Full metadata record
DC FieldValueLanguage
dc.contributor.authorChen, Chianen_US
dc.contributor.authorWang, Hsiuyingen_US
dc.date.accessioned2019-10-05T00:08:41Z-
dc.date.available2019-10-05T00:08:41Z-
dc.date.issued1970-01-01en_US
dc.identifier.issn1066-5277en_US
dc.identifier.urihttp://dx.doi.org/10.1089/cmb.2019.0232en_US
dc.identifier.urihttp://hdl.handle.net/11536/152805-
dc.description.abstractProtein-based virtual screening is integral to the modern drug discovery process. Most protein-based virtual screening experiments are performed using docking programs. The accuracy of a docking program strongly relies on the incorporated scoring function used, which is based on various energy terms. The existing scoring functions deal with the energy terms that use the equal weight function or other weight functions, which do not depend on characteristics of the protein. To improve the existing methods, Lu and Wang proposed a protein-specific scoring function based on a regression analysis that was shown to have higher performance than the existing methods. In this study, we propose a protein-specific scoring approach to select potential ligands based on logistic regression analysis. The performance of our method was evaluated using the Directory of Useful Decoys docked data set, which contains 40 protein targets. The results showed that the proposed method can increase the enrichment factors for most of the 40 protein targets.en_US
dc.language.isoen_USen_US
dc.subjectdockingen_US
dc.subjectlogistic regressionen_US
dc.subjectprotein-specific scoring methoden_US
dc.titleLogistic Regression Method for Ligand Discoveryen_US
dc.typeArticleen_US
dc.identifier.doi10.1089/cmb.2019.0232en_US
dc.identifier.journalJOURNAL OF COMPUTATIONAL BIOLOGYen_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department統計學研究所zh_TW
dc.contributor.departmentInstitute of Statisticsen_US
dc.identifier.wosnumberWOS:000487270600001en_US
dc.citation.woscount0en_US
Appears in Collections:Articles