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David Brett

dblp:33/6552 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2003
—ORCID · none

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%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genome annotation
annotation quality assessment
0.012003
Evaluation of annotation strategies using an entire genome sequence · Bioinform. 2003
Bioinformatics and computational biology › genome annotation
functional annotation
0.012003
Evaluation of annotation strategies using an entire genome sequence · Bioinform. 2003
Bioinformatics and computational biology
genome annotation
0.012003
Evaluation of annotation strategies using an entire genome sequence · Bioinform. 2003
Bioinformatics and computational biology › genome annotation
automatic annotation
0.012003
Evaluation of annotation strategies using an entire genome sequence · Bioinform. 2003

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

comparative analysis · 0.0
YearPublicationVenuePosition
2003 Evaluation of annotation strategies using an entire genome sequence
abstract
Abstract Motivation: Genome-wide functional annotation either by manual or automatic means has raised considerable concerns regarding the accuracy of assignments and the reproducibility of methodologies. In addition, a performance evaluation of automated systems that attempt to tackle sequence analyses rapidly and reproducibly is generally missing. In order to quantify the accuracy and reproducibility of function assignments on a genome-wide scale, we have re-annotated the entire genome sequence of Chlamydia trachomatis (serovar D), in a collaborative manner. Results: We have encoded all annotations in a structured format to allow further comparison and data exchange and have used a scale that records the different levels of potential annotation errors according to their propensity to propagate in the database due to transitive function assignments. We conclude that genome annotation may entail a considerable amount of errors, ranging from simple typographical errors to complex sequence analysis problems. The most surprising result of this comparative study is that automatic systems might perform as well as the teams of experts annotating genome sequences. Availability and supplementary information: http://www.ebi.ac.uk/research/cgg/annotation/cteval/ Contact: [email protected] * To whom correspondence should be addressed. † INA-EKETA, GR-57001 Thessaloniki, Greece ‡ Computational Biology Center, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA § Aetion Technologies LLC, Worthington, OH 43085, USA ¶ Institut Curie, F-75248 Paris, France ∥ CNRS, UMR6543, F-06108 Nice, France ** Alma Bioinformatics, E-28760 Madrid, Spain †† Cap Gemini Ernst & Young, London SW1X 7LX, UK ‡‡ Univ. of Rome ‘La Sapienza’, I-00185 Rome, Italy §§ MWG-Biotech AG, Ebersberg, D-85560 Berlin, Germany ¶¶ Wellcome Trust Biocentre, Univ. of Dundee, Dundee DD1 5HN, UK
Sophia Tsoka, Miguel A. Andrade-Navarro, Anton J. Enright, Mark Carroll, Patrick Poullet, Vasilis J. Promponas, Theodore Liakopoulos, Giorgos Palaios, Claude Pasquier, Stavros J. Hamodrakas, Javier Tamames, Asutosh T. Yagnik, Anna Tramontano, Damien Devos, Christian Blaschke, Alfonso Valencia, David Brett, David M. A. Martin, Christophe Leroy, Isidore Rigoutsos, Chris Sander, Christos A. Ouzounis
Bioinform.18