broadinstitute/infercnvApp

This is an R shiny app created as a user friendly way to run the R package infercnv. 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. More information on infercnv can be found on the infercnv Github Page

语言：R · GitHub 星标：4 · Fork：4

在 GitHub 上查看原仓库