error obtained by our proposed algorithm is significantly better than the non-Byzantine-robust algorithms; in particular, we gain at least by 53\% and 33\% for synthetic and real data experiments, respectively, in typical settings.