Control: tags 872246 + patch
Control: tags 872246 + pending
Dear maintainer,
I've prepared an NMU for rdkit (versioned as 201603.5-2.1) and uploaded
it to DELAYED/10. Please feel free to tell me if I should cancel it.
cu
Adrian
--
"Is there not promise of rain?" Ling Tan asked suddenly out
of the darkness. There had been need of rain for many days.
"Only a promise," Lao Er said.
Pearl S. Buck - Dragon Seed
diff -Nru rdkit-201603.5/debian/changelog rdkit-201603.5/debian/changelog
--- rdkit-201603.5/debian/changelog 2016-11-07 14:16:00.000000000 +0200
+++ rdkit-201603.5/debian/changelog 2017-10-17 16:38:20.000000000 +0300
@@ -1,3 +1,12 @@
+rdkit (201603.5-2.1) unstable; urgency=medium
+
+ * Non-maintainer upload.
+ * Add the build dependency on latexmk required with Sphinx 1.6.
+ (Closes: #872246)
+ * Fix a typo in the package descriptions.
+
+ -- Adrian Bunk <b...@debian.org> Tue, 17 Oct 2017 16:38:20 +0300
+
rdkit (201603.5-2) unstable; urgency=medium
* Team upload.
diff -Nru rdkit-201603.5/debian/control rdkit-201603.5/debian/control
--- rdkit-201603.5/debian/control 2016-11-07 13:50:00.000000000 +0200
+++ rdkit-201603.5/debian/control 2017-10-17 16:38:20.000000000 +0300
@@ -22,6 +22,7 @@
python-numpy,
python-pandas,
python-sphinx,
+ latexmk,
texlive-fonts-recommended,
texlive-generic-extra,
texlive-latex-base,
@@ -60,7 +61,7 @@
* Chirality support, including calculation of (R/S) stereochemistry codes
* 2D pharmacophore searching
* Fingerprinting, including Daylight-like, atom pairs, topological
- torsions, Morgan alogrithm and MACCS keys
+ torsions, Morgan algorithm and MACCS keys
* Calculation of shape similarity
* Multi-molecule maximum common substructure
* Machine-learning via clustering and information theory algorithms
@@ -109,7 +110,7 @@
* Chirality support, including calculation of (R/S) stereochemistry codes
* 2D pharmacophore searching
* Fingerprinting, including Daylight-like, atom pairs, topological
- torsions, Morgan alogrithm and MACCS keys
+ torsions, Morgan algorithm and MACCS keys
* Calculation of shape similarity
* Multi-molecule maximum common substructure
* Machine-learning via clustering and information theory algorithms
@@ -141,7 +142,7 @@
* Chirality support, including calculation of (R/S) stereochemistry codes
* 2D pharmacophore searching
* Fingerprinting, including Daylight-like, atom pairs, topological
- torsions, Morgan alogrithm and MACCS keys
+ torsions, Morgan algorithm and MACCS keys
* Calculation of shape similarity
* Multi-molecule maximum common substructure
* Machine-learning via clustering and information theory algorithms
