Evidence map›Paper›PMID 41873523›Full record

ArticleGenome biology and evolution2026

Identifying Adaptive Footprints in the Presence of Demographic Uncertainty.

Sandipan Paul Arnab, Mohammad Khan, Andre Luiz Campelo Dos Santos, Matteo Fumagalli, Michael DeGiorgio

Abstract read
In one paragraph

Article in Genome biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Sandipan Paul ArnabDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL, USA.ORCID 0000-0003-0827-5327
Mohammad KhanDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL, USA.ORCID 0009-0007-6066-5409
Andre Luiz Campelo Dos SantosDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL, USA.ORCID 0000-0002-5577-1967
Matteo FumagalliSchool of Biological and Behavioural Sciences, Queen Mary University of London, London, UK.ORCID 0000-0002-4084-2953
Michael DeGiorgioDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL, USA.ORCID 0000-0003-4908-7234

Funding

Identifying complex modes of adaptation from population-genomic dataR35GM128590 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Michael DeGiorgio · 2018 to 2026
$2.8M
National Science Foundation DBI-2130666National Science Foundation DEB-1949268Natural Environment Research Council NE/Y003519/1NIGMS NIH HHS R35 GM128590NIH HHS R35GM128590
6 · The paper itself

Abstract

Identifying genomic regions shaped by natural selection is a central goal in evolutionary genomics. Existing machine learning methods for this task are typically trained on labeled data simulated according to specific evolutionary scenarios. While effective in controlled settings, these models are limited by their reliance on explicit class labels, detecting only the processes they were trained to recognize. This limitation makes it difficult to interpret predictions for regions shaped by other evolutionary forces, a problem especially acute when analyzing genomes influenced by mixtures of adaptive and demographic factors. One-vs-rest strategies offer a potential alternative but suffer from the complexity of modeling processes as a catch-all "rest" class. Here, we explore positive-unlabeled learning as a flexible framework for detecting adaptive events. This semi-supervised approach permits identification of a target class using only positive labels and an unlabeled background, without requiring explicit modeling of negatives. To assess its utility, we focus on a binary classification setting for detecting selective sweeps against a mixed background of unlabeled sweeps and neutrally evolving regions. We introduce PULSe, a method that trains only on labeled sweep observations while treating remaining data as unlabeled. By avoiding assumptions about background composition, PULSe enables robust sweep discovery in realistic genomic landscapes. We evaluate performance across demographic, adaptive, and confounding contexts, including domain shift from misspecified models, and find that PULSe delivers strong generalizability. Finally, analyzing European and Bengali genomes, we recapitulate known sweep candidates, demonstrating PULSe as a versatile tool for detecting adaptive regions across diverse genomic landscapes.

Indexed as

GenomicsModels, GeneticSelection, GeneticEvolution, MolecularHumansMachine LearningUncertaintyBengali in Bangladeshmachine learningmodel misspecificationnatural selectionpositive-unlabeled learning

Identifiers

PMID41873523
PMCPMC13049369

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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.