A web-based tool for copy number variation (CNV) - based association studies. CoNVaQ has two models: 1. Fisher's exact test and 2. A novel query-based model matching regions to user-defined queries.
Pathology; DNA structural variation; Genetic variation; Genotype and phenotype
Larsen SJ, do Canto LM, Rogatto SR, Baumbach J "CoNVaQ: a web tool for copy number variation-based association studies." BMC Genomics. 2018 May 18;19(1):369. https://doi.org/10.1186/s12864-018-4732-8
PMID: 29776329
PMCID: PMC5960125
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