SG-ADVISER CNV: copy-number variant annotation and interpretation.

Galina A EriksonNeha DeshpandeBalachandar G KesavanAli Torkamani

Published in: Genetics in medicine : official journal of the American College of Medical Genetics (2014)

Scripps Genome ADVISER CNV is designed to allow users with no prior bioinformatics expertise to manipulate large volumes of copy-number variant data. Scripps Genome ADVISER CNV is available at http://genomics.scripps.edu/ADVISER/.

Keyphrases

copy number
genome wide
mitochondrial dna
dna methylation
single cell
rna seq
big data
gene expression
machine learning
deep learning