Cinfony – combining Open Source cheminformatics toolkits behind a common interface
<p>Abstract</p> <p>Background</p> <p>Open Source cheminformatics toolkits such as OpenBabel, the CDK and the RDKit share the same core functionality but support different sets of file formats and forcefields, and calculate different fingerprints and descriptors. Despite...
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doaj-feb231ef26af443f844e89ead1a883bc2021-08-02T09:47:47ZengBMCChemistry Central Journal1752-153X2008-12-01212410.1186/1752-153X-2-24Cinfony – combining Open Source cheminformatics toolkits behind a common interfaceHutchison Geoffrey RO'Boyle Noel M<p>Abstract</p> <p>Background</p> <p>Open Source cheminformatics toolkits such as OpenBabel, the CDK and the RDKit share the same core functionality but support different sets of file formats and forcefields, and calculate different fingerprints and descriptors. Despite their complementary features, using these toolkits in the same program is difficult as they are implemented in different languages (C++ versus Java), have different underlying chemical models and have different application programming interfaces (APIs).</p> <p>Results</p> <p>We describe Cinfony, a Python module that presents a common interface to all three of these toolkits, allowing the user to easily combine methods and results from any of the toolkits. In general, the run time of the Cinfony modules is almost as fast as accessing the underlying toolkits directly from C++ or Java, but Cinfony makes it much easier to carry out common tasks in cheminformatics such as reading file formats and calculating descriptors.</p> <p>Conclusion</p> <p>By providing a simplified interface and improving interoperability, Cinfony makes it easy to combine complementary features of OpenBabel, the CDK and the RDKit.</p> http://journal.chemistrycentral.com/content/2/1/24 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hutchison Geoffrey R O'Boyle Noel M |
spellingShingle |
Hutchison Geoffrey R O'Boyle Noel M Cinfony – combining Open Source cheminformatics toolkits behind a common interface Chemistry Central Journal |
author_facet |
Hutchison Geoffrey R O'Boyle Noel M |
author_sort |
Hutchison Geoffrey R |
title |
Cinfony – combining Open Source cheminformatics toolkits behind a common interface |
title_short |
Cinfony – combining Open Source cheminformatics toolkits behind a common interface |
title_full |
Cinfony – combining Open Source cheminformatics toolkits behind a common interface |
title_fullStr |
Cinfony – combining Open Source cheminformatics toolkits behind a common interface |
title_full_unstemmed |
Cinfony – combining Open Source cheminformatics toolkits behind a common interface |
title_sort |
cinfony – combining open source cheminformatics toolkits behind a common interface |
publisher |
BMC |
series |
Chemistry Central Journal |
issn |
1752-153X |
publishDate |
2008-12-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Open Source cheminformatics toolkits such as OpenBabel, the CDK and the RDKit share the same core functionality but support different sets of file formats and forcefields, and calculate different fingerprints and descriptors. Despite their complementary features, using these toolkits in the same program is difficult as they are implemented in different languages (C++ versus Java), have different underlying chemical models and have different application programming interfaces (APIs).</p> <p>Results</p> <p>We describe Cinfony, a Python module that presents a common interface to all three of these toolkits, allowing the user to easily combine methods and results from any of the toolkits. In general, the run time of the Cinfony modules is almost as fast as accessing the underlying toolkits directly from C++ or Java, but Cinfony makes it much easier to carry out common tasks in cheminformatics such as reading file formats and calculating descriptors.</p> <p>Conclusion</p> <p>By providing a simplified interface and improving interoperability, Cinfony makes it easy to combine complementary features of OpenBabel, the CDK and the RDKit.</p> |
url |
http://journal.chemistrycentral.com/content/2/1/24 |
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