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

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays.

Nucleic acids research - 1 May 2010

Dellinger Andrew E, Saw Seang-Mei, Goh Liang K, Seielstad Mark, Young Terri L, Li Yi-Ju

Abstract excerpt

Determination of copy number variants (CNVs) inferred in genome wide single nucleotide polymorphism arrays has shown increasing utility in genetic variant disease associations. Several CNV detection methods are available, but differences in CNV call thresholds and characteristics exist. We evalua...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Computer Simulation
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomic variations and chromosomal abnormalities

Share to Myopia

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

Share to Prenatal Screening and Diagnostics

Source

Open in PubMed Open full text

Identifiers

PMID: 20142258
DOI: 10.1093/nar/gkq040
PMCID: PMC2875020

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20142258-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays.PMID 20142258Read ↗

Current analysis platforms and methods for detecting copy number variation.Semantic proximity Read ↗

Application of Nexus copy number software for CNV detection and analysis.Semantic proximity Read ↗

Copy Number Variation.Semantic proximity Read ↗

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

Progress in Methods for Copy Number Variation Profiling.Semantic proximity Read ↗

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.Semantic proximity Read ↗

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.Semantic proximity Read ↗

An integrative segmentation method for detecting germline copy number variations in SNP arrays.Semantic proximity Read ↗

The effect of algorithms on copy number variant detection.Semantic proximity Read ↗

Joint estimation of DNA copy number from multiple platforms.Semantic proximity Read ↗

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

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

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