Comparison of Multiple Methods for Determination of FCGR3A/B Genomic Copy Numbers in HapMap Asian Populations with Two Public Databases
Author:
Publisher
Frontiers Media SA
Subject
Genetics(clinical),Genetics,Molecular Medicine
Reference17 articles.
1. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans;Aitman;Nature,2006
2. Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura;Breunis;Blood,2008
3. Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B;Breunis;Hum. Mutat.,2009
4. Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients;Chen;Arthrit. Rheumatol.,2014
5. FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity;Fanciulli;Nat. Genet.,2007
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1. GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads;Scientific Reports;2023-10-18
2. Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios;Statistical Applications in Genetics and Molecular Biology;2018-04-25
3. AMYCNE: Confident copy number assessment using whole genome sequencing data;PLOS ONE;2018-03-26
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