Literature DB >> 19551358

Statistics and decision making in high-throughput screening.

Isabel Coma1, Jesus Herranz, Julio Martin.   

Abstract

Screening is about making decisions on the modulating activity of one particular compound on a biological system. When a compound testing experiment is repeated under the same conditions or as close to the same conditions as possible, the observed results are never exactly the same, and there is an apparent random and uncontrolled source of variability in the system under study. Nevertheless, randomness is not haphazard. In this context, we can see statistics as the science of decision making under uncertainty. Thus, the usage of statistical tools in the analysis of screening experiments is the right approach to the interpretation of screening data, with the aim of making them meaningful and converting them into valuable information that supports sound decision making.In the HTS workflow, there are at least three key stages where key decisions have to be made based on experimental data: (1) assay development (i.e. how to assess whether our assay is good enough to be put into screening production for the identification of modulators of the target of interest), (2) HTS campaign process (i.e. monitoring that screening process is performing at the expected quality and assessing possible patterned signs of experimental response that may adversely bias and mislead hit identification) and (3) data analysis of primary HTS data (i.e. flagging which compounds are giving a positive response in the assay, namely hit identification).In this chapter we will focus on how some statistical tools can help to cope with these three aspects. Assessment of assay quality is reviewed in other chapters, so in Section 1 we will briefly make some further considerations. Section 2 will review statistical process control, Section 3 will cover methodologies for detecting and dealing with HTS patterns and Section 4 will describe approaches for statistically guided selection of hits in HTS.

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Year:  2009        PMID: 19551358     DOI: 10.1007/978-1-60327-258-2_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

Review 1.  Design and implementation of high throughput screening assays.

Authors:  Ricardo Macarrón; Robert P Hertzberg
Journal:  Mol Biotechnol       Date:  2011-03       Impact factor: 2.695

2.  Automated selection of regions of interest for intensity-based FRET analysis of transferrin endocytic trafficking in normal vs. cancer cells.

Authors:  Ronak Talati; Andrew Vanderpoel; Amina Eladdadi; Kate Anderson; Ken Abe; Margarida Barroso
Journal:  Methods       Date:  2013-08-28       Impact factor: 3.608

3.  Imaging-based high-throughput screening assay to identify new molecules with transmission-blocking potential against Plasmodium falciparum female gamete formation.

Authors:  Celia Miguel-Blanco; Joël Lelièvre; Michael J Delves; Ana I Bardera; Jesús L Presa; María José López-Barragán; Andrea Ruecker; Sara Marques; Robert E Sinden; Esperanza Herreros
Journal:  Antimicrob Agents Chemother       Date:  2015-03-23       Impact factor: 5.191

4.  In Vitro Activity Assays for MYST Histone Acetyltransferases and Adaptation for High-Throughput Inhibitor Screening.

Authors:  C E McCullough; R Marmorstein
Journal:  Methods Enzymol       Date:  2016-02-23       Impact factor: 1.600

5.  Development and Implementation of a High Throughput Screen for the Human Sperm-Specific Isoform of Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDHS).

Authors:  Jonathan Z Sexton; Polina V Danshina; David R Lamson; Mark Hughes; Alan J House; Li-An Yeh; Deborah A O'Brien; Kevin P Williams
Journal:  Curr Chem Genomics       Date:  2011-07-04

6.  Release of 50 new, drug-like compounds and their computational target predictions for open source anti-tubercular drug discovery.

Authors:  María Jose Rebollo-Lopez; Joël Lelièvre; Daniel Alvarez-Gomez; Julia Castro-Pichel; Francisco Martínez-Jiménez; George Papadatos; Vinod Kumar; Gonzalo Colmenarejo; Grace Mugumbate; Mark Hurle; Vanessa Barroso; Rob J Young; María Martinez-Hoyos; Rubén González del Río; Robert H Bates; Eva Maria Lopez-Roman; Alfonso Mendoza-Losana; James R Brown; Emilio Alvarez-Ruiz; Marc A Marti-Renom; John P Overington; Nicholas Cammack; Lluís Ballell; David Barros-Aguire
Journal:  PLoS One       Date:  2015-12-07       Impact factor: 3.240

7.  A key mammalian cholesterol synthesis enzyme, squalene monooxygenase, is allosterically stabilized by its substrate.

Authors:  Hiromasa Yoshioka; Hudson W Coates; Ngee Kiat Chua; Yuichi Hashimoto; Andrew J Brown; Kenji Ohgane
Journal:  Proc Natl Acad Sci U S A       Date:  2020-03-13       Impact factor: 11.205

  7 in total

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