CoNVaQ: a web tool for copy number variation-based association studies.

Simon Jonas LarsenLuisa Matos do CantoSilvia Regina RogattoJan Baumbach

Published in: BMC genomics (2018)

CoNVaQ provides a simple workflow for performing CNV-based association studies. It is made available as a web platform in order to provide a user-friendly workflow for biologists and clinicians to carry out CNV data analysis without installing any software. Through the web interface, users are also able to analyze their results to find overrepresented GO terms and pathways. In addition, our method is also available as a package for the R programming language. CoNVaQ is available at https://convaq.compbio.sdu.dk .

Keyphrases

data analysis
copy number
mitochondrial dna
genome wide
electronic health record
palliative care
dna methylation
autism spectrum disorder
high throughput
gene expression