Abstract
AbstractCausal discovery is a powerful tool to disclose underlying structures by analyzing purely observational data. Genetic variants can provide useful complementary information for structure learning. Here, we propose a novel algorithm MRSL (Mendelian Randomization (MR)-based Structure Learning algorithm), which combines the graph theory with univariable and multivariable MR to learn the true structure using only GWAS summary statistics. Specifically, MRSL also utilizes topological sorting to improve the precision of structure learning and provides three adjusting categories for multivariable MR. Results of simulation reveal that MRSL has up to two-fold higher F1 score than other eight competitive methods. Additionally, the computing time of MRSL is 100 times faster than other methods. Furthermore, we apply MRSL to 26 biomarkers and 44 ICD10-defined diseases from UK Biobank. The results cover most of expected causal links which have biological interpretations and several new links supported by clinical case reports or previous observational literatures.
Publisher
Cold Spring Harbor Laboratory
Reference77 articles.
1. Pearl, J. Causality: Models, Reasoning and Inference (Cambridge University Press, 2009).
2. Spirtes, P. , Glymour, C. & Scheines, R. Causation, Prediction, and Search 2nd edn, Vol. 1 (The MIT Press, 2001).
3. Pathway Commons at Virtual Cell: use of pathway data for mathematical modeling
4. Using Bayesian Networks to Analyze Expression Data
5. A system for automated general medical diagnosis using Bayesian networks;MedInfo,2013
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献