Evidence map›Paper›PMID 39230693›Full record

ArticleBioinformatics (Oxford, England)2024

Scalable CNN-based classification of selective sweeps using derived allele frequencies.

Sjoerd van den Belt, Hanqing Zhao, Nikolaos Alachiotis

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sjoerd van den BeltDepartment of Computer Science, Faculty of EEMCS, University of Twente, 7522NB Enschede, The Netherlands.
Hanqing ZhaoDepartment of Computer Science, Faculty of EEMCS, University of Twente, 7522NB Enschede, The Netherlands.
Nikolaos AlachiotisDepartment of Computer Science, Faculty of EEMCS, University of Twente, 7522NB Enschede, The Netherlands.ORCID 0000-0001-8162-3792

Funding

Dutch Research CouncilNWO KICH1.ST04.22.033
6 · The paper itself

Abstract

motivationSelective sweeps can successfully be distinguished from neutral genetic data using summary statistics and likelihood-based methods that analyze single nucleotide polymorphisms (SNPs). However, these methods are sensitive to confounding factors, such as severe population bottlenecks and old migration. By virtue of machine learning, and specifically convolutional neural networks (CNNs), new accurate classification models that are robust to confounding factors have been recently proposed. However, such methods are more computationally expensive than summary-statistic-based ones, yielding them impractical for processing large-scale genomic data. Moreover, SNP data are frequently preprocessed to improve classification accuracy, further exacerbating the long analysis times.

resultsTo this end, we propose a 1D CNN-based model, dubbed FAST-NN, that does not require any preprocessing while using only derived allele frequencies instead of summary statistics or raw SNP data, thereby yielding a sample-size-invariant, scalable solution. We evaluated several data fusion approaches to account for the variance of the density of genetic diversity across genomic regions (a selective sweep signature), and performed an extensive neural architecture search based on a state-of-the-art reference network architecture (SweepNet). The resulting model, FAST-NN, outperforms the reference architecture by up to 12% inference accuracy over all challenging evolutionary scenarios with confounding factors that were evaluated. Moreover, FAST-NN is between 30× and 259× faster on a single CPU core, and between 2.0× and 6.2× faster on a GPU, when processing sample sizes between 128 and 1000 samples. Our work paves the way for the practical use of CNNs in large-scale selective sweep detection. AVAILABILITY AND IMPLEMENTATION: https://github.com/SjoerdvandenBelt/FAST-NN.

Indexed as

Gene FrequencyNeural Networks, ComputerPolymorphism, Single NucleotideAlgorithmsHumansMachine LearningSelection, Genetic

Identifiers

PMID39230693
PMCPMC11373383

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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.