D
David Clarke
Researcher at University of Edinburgh
Publications - 522
Citations - 26522
David Clarke is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Adaptive control & Model predictive control. The author has an hindex of 70, co-authored 504 publications receiving 24626 citations. Previous affiliations of David Clarke include RMIT University & Massachusetts Institute of Technology.
Papers
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Journal ArticleDOI
Sensor, actuator, and loop validation
TL;DR: In this paper, the authors discuss validation features which are best embedded in local devices and discuss generic validation and its reporting to the "next level up" for advanced control of distributed Fieldbus devices.
Journal ArticleDOI
Generalised predictive control with end-point state weighting
H. Demircioglu,David Clarke +1 more
TL;DR: Generalized predictive control with end-point state weighting is an extension of generalised predictive control (GPC) by including a weighting of the state vector at the end of the receding time frame as discussed by the authors.
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Modelling and tracking a vortex flow-meter signal
T. Ghaoud,David Clarke +1 more
TL;DR: In this article, the authors provide and verify a simulation model of the overall signal, so that different frequency-tracking methods can be compared and evaluate the performance of a zero-crossing algorithm.
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A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS
TL;DR: It would appear that haploid insufficiency or gain of function are more subtle contributors than gender‐specific genomic imprinting in the production of the PWS phenotype.
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Structural and functional studies of the biotin protein ligase from Aquifex aeolicus reveal a critical role for a conserved residue in target specificity.
Cécile Tron,Iain W. McNae,Margaret Nutley,David Clarke,Alan Cooper,Malcolm D. Walkinshaw,Robert Baxter,Dominic J. Campopiano +7 more
TL;DR: The structure of the mutant AaBPL R40G in both the ligand-free and biotin-bound forms reveals that the mutated loop has collapsed, thus hindering ATP binding, and the binding of biotin and ATP has been determined to occur via a random but cooperative process.