Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

M. Gibson

dblp:39/6566 · DBLP profile ↗
← Back
2ranked-venue papers
0as first author
0since 2021 · last 2001
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2

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
2 papers
Bioinformatics and computational biology · 100%
Databases, data mining, and information retrieval
1 paper
Data models and query languages · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological database
gene expression database
0.012001
A relational schema for both array-based and SAGE gene expression experiments · Bioinform. 2001
Bioinformatics and computational biology › genomics
genome visualization
0.011999
bioWidgets: data interaction components for genomics · Bioinform. 1999
Bioinformatics and computational biology
genomics
0.011999
bioWidgets: data interaction components for genomics · Bioinform. 1999
Data models and query languages › relational model
relational schema
0.012001
A relational schema for both array-based and SAGE gene expression experiments · Bioinform. 2001

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

ontology-based sample description · 0.1model-view-controller · 0.0javabean · 0.0
YearPublicationVenuePosition
2001 A relational schema for both array-based and SAGE gene expression experiments
abstract
Abstract Motivation and Results: A relational schema is described for capturing highly parallel gene expression experiments using different technologies. This schema grew out of efforts to build a database for collaborators working on different biological systems and using different types of platforms in their gene expression experiments as well as different types of image quantification software. The tables are conceptually organized into three categories of information: Platform, Experiment (which includes image scanning and quantification), and Data. The strengths of the schema are: (i) integrating information on array elements using a gene index; (ii) describing samples using ontologies; (iii) reducing an experiment to a single RNA source for precise descriptions yet not losing the relationships between experiments done at the same time or for the same project; and (iv) maintaining both raw and processed (e.g. cleansed and normalized) data and recording how the data is processed. The result is a novel schema, which can hold both array and non-array data, is extensible for detailed experimental descriptions that are precise and consistent, and allows for meaningful comparisons of genes between experiments. Availability: The schema is available at http://www.cbil.upenn.edu/cgi-bin/RAD2/schemaBrowserRAD.pl. Contact: [email protected] * To whom correspondence should be addressed. 2 Present address: Department of Molecular Cell Biology, Weizmann Institute of Science, Israel.
Christian J. Stoeckert Jr., Angel D. Pizarro, Elisabetta Manduchi, M. Gibson, Brian P. Brunk, Jonathan Crabtree, Jonathan Schug, Shai Shen-Orr, G. Christian Overton
Bioinform.4
1999 bioWidgets: data interaction components for genomics
abstract
MOTIVATION: The presentation of genomics data in a perspicuous visual format is critical for its rapid interpretation and validation. Relatively few public database developers have the resources to implement sophisticated front-end user interfaces themselves. Accordingly, these developers would benefit from a reusable toolkit of user interface and data visualization components. RESULTS: We have designed the bioWidget toolkit as a set of JavaBean components. It includes a wide array of user interface components and defines an architecture for assembling applications. The toolkit is founded on established software engineering design patterns and principles, including componentry, Model-View-Controller, factored models and schema neutrality. As a proof of concept, we have used the bioWidget toolkit to create three extendible applications: AnnotView, BlastView and AlignView.
Steve Fischer, Jonathan Crabtree, Brian P. Brunk, M. Gibson, G. Christian Overton
Bioinform.4