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Brian Osborne

dblp:48/5381 · DBLP profile ↗
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3ranked-venue papers
0as first author
0since 2021 · last 2009
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2Artificial intelligence and machine learning · 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%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genome annotation › prokaryotic genome annotation
bacterial genome annotation
0.112009
DIYA: a bacterial annotation pipeline for any genomics lab · Bioinform. 2009
Bioinformatics and computational biology
genomics
0.112009
DIYA: a bacterial annotation pipeline for any genomics lab · Bioinform. 2009

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

modular pipeline · 0.1
YearPublicationVenuePosition
2009 DIYA: a bacterial annotation pipeline for any genomics lab
abstract
UNLABELLED: DIYA (Do-It-Yourself Annotator) is a modular and configurable open source pipeline software, written in Perl, used for the rapid annotation of bacterial genome sequences. The software is currently used to take DNA contigs as input, either in the form of complete genomes or the result of shotgun sequencing, and produce an annotated sequence in Genbank file format as output. AVAILABILITY: Distribution and source code are available at (https://sourceforge.net/projects/diyg/). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Andrew C. Stewart, Brian Osborne, Timothy D. Read
Bioinform.2
2007 Thickness measurement and crease detection of wheat grains using stereo vision
Changming Sun, Mark Berman 0002, David Coward, Brian Osborne
Pattern Recognit. Lett.4
2006 Gene functional similarity search tool (GFSST)
abstract
BACKGROUND: With the completion of the genome sequences of human, mouse, and other species and the advent of high throughput functional genomic research technologies such as biomicroarray chips, more and more genes and their products have been discovered and their functions have begun to be understood. Increasing amounts of data about genes, gene products and their functions have been stored in databases. To facilitate selection of candidate genes for gene-disease research, genetic association studies, biomarker and drug target selection, and animal models of human diseases, it is essential to have search engines that can retrieve genes by their functions from proteome databases. In recent years, the development of Gene Ontology (GO) has established structured, controlled vocabularies describing gene functions, which makes it possible to develop novel tools to search genes by functional similarity. RESULTS: By using a statistical model to measure the functional similarity of genes based on the Gene Ontology directed acyclic graph, we developed a novel Gene Functional Similarity Search Tool (GFSST) to identify genes with related functions from annotated proteome databases. This search engine lets users design their search targets by gene functions. CONCLUSION: An implementation of GFSST which works on the UniProt (Universal Protein Resource) for the human and mouse proteomes is available at GFSST Web Server. GFSST provides functions not only for similar gene retrieval but also for gene search by one or more GO terms. This represents a powerful new approach for selecting similar genes and gene products from proteome databases according to their functions.
Peisen Zhang, Huitao Sheng, James J. Russo, Brian Osborne, Kenneth H. Buetow
BMC Bioinform.5