broadinstitute/inferCNV: Infer Copy Number Variation from Single-Cell RNA-Seq Data
Using single-cell RNA-Seq expression to visualize CNV in cells.
Getting started
Browse package contents
Package details |
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| Bioconductor views | Bayesian CopyNumberVariation Genetics GenomicVariation HiddenMarkovModel SingleCell Software StatisticalMethod StructuralVariation Transcriptomics VariantDetection |
| Maintainer | |
| License | BSD_3_clause + file LICENSE |
| Version | 1.19.1 |
| URL | https://github.com/broadinstitute/inferCNV/wiki |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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