MetaCNV - a consensus approach to infer accurate copy numbers from low coverage data.

Stefanie FriedrichRemus BarbulescuThomas HelledayErik L L Sonnhammer

Published in: BMC medical genomics (2020)

MetaCNV, available at https://bitbucket.org/sonnhammergroup/metacnv, provides accurate copy number prediction on low coverage data and performs well on high coverage data.

Keyphrases

copy number
electronic health record
mitochondrial dna
big data
affordable care act
high resolution
dna methylation
gene expression
data analysis
mass spectrometry