diff options
author | Ricardo Wurmus <rekado@elephly.net> | 2024-11-28 11:34:48 +0100 |
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committer | Ricardo Wurmus <rekado@elephly.net> | 2024-12-03 16:59:56 +0100 |
commit | e3bbf678e374a255bb0f97793c3a90fc799f53d0 (patch) | |
tree | 242203c10ebab3837302550e9ef0cfed9b3b8cd4 /gnu/packages/bioinformatics.scm | |
parent | dff6f586884a35d6531437f42f4425cb844634fa (diff) |
gnu: Remove r-numbat.
This is a duplicate of a package in (gnu packages bioconductor).
* gnu/packages/bioinformatics.scm (r-numbat): Delete variable.
Change-Id: Ic1f5d9779a594432a0dd8bd0be9059423a2f5b34
Diffstat (limited to 'gnu/packages/bioinformatics.scm')
-rw-r--r-- | gnu/packages/bioinformatics.scm | 72 |
1 files changed, 0 insertions, 72 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm index ead94ccb7e..d817fa9348 100644 --- a/gnu/packages/bioinformatics.scm +++ b/gnu/packages/bioinformatics.scm @@ -1314,78 +1314,6 @@ This approach leads to an improved gene expression profile for quantifying gene regulations.") (license license:expat)))) -(define-public r-numbat - (let ((commit "4ab7752e7d267a3f443756675728521a9b0a7295") - (revision "1")) - (package - (name "r-numbat") - (version (git-version "1.3.2-1" revision commit)) - (source (origin - (method git-fetch) - (uri (git-reference - (url "https://github.com/kharchenkolab/numbat") - (commit commit))) - (file-name (git-file-name name version)) - (sha256 - (base32 - "0wa2cz5iy570r2a57bd74jramxayvfhmxznb0vq4vyk1ia8l5jd1")))) - (properties `((upstream-name . "numbat"))) - (build-system r-build-system) - (propagated-inputs - (list r-ape - r-catools - r-data-table - r-dendextend - r-dplyr - r-genomicranges - r-ggplot2 - r-ggraph - r-ggtree - r-glue - r-igraph - r-iranges - r-logger - r-magrittr - r-matrix - r-optparse - r-paralleldist - r-patchwork - r-pryr - r-purrr - r-r-utils - r-rcpp - r-rcpparmadillo - r-rhpcblasctl - r-roptim - r-scales - r-scistreer - r-stringr - r-tibble - r-tidygraph - r-tidyr - r-vcfr - r-zoo)) - (home-page "https://github.com/kharchenkolab/numbat") - (synopsis "Haplotype-Aware CNV Analysis from scRNA-Seq") - (description - "This package provides a computational method that infers copy number -variations (CNVs) in cancer scRNA-seq data and reconstructs the tumor -phylogeny. numbat integrates signals from gene expression, allelic ratio, and -population haplotype structures to accurately infer allele-specific CNVs in -single cells and reconstruct their lineage relationship. numbat can be used -to: - -@enumerate -@item detect allele-specific copy number variations from single-cells; -@item differentiate tumor versus normal cells in the tumor microenvironment; -@item infer the clonal architecture and evolutionary history of profiled -tumors. -@end enumerate - -numbat does not require tumor/normal-paired DNA or genotype data, but operates -solely on the donor scRNA-data data (for example, 10x Cell Ranger output).") - (license license:expat)))) - (define-public r-p2data (let ((commit "7d4c0e17d7899f9d9b08ab2bf455abe150912f4c") (revision "1")) |