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authorAndreas Enge <andreas@enge.fr>2025-03-28 10:52:48 +0100
committerAndreas Enge <andreas@enge.fr>2025-04-29 11:34:51 +0200
commit743123249648baaa911eb3aecccfb232ddf3e4d8 (patch)
treebae742d1b12a8c038c79d72aeb1d93cb159d398e
parentb3a5bd2ce5f58d38e5488d7f600d983f4c7c6deb (diff)
downloadguix-743123249648baaa911eb3aecccfb232ddf3e4d8.tar.gz
guix-743123249648baaa911eb3aecccfb232ddf3e4d8.zip
gnu: Remove variant-tools.
The package does not compile any more and has no dependent packages. The last release dates from 2020; there is an additional commit in 2022; the git repository has been archived in 2023. * gnu/packages/bioinformatics.scm (variant-tools): Delete variable. Change-Id: Idb5df024121c5085f764f179d31ac67cff3fc5c7
-rw-r--r--gnu/packages/bioinformatics.scm37
1 files changed, 0 insertions, 37 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index 74cf9b0bf5..7523706358 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -15510,43 +15510,6 @@ samples into a single report. It contains modules for a large number of
common bioinformatics tools.")
(license license:gpl3+)))
-(define-public variant-tools
- (package
- (name "variant-tools")
- (version "3.1.2")
- (source
- (origin
- (method git-fetch)
- (uri (git-reference
- (url "https://github.com/vatlab/varianttools")
- ;; There is no tag corresponding to version 3.1.2
- (commit "813ae4a90d25b69abc8a40f4f70441fe09015249")))
- (file-name (git-file-name name version))
- (sha256
- (base32
- "12ibdmksj7icyqhks4xyvd61bygk4pjmxn618kp6vgk1af01y34g"))))
- (build-system python-build-system)
- (inputs
- (list boost
- c-blosc
- gsl
- hdf5
- hdf5-blosc
- python-cython
- zlib))
- (propagated-inputs
- (list python-numpy python-pycurl python-pyzmq python-scipy
- python-tables))
- (home-page "https://vatlab.github.io/vat-docs/")
- (synopsis "Analyze genetic variants from Next-Gen sequencing studies")
- (description
- "Variant tools is a tool for the manipulation, annotation,
-selection, simulation, and analysis of variants in the context of next-gen
-sequencing analysis. Unlike some other tools used for next-gen sequencing
-analysis, variant tools is project based and provides a whole set of tools to
-manipulate and analyze genetic variants.")
- (license license:gpl3+)))
-
(define-public r-chromvarmotifs
(let ((commit "38bed559c1f4770b6c91c80bf3f8ea965da26076")
(revision "1"))