Gavin C. Cawley
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Gavin C. Cawley has a total of 126 co-authors. Here are the top co-authors by number of shared publications:
N.L.C. Talbot
7 shared publicationsNicola L.C. Talbot
School of Computing Sciences, University of East Anglia, NR4 7TJ Norwich, Norfolk, UK
7 shared publicationsNicola L. C. Talbot
School of Computing Sciences, University of East Anglia, Norwich, UK
6 shared publicationsDanilo P. Mandic
Department of Electrical and Electronic Engineering, Imperial College of Science, Technology and Medicine, London SW7 2BT, UK
4 shared publicationsStephen Dorling
4 shared publicationsStephen R. Dorling
4 shared publications
Latest Publications
- Top Cited Papers
- 1 November 2021
- Published by Elsevier in Expert Systems with Applications
- Vol. 182
Nested cross-validation when selecting classifiers is overzealous for most practical applications
- 1 November 2021
- Published by Elsevier in Expert Systems with Applications
- Vol. 182
Top Cited PapersNested cross-validation when selecting classifiers is overzealous for most practical applications
- Open Access
- 9 April 2020
- Published by Springer Nature in BMC Bioinformatics
- Vol. 21 (1) , 1-18
Investigation of sequence features of hinge-bending regions in proteins with domain movements using kernel logistic regression
Background: Hinge-bending movements in proteins comprising two or more domains form a large class of functional movements. Hinge-bending regions demarcate protein domains and collectively control the domain movement. Consequently, the ability to recognise sequence features of hinge-bending regions and to be able to predict them from sequence alone would benefit various areas of protein research. For example, an understanding of how the sequence features of these regions relate to dynamic properties in multi-domain proteins would aid in the rational design of linkers in therapeutic fusion proteins. Results: The DynDom database of protein domain movements comprises sequences annotated to indicate whether the amino acid residue is located within a hinge-bending region or within an intradomain region. Using statistical methods and Kernel Logistic Regression (KLR) models, this data was used to determine sequence features that favour or disfavour hinge-bending regions. This is a difficult classification problem as the number of negative cases (intradomain residues) is much larger than the number of positive cases (hinge residues). The statistical methods and the KLR models both show that cysteine has the lowest propensity for hinge-bending regions and proline has the highest, even though it is the most rigid amino acid. As hinge-bending regions have been previously shown to occur frequently at the terminal regions of the secondary structures, the propensity for proline at these regions is likely due to its tendency to break secondary structures. The KLR models also indicate that isoleucine may act as a domain-capping residue. We have found that a quadratic KLR model outperforms a linear KLR model and that improvement in performance occurs up to very long window lengths (eighty residues) indicating long-range correlations. Conclusion: In contrast to the only other approach that focused solely on interdomain hinge-bending regions, the method provides a modest and statistically significant improvement over a random classifier. An explanation of the KLR results is that in the prediction of hinge-bending regions a long-range correlation is at play between a small number amino acids that either favour or disfavour hinge-bending regions. The resulting sequence-based prediction tool, HingeSeek, is available to run through a webserver at hingeseek.cmp.uea.ac.uk.
- 9 April 2020
- Published by Springer Nature in BMC Bioinformatics
- Vol. 21 (1) , 1-18
Open AccessInvestigation of sequence features of hinge-bending regions in proteins with domain movements using kernel logistic regression
Background: Hinge-bending movements in proteins comprising two or more domains form a large class of functional movements. Hinge-bending regions demarcate protein domains and collectively control the domain movement. Consequently, the ability to recognise sequence features of hinge-bending regions and to be able to predict them from sequence alone would benefit various areas of protein research. For example, an understanding of how the sequence features of these regions relate to dynamic properties in multi-domain proteins would aid in the rational design of linkers in therapeutic fusion proteins. Results: The DynDom database of protein domain movements comprises sequences annotated to indicate whether the amino acid residue is located within a hinge-bending region or within an intradomain region. Using statistical methods and Kernel Logistic Regression (KLR) models, this data was used to determine sequence features that favour or disfavour hinge-bending regions. This is a difficult classification problem as the number of negative cases (intradomain residues) is much larger than the number of positive cases (hinge residues). The statistical methods and the KLR models both show that cysteine has the lowest propensity for hinge-bending regions and proline has the highest, even though it is the most rigid amino acid. As hinge-bending regions have been previously shown to occur frequently at the terminal regions of the secondary structures, the propensity for proline at these regions is likely due to its tendency to break secondary structures. The KLR models also indicate that isoleucine may act as a domain-capping residue. We have found that a quadratic KLR model outperforms a linear KLR model and that improvement in performance occurs up to very long window lengths (eighty residues) indicating long-range correlations. Conclusion: In contrast to the only other approach that focused solely on interdomain hinge-bending regions, the method provides a modest and statistically significant improvement over a random classifier. An explanation of the KLR results is that in the prediction of hinge-bending regions a long-range correlation is at play between a small number amino acids that either favour or disfavour hinge-bending regions. The resulting sequence-based prediction tool, HingeSeek, is available to run through a webserver at hingeseek.cmp.uea.ac.uk.
- 1 September 2015
- Published by Elsevier in Ecological Modelling
- Vol. 312, 102-103
Corrigendum to “On a minimal model for estimating climate sensitivity” [Ecol. Model. 297 (2015) 20–25]
- 1 September 2015
- Published by Elsevier in Ecological Modelling
- Vol. 312, 102-103
Corrigendum to “On a minimal model for estimating climate sensitivity” [Ecol. Model. 297 (2015) 20–25]
- 1 July 2015
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- No. 21614393,p. 1-8
Design of the 2015 ChaLearn AutoML challenge
ChaLearn is organizing the Automatic Machine Learning (AutoML) contest for IJCNN 2015, which challenges participants to solve classification and regression problems without any human intervention. Participants' code is automatically run on the contest servers to train and test learning machines. However, there is no obligation to submit code; half of the prizes can be won by submitting prediction results only. Datasets of progressively increasing difficulty are introduced throughout the six rounds of the challenge. (Participants can enter the competition in any round.) The rounds alternate phases in which learners are tested on datasets participants have not seen, and phases in which participants have limited time to tweak their algorithms on those datasets to improve performance. This challenge will push the state of the art in fully automatic machine learning on a wide range of real-world problems. The platform will remain available beyond the termination of the challenge.
- 1 July 2015
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- No. 21614393,p. 1-8
Design of the 2015 ChaLearn AutoML challenge
ChaLearn is organizing the Automatic Machine Learning (AutoML) contest for IJCNN 2015, which challenges participants to solve classification and regression problems without any human intervention. Participants' code is automatically run on the contest servers to train and test learning machines. However, there is no obligation to submit code; half of the prizes can be won by submitting prediction results only. Datasets of progressively increasing difficulty are introduced throughout the six rounds of the challenge. (Participants can enter the competition in any round.) The rounds alternate phases in which learners are tested on datasets participants have not seen, and phases in which participants have limited time to tweak their algorithms on those datasets to improve performance. This challenge will push the state of the art in fully automatic machine learning on a wide range of real-world problems. The platform will remain available beyond the termination of the challenge.
- 1 February 2015
- Published by Elsevier in Ecological Modelling
- Vol. 297, 20-25
On a minimal model for estimating climate sensitivity
- 1 February 2015
- Published by Elsevier in Ecological Modelling
- Vol. 297, 20-25
On a minimal model for estimating climate sensitivity
- Open Access
- 30 July 2014
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 30 (22) , 3189-3196
Quantitative method for the assignment of hinge and shear mechanism in protein domain movements
Motivation: A popular method for classification of protein domain movements apportions them into two main types: those with a ‘hinge’ mechanism and those with a ‘shear’ mechanism. The intuitive assignment of domain movements to these classes has limited the number of domain movements that can be classified in this way. Furthermore, whether intended or not, the term ‘shear’ is often interpreted to mean a relative translation of the domains. Results: Numbers of occurrences of four different types of residue contact changes between domains were optimally combined by logistic regression using the training set of domain movements intuitively classified as hinge and shear to produce a predictor for hinge and shear. This predictor was applied to give a 10-fold increase in the number of examples over the number previously available with a high degree of precision. It is shown that overall a relative translation of domains is rare, and that there is no difference between hinge and shear mechanisms in this respect. However, the shear set contains significantly more examples of domains having a relative twisting movement than the hinge set. The angle of rotation is also shown to be a good discriminator between the two mechanisms. Availability and implementation: Results are free to browse at http://www.cmp.uea.ac.uk/dyndom/interface/ . Contact:sjh@cmp.uea.ac.uk . Supplementary information: Supplementary data are available at Bioinformatics online.
- 30 July 2014
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 30 (22) , 3189-3196
Open AccessQuantitative method for the assignment of hinge and shear mechanism in protein domain movements
Motivation: A popular method for classification of protein domain movements apportions them into two main types: those with a ‘hinge’ mechanism and those with a ‘shear’ mechanism. The intuitive assignment of domain movements to these classes has limited the number of domain movements that can be classified in this way. Furthermore, whether intended or not, the term ‘shear’ is often interpreted to mean a relative translation of the domains. Results: Numbers of occurrences of four different types of residue contact changes between domains were optimally combined by logistic regression using the training set of domain movements intuitively classified as hinge and shear to produce a predictor for hinge and shear. This predictor was applied to give a 10-fold increase in the number of examples over the number previously available with a high degree of precision. It is shown that overall a relative translation of domains is rare, and that there is no difference between hinge and shear mechanisms in this respect. However, the shear set contains significantly more examples of domains having a relative twisting movement than the hinge set. The angle of rotation is also shown to be a good discriminator between the two mechanisms. Availability and implementation: Results are free to browse at http://www.cmp.uea.ac.uk/dyndom/interface/ . Contact:sjh@cmp.uea.ac.uk . Supplementary information: Supplementary data are available at Bioinformatics online.
- 1 May 2014
- Published by Elsevier in Neural Networks
- Vol. 53, 69-80
Kernel learning at the first level of inference
- 1 May 2014
- Published by Elsevier in Neural Networks
- Vol. 53, 69-80
Kernel learning at the first level of inference
- Open Access
- 18 November 2013
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 8 (11) , e81224
Classification of Domain Movements in Proteins Using Dynamic Contact Graphs
A new method for the classification of domain movements in proteins is described and applied to 1822 pairs of structures from the Protein Data Bank that represent a domain movement in two-domain proteins. The method is based on changes in contacts between residues from the two domains in moving from one conformation to the other. We argue that there are five types of elemental contact changes and that these relate to five model domain movements called: “free”, “open-closed”, “anchored”, “sliding-twist”, and “see-saw.” A directed graph is introduced called the “Dynamic Contact Graph” which represents the contact changes in a domain movement. In many cases a graph, or part of a graph, provides a clear visual metaphor for the movement it represents and is a motif that can be easily recognised. The Dynamic Contact Graphs are often comprised of disconnected subgraphs indicating independent regions which may play different roles in the domain movement. The Dynamic Contact Graph for each domain movement is decomposed into elemental Dynamic Contact Graphs, those that represent elemental contact changes, allowing us to count the number of instances of each type of elemental contact change in the domain movement. This naturally leads to sixteen classes into which the 1822 domain movements are classified.
- 18 November 2013
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 8 (11) , e81224
Open AccessClassification of Domain Movements in Proteins Using Dynamic Contact Graphs
A new method for the classification of domain movements in proteins is described and applied to 1822 pairs of structures from the Protein Data Bank that represent a domain movement in two-domain proteins. The method is based on changes in contacts between residues from the two domains in moving from one conformation to the other. We argue that there are five types of elemental contact changes and that these relate to five model domain movements called: “free”, “open-closed”, “anchored”, “sliding-twist”, and “see-saw.” A directed graph is introduced called the “Dynamic Contact Graph” which represents the contact changes in a domain movement. In many cases a graph, or part of a graph, provides a clear visual metaphor for the movement it represents and is a motif that can be easily recognised. The Dynamic Contact Graphs are often comprised of disconnected subgraphs indicating independent regions which may play different roles in the domain movement. The Dynamic Contact Graph for each domain movement is decomposed into elemental Dynamic Contact Graphs, those that represent elemental contact changes, allowing us to count the number of instances of each type of elemental contact change in the domain movement. This naturally leads to sixteen classes into which the 1822 domain movements are classified.
- 1 January 2012
- Published by Springer Nature in Lecture Notes in Computer Science
- p. 1
Over-Fitting in Model Selection and Its Avoidance
- 1 January 2012
- Published by Springer Nature in Lecture Notes in Computer Science
- p. 1
Over-Fitting in Model Selection and Its Avoidance
- 26 September 2011
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 25 (11) , 5503-5513
On the Atmospheric Residence Time of Anthropogenically Sourced Carbon Dioxide
- 26 September 2011
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 25 (11) , 5503-5513
On the Atmospheric Residence Time of Anthropogenically Sourced Carbon Dioxide