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Daniel L. Barton

dblp:36/2360 · DBLP profile ↗
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4ranked-venue papers
2as first author
1since 2021 · last 2024
0000-0002-8386-3201ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 3 · 2 first-author · 1 since 2021Systems, architecture and hardware · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
Cloud and datacenter computing · 100%

Topics — the 7 heaviest of 7, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
multiple sequence alignment
0.312018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Bioinformatics and computational biology › protein structure prediction
protein disorder prediction
0.312018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Bioinformatics and computational biology
protein structure prediction
0.312018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Bioinformatics and computational biology › RNA biology › RNA analysis › RNA bioinformatics › RNA structure prediction
RNA secondary structure prediction
0.312018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Bioinformatics and computational biology
sequence analysis
0.312018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Cloud and datacenter computing › cluster resource management and scheduling
cluster resource management
0.112018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018
Cloud and datacenter computing
job scheduling
0.112018
JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure · Bioinform. 2018

Methods — techniques the papers use, named apart from their topics

web services · 0.7
YearPublicationVenuePosition
2024 Data-driven modelling makes quantitative predictions regarding bacteria surface motility
abstract
In this work, we quantitatively compare computer simulations and existing cell tracking data of P. aeruginosa surface motility in order to analyse the underlying motility mechanism. We present a three dimensional twitching motility model, that simulates the extension, retraction and surface association of individual Type IV Pili (TFP), and is informed by recent experimental observations of TFP. Sensitivity analysis is implemented to minimise the number of model parameters, and quantitative estimates for the remaining parameters are inferred from tracking data by approximate Bayesian computation. We argue that the motility mechanism is highly sensitive to experimental conditions. We predict a TFP retraction speed for the tracking data we study that is in a good agreement with experimental results obtained under very similar conditions. Furthermore, we examine whether estimates for biologically important parameters, whose direct experimental determination is challenging, can be inferred directly from tracking data. One example is the width of the distribution of TFP on the bacteria body. We predict that the TFP are broadly distributed over the bacteria pole in both walking and crawling motility types. Moreover, we identified specific configurations of TFP that lead to transitions between walking and crawling states.
Daniel L. Barton, Yow-Ren Chang, William Ducker, Jure Dobnikar
PLoS Comput. Biol.1
2018 JABAWS 2.2 distributed web services for Bioinformatics: protein disorder, conservation and RNA secondary structure
abstract
Summary: JABAWS 2.2 is a computational framework that simplifies the deployment of web services for Bioinformatics. In addition to the five multiple sequence alignment (MSA) algorithms in JABAWS 1.0, JABAWS 2.2 includes three additional MSA programs (Clustal Omega, MSAprobs, GLprobs), four protein disorder prediction methods (DisEMBL, IUPred, Ronn, GlobPlot), 18 measures of protein conservation as implemented in AACon, and RNA secondary structure prediction by the RNAalifold program. JABAWS 2.2 can be deployed on a variety of in-house or hosted systems. JABAWS 2.2 web services may be accessed from the Jalview multiple sequence analysis workbench (Version 2.8 and later), as well as directly via the JABAWS command line interface (CLI) client. JABAWS 2.2 can be deployed on a local virtual server as a Virtual Appliance (VA) or simply as a Web Application Archive (WAR) for private use. Improvements in JABAWS 2.2 also include simplified installation and a range of utility tools for usage statistics collection, and web services querying and monitoring. The JABAWS CLI client has been updated to support all the new services and allow integration of JABAWS 2.2 services into conventional scripts. A public JABAWS 2 server has been in production since December 2011 and served over 800 000 analyses for users worldwide. Availability and implementation: JABAWS 2.2 is made freely available under the Apache 2 license and can be obtained from: http://www.compbio.dundee.ac.uk/jabaws. Contact: [email protected].
Peter V. Troshin, James B. Procter, Alexander Sherstnev, Daniel L. Barton, Fábio Madeira, Geoffrey J. Barton
Bioinform.4
2017 Active Vertex Model for cell-resolution description of epithelial tissue mechanics
Daniel L. Barton, Silke Henkes, Cornelis J. Weijer, Rastko Sknepnek
PLoS Comput. Biol.1
1997 Transient Power Supply Voltage (VDDT) Analysis for Detecting IC Defects
abstract
Transient power supply voltage (V/sub DDT/) analysis is a new testing technique demonstrated as a powerful alternative and complement to I/sub DDQ/ testing. V/sub DDT/ analysis takes advantage of the limited response time of a voltage supply to the changing power demand of an IC during operation. Changes in the V/sub DD/ response time can be used to detect increases in the power demand of a microcontroller with resolutions of 20 nA at 100 kHz, 1 /spl mu/A at 1 MHz, and 2.5 /spl mu/A at 1.5 MHz. These current sensitivities have been shown for ICs with very low I/sub DDQ/ (300 /spl mu/A. The present system uses 100 cycle averaging to compensate for low frequency "jitter". The V/sub DDT/ signal acquisition protocols, frequency versus sensitivity tradeoffs, hardware considerations, noise limitations, data examples, and areas for future research are described.
Edward I. Cole Jr., Jerry M. Soden, Paiboon Tangyunyong, Patrick L. Candelaria, Richard W. Beegle, Daniel L. Barton, Christopher L. Henderson, Charles F. Hawkins
ITC6