Evidence map›Paper›PMID 40460117›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Study design and the sampling of deleterious rare variants in biobank-scale datasets.

Margaret C Steiner, Daniel P Rice, Arjun Biddanda, Mariadaria K Ianni-Ravn, Christian Porras, John Novembre

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. A sibling study of variation in parental mutation rates.bioRxiv : the preprint server for biology · 2026
    Article
  4. The distribution of highly deleterious variants across human ancestry groups.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Margaret C Steiner *Department of Human Genetics, University of Chicago, Chicago, IL 60637.ORCID 0000-0002-1062-1228
Daniel P Rice *Media Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-9509-2694
Arjun BiddandaDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218.ORCID 0000-0003-1861-1523
Mariadaria K Ianni-RavnDepartment of Human Genetics, University of Chicago, Chicago, IL 60637.ORCID 0000-0002-1814-9562
Christian PorrasDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, New York, NY 10029.
John NovembreDepartment of Human Genetics, University of Chicago, Chicago, IL 60637.

Funding

Theory, Methods, and Resources for Understanding and Leveraging Spatial Variation in Population Genetic DataR35GM149521 · NIGMS · UNIVERSITY OF CHICAGO · PI John Novembre · 2023 to 2026
$1.7M
Refining mutation rates and measures of purifying selection with an application to understanding the impact of non-coding variation on neuropsychiatric diseasesR01HG010773 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, XIN, NOVEMBRE, JOHN · 2020 to 2023
$1.7M
Extending Tools for Visualization of Geographic Structure in Population Genomic DataR01GM132383 · NIGMS · UNIVERSITY OF CHICAGO · PI NOVEMBRE, JOHN · 2019 to 2022
$1.4M
National Science Foundation (NSF) DGE1746045NHGRI NIH HHS R01 HG010773NIGMS NIH HHS R01 GM132383NIGMS NIH HHS R35 GM149521
6 · The paper itself

Abstract

One key component of study design in population genetics is the "geographic breadth" of a sample (i.e., how broad a region across which individuals are sampled). How the geographic breadth of a sample impacts observations of rare, deleterious variants is unclear, even though such variants are of particular interest for biomedical and evolutionary applications. Here, in order to gain insight into the effects of sample design on ascertained genetic variants, we formulate a stochastic model of dispersal, genetic drift, selection, mutation, and geographically concentrated sampling. We use this model to understand the effects of the geographic breadth of sampling effort on the discovery of negatively selected variants. We find that samples which are more geographically broad will discover a greater number of variants as compared to geographically narrow samples (an effect we label "discovery"); though the variants will be detected at lower average frequency than in narrow samples (e.g., as singletons, an effect we label "dilution"). Importantly, these effects are amplified for larger sample sizes and fitness effects. We validate these results using both population genetic simulations and empirical analyses in the UK Biobank. Our results are particularly important in two contexts: the association of large-effect rare variants with particular phenotypes and the inference of negative selection from allele frequency data. Overall, our findings emphasize the importance of considering geographic breadth when designing and carrying out genetic studies, especially at biobank scale.

Indexed as

Biological Specimen BanksGenetics, PopulationGenetic VariationResearch DesignGenetic DriftHumansModels, GeneticSelection, GeneticUnited Kingdomnegative selectionpopulation geneticsrare variants

Identifiers

PMID40460117
PMCPMC12167998

What OpenQuestion holds

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Registered trials

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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.