Normalizes data from multiple genetic screens, such as for example siRNA screens or CRISPR-Cas9 screens, possibly corresponding to different cell lines. Using an invariant set of values for each replicate, it quantile-normalizes all replicates while preserving differences in phenotype between them. Raw data can be read in as tab-delimited files, and must include gene and feature annotation, in particular indicating which features are part of the library and which ones are negative/positive controls.
Package details |
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Author | Renee Menezes [aut, cre] |
Maintainer | Renee Menezes <r.menezes@vumc.nl> |
License | GPL-3 |
Version | 1.0.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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