Evidence map›Paper›PMID 41928457›Full record

ArticleGenome biology and evolution2026

Detecting Positive Selection by Modeling Structure Within Images of Genetic Variation.

Md Ruhul Amin, Sandipan Paul Arnab, Mohammad Khan, 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. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Md Ruhul AminDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL 33431, USA.ORCID 0000-0002-4282-5153
Sandipan Paul ArnabDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL 33431, USA.ORCID 0000-0003-0827-5327
Mohammad KhanDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL 33431, USA.ORCID 0009-0007-6066-5409
Michael DeGiorgioDepartment of Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL 33431, 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 BCS-2001063National Science Foundation DBI-2130666National Science Foundation DEB-1949268NIGMS NIH HHS R35 GM128590NIH HHS R35GM128590
6 · The paper itself

Abstract

A major challenge in population genomics is accurately identifying and characterizing natural selection from genomic data. The wide availability of dense whole-genome datasets has enabled researchers to analyze and localize genetic variation within populations. Powerful supervised machine learning methods allow researchers to extract spatial information about genetic variation across the genome and identify traces of natural selection. While convolutional neural networks capture correlations among neighboring features, design choices such as heavy-pooling or limited receptive fields can lead to loss of fine-grained spatial resolution. Extensions like dilated convolutions or attention mechanisms mitigate this issue of loss of spatial resolution but at the cost of increased architectural complexity and parameter count when capturing correlations at different scales. In contrast, trend filtering directly models the autocovariation of neighboring features, ensuring that spatial relationships remain intact without any architectural extensions. When integrated into a classical machine learning model, such as a support vector machine, trend filtering offers a natural framework to create powerful predictive models while retaining the spatial integrity of the input. Here, we introduce SKINET, which employs a novel trend filter kernel within a support vector machine framework and apply it to the task of detecting and characterizing regions affected by positive natural selection. Specifically, SKINET not only distinguishes regions under positive natural selection from neutrally evolving regions but also functions in a regression framework to estimate associated adaptive parameters. Moreover, applying SKINET to empirical human genome variation identifies adaptive candidate genes consistent with previous findings while also uncovering novel adaptation targets, such as FAM177A1, that are linked to cancer.

Indexed as

Genetic VariationModels, GeneticSelection, GeneticHumansSupport Vector Machinehaplotype variationmachine learningselective sweepsupport vector machine

Identifiers

PMID41928457
PMCPMC13089544

What OpenQuestion holds

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LicenceCC BY-NC
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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.