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