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

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

Cytogenetic and genome research - 1 Jan 2006

Zhang J, Feuk L, Duggan G E, Khaja R, Scherer S W

Abstract excerpt

The discovery of an abundance of copy number variants (CNVs; gains and losses of DNA sequences >1 kb) and other structural variants in the human genome is influencing the way research and diagnostic analyses are being designed and interpreted. As such, comprehensive databases with the most releva...

Read the complete abstract on PubMed

Topics

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

Share to Data Interpretation, Statistical
Share to Databases, Genetic
Share to Genetic Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Internet

Share to Nucleic Acid Hybridization

Share to Programming Languages

Share to Statistics as Topic

Share to User-Computer Interface

Source

Identifiers

PMID: 17124402
DOI: 10.1159/000095916

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-17124402-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.PMID 17124402Read ↗

Strategies for the detection of copy number and other structural variants in the human genome.Semantic proximity Read ↗

Interactive analysis of large cancer copy number studies with Copy Number Explorer.Semantic proximity Read ↗

Accurate and reliable high-throughput detection of copy number variation in the human genome.Semantic proximity Read ↗

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.Semantic proximity Read ↗

Detecting copy number variation in the human genome using comparative genomic hybridization.Semantic proximity Read ↗

Comparative genomic hybridization.Semantic proximity Read ↗

CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Semantic proximity Read ↗

Finding common regions of alteration in copy number data.Semantic proximity Read ↗

Copy number estimation algorithms and fluorescence in situ hybridization to describe copy number alterations in human tumors.Semantic proximity Read ↗

Copy-number-variation and copy-number-alteration region detection by cumulative plots.Semantic proximity Read ↗

A Guide to Using ClinTAD for Interpretation of DNA Copy Number Variants in the Context of Topologically Associated Domains.Semantic proximity Read ↗

Use of Affymetrix Arrays in the Diagnosis of Gene Copy-Number Variation.Semantic proximity Read ↗

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