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-rw-r--r--gnu/packages/bioinformatics.scm6
1 files changed, 3 insertions, 3 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index 55a0881849..dd90887550 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -10197,7 +10197,7 @@ API services.")
(propagated-inputs
(list python-biothings-client))
(home-page "https://github.com/biothings/mygene.py")
- (synopsis "Python Client for MyGene.Info services.")
+ (synopsis "Python Client for MyGene.Info services")
(description "MyGene.Info provides simple-to-use REST web services
to query/retrieve gene annotation data. It's designed with simplicity
and performance emphasized. Mygene is a Python wrapper to access
@@ -11871,7 +11871,7 @@ implementation differs in these ways:
("python-pytest" ,python-pytest)
("python-setuptools-scm" ,python-setuptools-scm)))
(home-page "https://github.com/theislab/scanpy")
- (synopsis "Single-Cell Analysis in Python.")
+ (synopsis "Single-Cell Analysis in Python")
(description "Scanpy is a scalable toolkit for analyzing single-cell gene
expression data. It includes preprocessing, visualization, clustering,
pseudotime and trajectory inference and differential expression testing. The
@@ -15176,7 +15176,7 @@ parser for Python.")
(inputs
(list python-configparser python-pysam python-pyvcf))
(home-page "https://github.com/mroosmalen/nanosv")
- (synopsis "Structural variation detection tool for Oxford Nanopore data.")
+ (synopsis "Structural variation detection tool for Oxford Nanopore data")
(description "NanoSV is a software package that can be used to identify
structural genomic variations in long-read sequencing data, such as data
produced by Oxford Nanopore Technologies’ MinION, GridION or PromethION