Unsupported: Use of this version of inferCNV is not supported. More information on our Applications Support and Retention Policy.InferCNV is used to explore tumor single cell RNA-Seq data to identify evidence for somatic large-scale chromosomal copy number alterations, such as gains or deletions of entire chromosomes or large segments of chromosomes.
Accessing inferCNV 1.12.0-foss-2021b-R-4.2.0
To load the module for inferCNV 1.12.0-foss-2021b-R-4.2.0 please use this command on the BEAR systems (BlueBEAR, BEARCloud VMs, and CaStLeS VMs):
module load bear-apps-unsupported/handbuilt/2019
module load inferCNV/1.12.0-foss-2021b-R-4.2.0
BEAR Apps Version
- infercnv 1.12.0
- parallelDist 0.2.6
For more information visit the inferCNV website.
Last modified on 21st July 2022