Abstract
HTS remains at the core of the drug discovery process, and so it is critical to design and implement HTS assays in a comprehensive fashion involving scientists from the disciplines of biology, chemistry, engineering, and informatics. This requires careful consideration of many options and variables, starting with the choice of screening strategy and ending with the discovery of lead compounds. At every step in this process, there are decisions to be made that can greatly impact the outcome of the HTS effort, to the point of making it a success or a failure. Although specific guidelines should be established to ensure that the screening assay reaches an acceptable level of quality, many choices require pragmatism and the ability to compromise opposing forces.
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Acknowledgements
The authors are grateful to the many colleagues at GlaxoSmithKline past and present who helped over the years to shape the screening process and to build the collective knowledge succinctly described in this introduction.
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Powell, D.J., Hertzberg, R.P., Macarrόn, R. (2016). Design and Implementation of High-Throughput Screening Assays. In: Janzen, W. (eds) High Throughput Screening. Methods in Molecular Biology, vol 1439. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3673-1_1
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DOI: https://doi.org/10.1007/978-1-4939-3673-1_1
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