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Journal of the Royal Statistical Society Series B (Statistical Methodology)BioinformaticsPeer-reviewed journal article

A simple new approach to variable selection in regression, with application to genetic fine-mapping

Gao T. WangiD, Abhishek SarkariD, Peter S. CarbonettoiD, Matthew StephensiD

PDFDOIPreprint

Abstract summary

Claude Opus 5.5 · max effort · 17 Oct 2026 · from the abstract

SuSiE writes sparse regression coefficients as a sum of single-effect vectors; its IBSS algorithm returns a credible set per effect and outperformed existing fine-mapping methods in numerical experiments.

Genetic fine-mapping needs variable selection that reports how uncertain the choice of variable is, because predictors are highly correlated and detectable effects are sparse. Unlike traditional stepwise selection, which commits to one variable per step, the proposed IBSS procedure keeps stepwise simplicity but returns a distribution over variables and a credible set for each selection.

Key results

  1. ShownIBSS, a Bayesian analogue of stepwise selection, computes a distribution over variables at each step instead of picking one, and is formally shown to optimize a variational approximation to the SuSiE posterior, which yields a credible set of variables for each selected effect.

    Formal justification reported in the abstract; IBSS is said to share the simplicity and speed of traditional stepwise methods, but no runtimes are given. · Abstract

  2. SuggestedSuSiE fitted with IBSS outperformed existing methods for genetic fine-mapping, a setting the authors characterize by highly correlated variables and sparse detectable effects.

    Numerical experiments only; the abstract names no competing methods or performance metrics. · Abstract

  3. SuggestedThe methods were applied to fine-map genetic variants that influence alternative splicing in human cell lines.

    Presented as an illustration; the abstract reports no numbers of loci, variants or credible sets. · Abstract

Methods, data and reproducibility

The Sum of Single Effects (SuSiE) model expresses the sparse coefficient vector of a linear regression as a sum of single-effect vectors that each have exactly one non-zero entry; it is fitted by Iterative Bayesian Stepwise Selection (IBSS), justified as optimizing a variational approximation to the posterior, and evaluated in numerical experiments and a splicing fine-mapping example.

  • Numerical experiments comparing fine-mapping methods
  • Genetic variants influencing alternative splicing in human cell lines · human
Methods & tools
SuSiE, IBSS
Reproducibility gaps
The abstract gives no software link, implementation details or data source for the splicing application.
Limitations (3)
  • The authors note challenges, alongside potential, in applying these methods to generic variable selection problems beyond fine-mapping-like settings. · stated by the authors
  • The performance advantage rests on numerical experiments alone, and the abstract names neither the competing methods nor the metrics used. · noted in this summary
  • The splicing fine-mapping in human cell lines is only an illustration, with no reported loci, credible-set sizes or validation. · noted in this summary

Read this if you fine-map genetic associations or select variables among highly correlated predictors and want credible sets that quantify which variables to select.

Citations
1,120
FWCI
66.27
Field percentile
top 1%

Abstract

We introduce a simple new approach to variable selection in linear regression, with a particular focus on quantifying uncertainty in which variables should be selected. The approach is based on a new model -- the "Sum of Single Effects" (SuSiE) model -- which comes from writing the sparse vector of regression coefficients as a sum of "single-effect" vectors, each with one non-zero element. We also introduce a corresponding new fitting procedure -- Iterative Bayesian Stepwise Selection (IBSS) -- which is a Bayesian analogue of stepwise selection methods. IBSS shares the computational simplicity and speed of traditional stepwise methods, but instead of selecting a single variable at each step, IBSS computes a distribution on variables that captures uncertainty in which variable to select. We provide a formal justification of this intuitive algorithm by showing that it optimizes a variational approximation to the posterior distribution under the SuSiE model. Further, this approximate posterior distribution naturally yields convenient novel summaries of uncertainty in variable selection, providing a Credible Set of variables for each selection. Our methods are particularly well-suited to settings where variables are highly correlated and detectable effects are sparse, both of which are characteristics of genetic fine-mapping applications. We demonstrate through numerical experiments that our methods outper-form existing methods for this task, and illustrate their application to fine-mapping genetic variants influencing alternative splicing in human cell-lines. We also discuss the potential and challenges for applying these methods to generic variable selection problems.

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