Evidence map›Paper›PMID 35769876›Full record

ArticleiScience2022

Uncertainty quantification in variable selection for genetic fine-mapping using bayesian neural networks.

Wei Cheng, Sohini Ramachandran, Lorin Crawford

Abstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Wei ChengDepartment of Computer Science, Brown University, Providence, RI, USA.
Sohini RamachandranDepartment of Computer Science, Brown University, Providence, RI, USA.
Lorin CrawfordCenter for Computational Molecular Biology, Brown University, Providence, RI, USA.

Funding

Population-genetic methods for inferring recent histories and targets of selection in the biobank eraR35GM139628 · NIGMS · BROWN UNIVERSITY · PI Sohini Ramachandran · 2021 to 2026
$2.2M
Novel statistical methods to localize genomic elements underlying adaptive evolutionR01GM118652 · NIGMS · BROWN UNIVERSITY · PI RAMACHANDRAN, SOHINI · 2016 to 2020
$1.6M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NIGMS NIH HHS R01 GM118652NIGMS NIH HHS R35 GM139628Wellcome Trust
6 · The paper itself

Abstract

In this paper, we propose a new approach for variable selection using a collection of Bayesian neural networks with a focus on quantifying uncertainty over which variables are selected. Motivated by fine-mapping applications in statistical genetics, we refer to our framework as an "ensemble of single-effect neural networks" (ESNN) which generalizes the "sum of single effects" regression framework by both accounting for nonlinear structure in genotypic data (e.g., dominance effects) and having the capability to model discrete phenotypes (e.g., case-control studies). Through extensive simulations, we demonstrate our method's ability to produce calibrated posterior summaries such as credible sets and posterior inclusion probabilities, particularly for traits with genetic architectures that have significant proportions of non-additive variation driven by correlated variants. Lastly, we use real data to demonstrate that the ESNN framework improves upon the state of the art for identifying true effect variables underlying various complex traits.

Indexed as

Artificial intelligenceBioinformaticsGenetics

Identifiers

PMID35769876
PMCPMC9234235

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.