Literature DB >> 23878407

Analysis of High-Dimensional Structure-Activity Screening Datasets Using the Optimal Bit String Tree.

Ke Zhang1, Jacqueline M Hughes-Oliver, S Stanley Young.   

Abstract

A new classification method called the Optimal Bit String Tree is proposed to identify quantitative structure-activity relationships (QSARs). The method introduces the concept of a chromosome to describe the presence/absence context of a combination of descriptors. A descriptor set and its optimal chromosome form the splitting variable. A new stochastic searching scheme that contains a weighted sampling scheme, simulated annealing, and a trimming procedure optimizes the choice of splitting variable. Simulation studies and an application to screening monoamine oxidase (MAO) inhibitors show that OBSTree is advantageous in accurately and effectively identifying QSAR rules and finding different classes of active compounds. Details of the algorithm, SAS code, and simulated and real datasets are available online as supplementary materials.

Entities:  

Keywords:  Classification; Drug discovery; High throughput screening; Prediction; QSAR; Simulated annealing

Year:  2013        PMID: 23878407      PMCID: PMC3714111          DOI: 10.1080/00401706.2012.760489

Source DB:  PubMed          Journal:  Technometrics        ISSN: 0040-1706


  13 in total

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Authors:  X Chen; A Rusinko; A Tropsha; S S Young
Journal:  J Chem Inf Comput Sci       Date:  1999 Sep-Oct

2.  Analysis of a large structure/biological activity data set using recursive partitioning.

Authors:  A Rusinko; M W Farmen; C G Lambert; P L Brown; S S Young
Journal:  J Chem Inf Comput Sci       Date:  1999 Nov-Dec

3.  Accurate partitioning of compounds belonging to diverse activity classes.

Authors:  Ling Xue; Jürgen Bajorath
Journal:  J Chem Inf Comput Sci       Date:  2002 May-Jun

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Journal:  Science       Date:  1983-05-13       Impact factor: 47.728

5.  Analysis of a 2(9) full factorial chemical library.

Authors:  S S Young; D M Hawkins
Journal:  J Med Chem       Date:  1995-07-07       Impact factor: 7.446

Review 6.  New assay technologies for high-throughput screening.

Authors:  L Silverman; R Campbell; J R Broach
Journal:  Curr Opin Chem Biol       Date:  1998-06       Impact factor: 8.822

Review 7.  High-throughput screening: advances in assay technologies.

Authors:  G S Sittampalam; S D Kahl; W P Janzen
Journal:  Curr Opin Chem Biol       Date:  1997-10       Impact factor: 8.822

8.  The structure of the covalent adduct formed by the interaction of 3-dimethylamino-1-propyne and the flavine of mitochondrial amine oxidase.

Authors:  A L Maycock; R H Abeles; J I Salach; T P Singer
Journal:  Biochemistry       Date:  1976-01-13       Impact factor: 3.162

9.  On the significance of clusters in the graphical display of structure-activity data.

Authors:  J W McFarland; D J Gans
Journal:  J Med Chem       Date:  1986-04       Impact factor: 7.446

10.  Experimental screening of dihydrofolate reductase yields a "test set" of 50,000 small molecules for a computational data-mining and docking competition.

Authors:  Nadine H Elowe; Jan E Blanchard; Jonathan D Cechetto; Eric D Brown
Journal:  J Biomol Screen       Date:  2005-09-16
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