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authorRicardo Wurmus <rekado@elephly.net>2024-11-28 11:34:48 +0100
committerRicardo Wurmus <rekado@elephly.net>2024-12-03 16:59:56 +0100
commite3bbf678e374a255bb0f97793c3a90fc799f53d0 (patch)
tree242203c10ebab3837302550e9ef0cfed9b3b8cd4 /gnu/packages/bioinformatics.scm
parentdff6f586884a35d6531437f42f4425cb844634fa (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.scm72
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"))