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

CNVassoc: Association analysis of CNV data using R.

BMC medical genomics - 24 May 2011

Subirana Isaac, Diaz-Uriarte Ramon, Lucas Gavin, Gonzalez Juan R

Abstract excerpt

BACKGROUND: Copy number variants (CNV) are a potentially important component of the genetic contribution to risk of common complex diseases. Analysis of the association between CNVs and disease requires that uncertainty in CNV copy-number calls, which can be substantial, be taken into account; failure to consider this uncertainty can lead to biased results. Therefore, there is a need to develop and use...

Read the complete abstract on PubMed

Topics

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

Share to Computational Biology
Share to Computer Simulation
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Models, Genetic

Share to Phenotype

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 21609482
DOI: 10.1186/1755-8794-4-47
PMCID: PMC3121578

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

CNVassoc: Association analysis of CNV data using R.PMID 21609482Read ↗

Accounting for uncertainty when assessing association between copy number and disease: a latent class model.Semantic proximity Read ↗

CNV-Profile Regression: A New Approach for Copy Number Variant Association Analysis in Whole Genome Sequencing DataSemantic proximity Read ↗

A robust statistical method for case-control association testing with copy number variation.Semantic proximity Read ↗

CONAN: copy number variation analysis software for genome-wide association studies.Semantic proximity Read ↗

CNV-seq, a new method to detect copy number variation using high-throughput sequencing.Semantic proximity Read ↗

A machine-learning approach for accurate detection of copy-number variants from exome sequencingSemantic proximity Read ↗

Modeling genetic inheritance of copy number variations.Semantic proximity Read ↗

A comparison of tools for copy-number variation detection in germline whole exome and whole genome sequencing dataSemantic proximity Read ↗

CNVPipe: An enhanced pipeline for accurate analysis of copy number variation from whole-genome sequencingSemantic proximity Read ↗

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

Targeted interrogation of copy number variation using SCIMMkit.Semantic proximity Read ↗

CNVoyant: A Highly Performant and Explainable Multi-Classifier Machine Learning Approach for Determining the Clinical Significance of Copy Number VariantsSemantic proximity Read ↗

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