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David J. Thomas

dblp:291/4332 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 1990
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 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 graphics and multimedia
1 paper
Multimedia analysis and retrieval · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gel electrophoresis
0.011990
Quantitative analysis of one-dimensional gel electrophoresis profiles · Comput. Appl. Biosci. 1990
Multimedia analysis and retrieval
image analysis
0.011990
Quantitative analysis of one-dimensional gel electrophoresis profiles · Comput. Appl. Biosci. 1990

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

peak-area determination · 0.0least-squares profile fitting · 0.0gaussian fitting · 0.0
YearPublicationVenuePosition
1990 Quantitative analysis of one-dimensional gel electrophoresis profiles
abstract
A general method for the one-dimensional quantitative analysis of band profiles from an autoradiographed or stained gel is described. Curved lanes may be tracked, noise across the width of the band reduced by local averaging of densities within a selected window, and background-corrected density profiles produced. Sections of each profile can be subjected to a choice of three methods of peak-area determination, depending on the type of gel and the requirements of the analysis being carried out. In the first method, simple integration is used to measure the area under the profile between any two positions. The second method integrates a Gaussian distribution fitted to a single peak. Where bands overlap, the third method resolves peaks into their component areas, taking into account the observed increase in the width of the band in the direction of electrophoretic migration. This is incorporated into a least-squares profile-fitting method, which is shown to be both accurate and efficient.
Judith M. Smith, David J. Thomas
Comput. Appl. Biosci.2