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

CNV discovery using SNP genotyping arrays.

Cytogenetic and genome research - 1 Jan 2008

Yau C, Holmes C C

Abstract excerpt

Genome-wide single nucleotide polymorphism (SNP) genotyping platforms have made an important contribution to population genetics and genetic epidemiology. Recently there has been a realisation that these SNP platforms can also be used for typing copy number variants (CNVs). This allows for 'generalised' genotyping of both SNPs and CNVs simultaneously on a common sample set, with advantages in terms of cost and...

Read the complete abstract on PubMed

Topics

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

Share to Gene Dosage
Share to Models, Genetic
Share to Oligonucleotide Array Sequence Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 19287169
DOI: 10.1159/000184722

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

CNV discovery using SNP genotyping arrays.PMID 19287169Read ↗

Detection of copy number variation using SNP genotyping.Semantic proximity Read ↗

Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.Semantic proximity Read ↗

Identification of Copy Number Variants from SNP Arrays Using PennCNV.Semantic proximity Read ↗

A systematic benchmark of copy number variation detection tools for high density SNP genotyping arrays.Semantic proximity Read ↗

Comparing CNV detection methods for SNP arrays.Semantic proximity Read ↗

Rare copy number variant analysis in case-control studies using snp array data: a scalable and automated data analysis pipeline.Semantic proximity Read ↗

Systematic assessment of copy number variant detection via genome-wide SNP genotyping.Semantic proximity Read ↗

Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.Semantic proximity Read ↗

Rare Copy Number Variant analysis in case-control studies using SNP Array Data: a scalable and automated data analysis pipelineSemantic proximity Read ↗

Accurate and Effective Detection of Recurrent Copy Number Variants in Large SNP Genotype Datasets.Semantic proximity Read ↗

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.Semantic proximity Read ↗

Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances.Semantic proximity Read ↗

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