Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Testing neutrality at copy-number-variable loci under the finite-allele and finite-site models.

Theoretical population biology - 1 Dec 2016

Hu Xin-Sheng, Hu Yang, Chen Xiaoyang

Abstract excerpt

Copy-number variation (CNV) is an important form of DNA structural variation because a certain proportion of genomes in many eukaryotic species can contribute to such variations. Owing to the differences between CNVs and single nucleotide polymorphisms (SNPs) in size, mutation rate and maintaining mechanism, it is more realistic to characterize CNV evolution under the finite-allele and finite-site models. Here,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to DNA Copy Number Variations
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genome, Human

Share to Genotype

Share to Mutation

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 27423854
DOI: 10.1016/j.tpb.2016.07.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Testing neutrality at copy-number-variable loci under the finite-allele and finite-site models.PMID 27423854Read ↗

Exploring the role of copy number variants in human adaptation.Semantic proximity Read ↗

Analysis of Population-Genetic Properties of Copy Number Variations.Semantic proximity Read ↗

Gene copy-number polymorphism in nature.Semantic proximity Read ↗

On a novel coalescent model for genome-wide evolution of copy number variations.Semantic proximity Read ↗

Population-genetic nature of copy number variations in the human genome.Semantic proximity Read ↗

Quantitative analysis of single nucleotide polymorphisms within copy number variation.Semantic proximity Read ↗

Empirical Validation of the Nearly Neutral Theory at Divergence and Population-Genomic Scales Using 144 Placental Mammal Genomes.Semantic proximity Read ↗

A practical case-control association test for detecting a susceptibility allele at a copy number variation locus.Semantic proximity Read ↗

Demography-adjusted tests of neutrality based on genome-wide SNP data.Semantic proximity Read ↗

Reduced purifying selection prevails over positive selection in human copy number variant evolution.Semantic proximity Read ↗

Thermal adaptation rather than demographic history drives genetic structure inferred by copy number variants in a marine fish.Semantic proximity Read ↗

Detecting Selection on Segregating Gene Duplicates in a Population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.