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

Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.

Genome biology - 22 Dec 2012

Cardoso-Moreira Margarida, Arguello J Roman, Clark Andrew G

Abstract excerpt

BACKGROUND: The detailed study of breakpoints associated with copy number variants (CNVs) can elucidate the mutational mechanisms that generate them and the comparison of breakpoints across species can highlight differences in genomic architecture that may lead to lineage-specific differences in patterns of CNVs. Here, we provide a detailed analysis of Drosophila CNV breakpoints and contrast it with similar...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Breakpoints
Share to DNA
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Drosophila melanogaster

Share to Genome, Insect

Share to Homologous Recombination

Share to Molecular Sequence Data

Source

Open in PubMed Open full text

Identifiers

PMID: 23259534
DOI: 10.1186/gb-2012-13-12-r119
PMCID: PMC4056370

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.PMID 23259534Read ↗

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.Semantic proximity Read ↗

Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing.Semantic proximity Read ↗

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterizationSemantic proximity Read ↗

DNA sequence features underlying large-scale duplications and deletions in humanSemantic proximity Read ↗

Complex human chromosomal and genomic rearrangements.Semantic proximity Read ↗

A method for complete characterization of complex germline rearrangements from long DNA readsSemantic proximity Read ↗

Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 familiesSemantic proximity Read ↗

Drosophila larval brain neoplasms present tumour-type dependent genome instabilitySemantic proximity Read ↗

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome.Semantic proximity Read ↗

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history.Semantic proximity Read ↗

Deciphering new insights into copy number variations as drivers of genomic diversity and adaptation in farm animal species.Semantic proximity Read ↗

Origins and breakpoint analyses of copy number variations: up close and personal.Semantic proximity Read ↗

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