SDRS—an algorithm for analyzing large-scale dose–response data

Dose–response information is critical to understanding drug effects, yet analytical methods for dose–response assays cannot cope with the dimensionality of large-scale screening data such as the microarray profiling data. To overcome this limitation, we developed and implemented the Sigmoidal Dose R...

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Bibliographic Details
Published inBioinformatics Vol. 27; no. 20; pp. 2921 - 2923
Main Authors Ji, Rui-Ru, Siemers, Nathan O, Lei, Ming, Schweizer, Liang, Bruccoleri, Robert E
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 15.10.2011
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ISSN1367-4803
1367-4811
1367-4811
1460-2059
DOI10.1093/bioinformatics/btr489

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Summary:Dose–response information is critical to understanding drug effects, yet analytical methods for dose–response assays cannot cope with the dimensionality of large-scale screening data such as the microarray profiling data. To overcome this limitation, we developed and implemented the Sigmoidal Dose Response Search (SDRS) algorithm, a grid search-based method designed to handle large-scale dose–response data. This method not only calculates the pharmacological parameters for every assay, but also provides built-in statistic that enables downstream systematic analyses, such as characterizing dose response at the transcriptome level. AVAILABILITY: Bio::SDRS is freely available from CPAN (www.cpan.org). CONTACTS: ruiruji@gmail.com; bruc@acm.org Supplementary Information: Supplementary data is available at Bioinformatics online.
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Associate Editor: Jonathan Wren
ISSN:1367-4803
1367-4811
1367-4811
1460-2059
DOI:10.1093/bioinformatics/btr489