Causal Discovery and Optimal Experimental Design for Genome-Scale Biological Network Recovery
원문 초록
Causal discovery of genome-scale networks is important for identifying pathways from genes to observable traits - e.g. differences in cell function, disease, drug resistance and others. Causal learners based on graphical models rely on interventional samples to orient edges in the network. However, these models have not been shown to scale up the size of the genome, which are on the order of 1e3-1e4 genes. We introduce a new learner, SP-GIES, that jointly learns from interventional and observational datasets and achieves almost 4x speedup against an existing learner for 1,000 node networks. SP-GIES achieves an AUC-PR score of 0.91 on 1,000 node networks, and scales up to 2,000 node networks - this is 4x larger than existing works. We also show how SP-GIES improves downstream optimal experimental design strategies for selecting interventional experiments to perform on the system. This is an important step forward in realizing causal discovery at scale via autonomous experimental design.
함께 살펴볼 논문
공통 태그를 근거로 연결했습니다. 실제 인용 관계나 논문의 우수성을 뜻하지 않습니다.
Can Large Language Models Help Experimental Design for Causal Discovery?
Paths to Causality: Finding Informative Subgraphs Within Knowledge Graphs for Knowledge-Based Causal Discovery
ALINE: Joint Amortization for Bayesian Inference and Active Data Acquisition
Permutation-Free High-Order Interaction Tests
Assessing parameter identifiability of a hemodynamics PDE model using spectral surrogates and dimension reduction
TimeGraph: Synthetic Benchmark Datasets for Robust Time-Series Causal Discovery
토론
이 논문과 연결된 포럼 글이 아직 없습니다.