branch master updated: gnu: r-catalyst: Update description.

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     new 7d990e775e gnu: r-catalyst: Update description.
7d990e775e is described below

commit 7d990e775e76c0a898c7d4b53691d1932fc0e6eb
Author: Mădălin Ionel Patrașcu <madalinionel.patrascu@mdc-berlin.de>
AuthorDate: Wed Apr 13 13:21:03 2022 +0200

    gnu: r-catalyst: Update description.
    
    * gnu/packages/bioconductor.scm (r-catalyst)[description]: Add Texinfo 
markup
    and clarify a sentence.
    
    Signed-off-by: Ricardo Wurmus <rekado@elephly.net>
---
 gnu/packages/bioconductor.scm | 29 +++++++++++++++++------------
 1 file changed, 17 insertions(+), 12 deletions(-)

diff --git a/gnu/packages/bioconductor.scm b/gnu/packages/bioconductor.scm
index b492214971..1401053570 100644
--- a/gnu/packages/bioconductor.scm
+++ b/gnu/packages/bioconductor.scm
@@ -13791,20 +13791,25 @@ relevant, and the minimum expression of the most 
abundant condition.")
             r-summarizedexperiment))
     (native-inputs
      (list r-knitr))
-    (home-page
-      "https://github.com/HelenaLC/CATALYST";)
+    (home-page "https://github.com/HelenaLC/CATALYST";)
     (synopsis "Cytometry data analysis tools")
     (description
-      "This package is Cytometry dATa anALYSis Tools (CATALYST).  Mass
-cytometry (CyTOF) uses heavy metal isotopes rather than fluorescent tags as
-reporters to label antibodies, thereby substantially decreasing spectral
-overlap and allowing for examination of over 50 parameters at the single cell
-level.  While spectral overlap is significantly less pronounced in CyTOF than
-flow cytometry, spillover due to detection sensitivity, isotopic impurities,
-and oxide formation can impede data interpretability.  We designed
-CATALYST (Cytometry dATa anALYSis Tools) to provide a pipeline for
-preprocessing of cytometry data, including i) normalization using bead
-standards, ii) single-cell deconvolution, and iii) bead-based compensation.")
+     "This package is @dfn{Cytometry dATa anALYSis Tools} (CATALYST).  Mass
+cytometry like @dfn{Cytometry by time of flight} (CyTOF) uses heavy metal
+isotopes rather than fluorescent tags as reporters to label antibodies,
+thereby substantially decreasing spectral overlap and allowing for examination
+of over 50 parameters at the single cell level.  While spectral overlap is
+significantly less pronounced in CyTOF than flow cytometry, spillover due to
+detection sensitivity, isotopic impurities, and oxide formation can impede
+data interpretability.  @code{CATALYST} was designed to provide a pipeline for
+preprocessing of cytometry data, including:
+
+@enumerate
+@item normalization using bead standards;
+@item single-cell deconvolution;
+@item bead-based compensation.
+@end enumerate
+")
     (license license:gpl2+)))
 
 (define-public r-erma