CNVrd, a Read-Depth Algorithm for Assigning Copy-Number at the FCGR Locus: Population-Specific Tagging of Copy Number Variation at FCGR3B
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
CNVrd, a Read-Depth Algorithm for Assigning Copy-Number at the FCGR Locus: Population-Specific Tagging of Copy Number Variation at FCGR3B
Authors
Keywords
-
Journal
PLoS One
Volume 8, Issue 4, Pages e63219
Publisher
Public Library of Science (PLoS)
Online
2013-05-02
DOI
10.1371/journal.pone.0063219
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Evidence that deletion at FCGR3B is a risk factor for systemic sclerosis
- (2012) C McKinney et al. GENES AND IMMUNITY
- Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes
- (2012) Cushla McKinney et al. HUMAN MOLECULAR GENETICS
- Confirmation of association ofFCGR3Bbut notFCGR3Acopy number with susceptibility to autoantibody positive rheumatoid arthritis
- (2012) James I. Robinson et al. HUMAN MUTATION
- cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate
- (2012) Günter Klambauer et al. NUCLEIC ACIDS RESEARCH
- Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms
- (2011) Catarina D. Campbell et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Tabix: fast retrieval of sequence features from generic TAB-delimited files
- (2011) H. Li BIOINFORMATICS
- The variant call format and VCFtools
- (2011) P. Danecek et al. BIOINFORMATICS
- Accuracy in Copy Number Calling by qPCR and PRT: A Matter of DNA
- (2011) Nora Fernandez-Jimenez et al. PLoS One
- Editorial: β-Defensins and Crohn's Disease: Confusion From Counting Copies
- (2010) Edward J Hollox AMERICAN JOURNAL OF GASTROENTEROLOGY
- Association of variation in Fc receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
- (2010) C. McKinney et al. ANNALS OF THE RHEUMATIC DISEASES
- Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease
- (2010) R. Colobran et al. CLINICAL AND EXPERIMENTAL IMMUNOLOGY
- Copy number, linkage disequilibrium and disease association in the FCGR locus
- (2010) H. A. Niederer et al. HUMAN MOLECULAR GENETICS
- Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity
- (2010) Sebastian M. Waszak et al. PLoS Computational Biology
- Association of Higher DEFB4 Genomic Copy Number With Crohn's Disease
- (2009) Robert W Bentley et al. AMERICAN JOURNAL OF GASTROENTEROLOGY
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
- (2009) M Mamtani et al. GENES AND IMMUNITY
- Sensitive and accurate detection of copy number variants using read depth of coverage
- (2009) S. Yoon et al. GENOME RESEARCH
- An integrated approach for measuring copy number variation at theFCGR3(CD16) locus
- (2009) Edward J. Hollox et al. HUMAN MUTATION
- Copy number variation at theFCGRlocus includesFCGR3A, FCGR2CandFCGR3Bbut notFCGR2AandFCGR2B
- (2009) Willemijn B. Breunis et al. HUMAN MUTATION
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- Personalized copy number and segmental duplication maps using next-generation sequencing
- (2009) Can Alkan et al. NATURE GENETICS
- Experimental aspects of copy number variant assays at CCL3L1
- (2009) Sarah F Field et al. NATURE MEDICINE
- Copy-number variants in neurodevelopmental disorders: promises and challenges
- (2009) Alison K. Merikangas et al. TRENDS IN GENETICS
- Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays
- (2008) Holly N. Cukier et al. ANALYTICAL BIOCHEMISTRY
- Integrated detection and population-genetic analysis of SNPs and copy number variation
- (2008) Steven A McCarroll et al. NATURE GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started