Evidence map›Paper›PMID 40100752›Full record

ArticleGenome biology and evolution2025

Inferring the Selective History of CNVs Using a Maximum Likelihood Model.

Seyed Amir Malekpour, Ata Kalirad, Sina Majidian

Abstract read
In one paragraph

Article in Genome biology and evolution, 2025. 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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2 · The registry

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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

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5 · Who and what money

Authors and funding

3 authors.

Seyed Amir MalekpourSchool of Biological Sciences, Institute for Research in Fundamental Sciences (IPM), Tehran 19395-5746, Iran.ORCID 0000-0002-3525-3548
Ata KaliradDepartment for Integrative Evolutionary Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.ORCID 0000-0002-9500-3903
Sina MajidianSIB Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland.ORCID 0000-0001-5345-6982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copy number variations (CNVs)-structural variations generated by deletion and/or duplication that result in a change in DNA dosage-are prevalent in nature. CNVs can drastically affect the phenotype of an organism and have been shown to be both involved in genetic disorders and be used as raw material in adaptive evolution. Unlike single-nucleotide variations, the often large and varied effects of CNVs on phenotype hinders our ability to infer their selective advantage based on the population genetics data. Here, we present a likelihood-based approach, dubbed PoMoCNV (POlymorphism-aware phylogenetic MOdel for CNVs), that estimates the evolutionary parameters such as mutation rates among different copy numbers and relative fitness loss per copy deletion at a genomic locus based on population genetics data. As a case study, we analyze the genomics data of 40 strains of Caenorhabditis elegans, representing four different populations. We take advantage of the data on chromatin accessibility to interpret the mutation rate and fitness of copy numbers, as inferred by PoMoCNV, specifically in open or closed chromatin loci. We further test the reliability of PoMoCNV by estimating the evolutionary parameters of CNVs for mutation-accumulation experiments in C. elegans with varying levels of genetic drift.

Indexed as

Caenorhabditis elegansDNA Copy Number VariationsEvolution, MolecularModels, GeneticAnimalsLikelihood FunctionsMutation RatePhylogenySelection, GeneticC. eleganscopy number variationslikelihood-based inferencepolymorphism-aware phylogenetic model

Identifiers

PMID40100752
PMCPMC11950529

What Socratic 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 Socratic graph.