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MR-Clust: clustering of genetic variants in Mendelian randomization with similar causal estimates
Author(s) -
Christopher N. Foley,
Amy M. Mason,
Paul Kirk,
Stephen Burgess
Publication year - 2020
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btaa778
Subject(s) - mendelian randomization , spurious relationship , cluster analysis , causal inference , cluster (spacecraft) , computer science , computational biology , biology , statistics , genetic variants , genetics , gene , artificial intelligence , machine learning , mathematics , genotype , programming language
Mendelian randomization is an epidemiological technique that uses genetic variants as instrumental variables to estimate the causal effect of a risk factor on an outcome. We consider a scenario in which causal estimates based on each variant in turn differ more strongly than expected by chance alone, but the variants can be divided into distinct clusters, such that all variants in the cluster have similar causal estimates. This scenario is likely to occur when there are several distinct causal mechanisms by which a risk factor influences an outcome with different magnitudes of causal effect. We have developed an algorithm MR-Clust that finds such clusters of variants, and so can identify variants that reflect distinct causal mechanisms. Two features of our clustering algorithm are that it accounts for differential uncertainty in the causal estimates, and it includes 'null' and 'junk' clusters, to provide protection against the detection of spurious clusters.

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