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

Copy-number polymorphisms: mining the tip of an iceberg.

Trends in genetics : TIG - 1 Jun 2005

Buckley Patrick G, Mantripragada Kiran K, Piotrowski Arkadiusz, Diaz de Ståhl Teresita, Dumanski Jan P

Abstract excerpt

Copy-number polymorphisms (CNPs) represent a greatly underestimated aspect of human genetic variation. Recently, two landmark studies reported genome-wide analyses of CNPs in normal individuals and represent the beginning of an understanding of this type of large-scale variation. Future array-CGH-based CNP analyses should include standard criteria on a common microarray platform. It is only when parallel analyses...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 22
Share to CNP gene
Share to Gene Dosage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 15922827
DOI: 10.1016/j.tig.2005.04.007

Genes

CNP

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

Copy-number polymorphisms: mining the tip of an iceberg.PMID 15922827Read ↗

Population-genetic properties of differentiated human copy-number polymorphisms.Semantic proximity Read ↗

Copy-number variation and association studies of human disease.Semantic proximity Read ↗

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Semantic proximity Read ↗

Germline copy number polymorphisms involving larger than 100 kb are uncommon in normal subjects.Semantic proximity Read ↗

Array-based DNA diagnostics: let the revolution begin.Semantic proximity Read ↗

Genomic copy number variation, human health, and disease.Semantic proximity Read ↗

Large-scale copy number polymorphism in the human genome.Semantic proximity Read ↗

Gene copy number variation and common human disease.Semantic proximity Read ↗

Copy-number variations add a new layer of complexity in the human genome.Semantic proximity Read ↗

A copy number variation map of the human genome.Semantic proximity Read ↗

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

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.Semantic proximity Read ↗

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