Evidence map›Paper›PMID 39560456›Full record

ArticleGenetics2024

Bayesian hierarchical hypothesis testing in large-scale genome-wide association analysis.

Anirban Samaddar, Tapabrata Maiti, Gustavo de Los Campos

Abstract read
In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Genome-wide fine-mapping improves identification of causal variants.medRxiv : the preprint server for health sciences · 2025
    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.

Anirban SamaddarDepartment of Statistics and Probability, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-9520-8012
Tapabrata MaitiDepartment of Statistics and Probability, Michigan State University, East Lansing, MI 48824, USA.
Gustavo de Los CamposDepartment of Statistics and Probability, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-5692-7129

Funding

pleioR: A powerful and fast test and software for the study of pleiotropy in systems involving many traits with biobank-sized dataR03HG011674 · NHGRI · MICHIGAN STATE UNIVERSITY · PI DE LOS CAMPOS, GUSTAVO · 2021 to 2022
$157k
NHGRI NIH HHS R03 HG011674NIH HHS R03HG011674NSF DMS-1952856, PGRP-035472 and 1924724
6 · The paper itself

Abstract

Variable selection and large-scale hypothesis testing are techniques commonly used to analyze high-dimensional genomic data. Despite recent advances in theory and methodology, variable selection and inference with highly collinear features remain challenging. For instance, collinearity poses a great challenge in genome-wide association studies involving millions of variants, many of which may be in high linkage disequilibrium. In such settings, collinearity can significantly reduce the power of variable selection methods to identify individual variants associated with an outcome. To address such challenges, we developed a Bayesian hierarchical hypothesis testing (BHHT)-a novel multiresolution testing procedure that offers high power with adequate error control and fine-mapping resolution. We demonstrate through simulations that the proposed methodology has a power-FDR performance that is competitive with (and in many scenarios better than) state-of-the-art methods. Finally, we demonstrate the feasibility of using BHHT with large sample size (n∼ 300,000) and ultra dimensional genotypes (∼ 15 million single-nucleotide polymorphisms or SNPs) by applying it to eight complex traits using data from the UK-Biobank. Our results show that the proposed methodology leads to many more discoveries than those obtained using traditional SNP-centered inference procedures. The article is accompanied by open-source software that implements the methods described in this study using algorithms that scale to biobank-size ultra-high-dimensional data.

Indexed as

Bayesian hierarchical hypothesis testingBayesian variable selectioncollinearityfalse discovery rateGWASlinkage disequilibriummultiresolution inferencespike and slab priorUK-Biobank data

Identifiers

PMID39560456
PMCPMC11631447

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.