infercnv-package: infercnv: Infer Copy Number Variation from Single-Cell...
In broadinstitute/infercnv: Infer Copy Number Variation from Single-Cell RNA-Seq Data
infercnv-package R Documentation
infercnv: Infer Copy Number Variation from Single-Cell RNA-Seq Data
Description
Using single-cell RNA-Seq expression to visualize CNV in cells.
Details
The main functions you will need to use are CreateInfercnvObject() and run(infercnv_object).
For additional details on running the analysis step by step, please refer to the example vignette.
Author(s)
Maintainer: Christophe Georgescu cgeorges@broadinstitute.org
Authors:
Timothy Tickle ttickle@broadinstitute.org
Itay Tirosh tirosh@broadinstitute.org
Maxwell Brown mbrown@broadinstitute.org
Brian Haas bhaas@broadinstitute.org
See Also
Useful links:
broadinstitute/infercnv documentation built on April 26, 2024, 4:11 a.m.
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| infercnv-package | R Documentation |
infercnv: Infer Copy Number Variation from Single-Cell RNA-Seq Data
Description
Using single-cell RNA-Seq expression to visualize CNV in cells.
Details
The main functions you will need to use are CreateInfercnvObject() and run(infercnv_object). For additional details on running the analysis step by step, please refer to the example vignette.
Author(s)
Maintainer: Christophe Georgescu cgeorges@broadinstitute.org
Authors:
Timothy Tickle ttickle@broadinstitute.org
Itay Tirosh tirosh@broadinstitute.org
Maxwell Brown mbrown@broadinstitute.org
Brian Haas bhaas@broadinstitute.org
See Also
Useful links:
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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