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High-Throughput Screening Assays in Toxicology

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Cover of 'High-Throughput Screening Assays in Toxicology'

Table of Contents

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    Book Overview
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    Chapter 1 Monitoring Ligand-Activated Protein–Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay
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    Chapter 2 Mitochondrial Membrane Potential Assay
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    Chapter 3 High-Throughput Screening Assays in Toxicology
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    Chapter 4 Quantitative High-Throughput Luciferase Screening in Identifying CAR Modulators
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    Chapter 5 Transactivation and Coactivator Recruitment Assays for Measuring Farnesoid X Receptor Activity
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    Chapter 6 Cell-Based Assay for Identifying the Modulators of Antioxidant Response Element Signaling Pathway
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    Chapter 7 Study Liver Cytochrome P450 3A4 Inhibition and Hepatotoxicity Using DMSO-Differentiated HuH-7 Cells
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    Chapter 8 Determination of Histone H2AX Phosphorylation in DT40 Cells
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    Chapter 9 High-Throughput and High-Content Micronucleus Assay in CHO-K1 Cells
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    Chapter 10 High-Throughput Screening Assays in Toxicology
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    Chapter 11 High-Throughput Screening Assays in Toxicology
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    Chapter 12 A Quantitative High-Throughput Screening Data Analysis Pipeline for Activity Profiling
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    Chapter 13 Correction of Microplate Data from High-Throughput Screening
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    Chapter 14 CurveP Method for Rendering High-Throughput Screening Dose-Response Data into Digital Fingerprints
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    Chapter 15 Accounting Artifacts in High-Throughput Toxicity Assays
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    Chapter 16 Accessing the High-Throughput Screening Data Landscape
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    Chapter 17 Curating and Preparing High-Throughput Screening Data for Quantitative Structure-Activity Relationship Modeling
Attention for Chapter 14: CurveP Method for Rendering High-Throughput Screening Dose-Response Data into Digital Fingerprints
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Chapter title
CurveP Method for Rendering High-Throughput Screening Dose-Response Data into Digital Fingerprints
Chapter number 14
Book title
High-Throughput Screening Assays in Toxicology
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6346-1_14
Pubmed ID
Book ISBNs
978-1-4939-6344-7, 978-1-4939-6346-1
Authors

Alexander Sedykh, Sedykh, Alexander

Abstract

The nature of high-throughput screening (HTS) puts certain limits on optimal test conditions for each particular sample, therefore, on top of usual data normalization, additional parsing is often needed to account for incomplete read outs or various artifacts that arise from signal interferences.CurveP is a heuristic, user-tunable, curve-cleaning algorithm that attempts to find a minimum set of corrections, which would give a monotonic dose-response curve. After applying the corrections, the algorithm proceeds to calculate a set of numeric features, which can be used as a fingerprint characterizing the sample, or as a vector of independent variables (e.g., molecular descriptors in case of chemical substances testing). The resulting output can be a part of HTS data analysis or can be used as input for a broad spectrum of computational applications, such as Quantitative Structure-Activity Relationship (QSAR) modeling, computational toxicology, bio- and cheminformatics.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 75%
Unknown 1 25%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 1 25%
Computer Science 1 25%
Agricultural and Biological Sciences 1 25%
Unknown 1 25%