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Lewis Moffat

dblp:305/5703 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0002-9378-1250ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein sequence analysis
protein sequence modeling
0.512021
Increasing the accuracy of single sequence prediction methods using a deep semi-supervised learning framework · Bioinform. 2021
Bioinformatics and computational biology
protein structure prediction
0.512021
Increasing the accuracy of single sequence prediction methods using a deep semi-supervised learning framework · Bioinform. 2021
Bioinformatics and computational biology › protein structure prediction
secondary structure prediction
0.512021
Increasing the accuracy of single sequence prediction methods using a deep semi-supervised learning framework · Bioinform. 2021

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

semi-supervised learning · 0.5deep learning · 0.5
YearPublicationVenuePosition
2021 Increasing the accuracy of single sequence prediction methods using a deep semi-supervised learning framework
abstract
MOTIVATION: Over the past 50 years, our ability to model protein sequences with evolutionary information has progressed in leaps and bounds. However, even with the latest deep learning methods, the modelling of a critically important class of proteins, single orphan sequences, remains unsolved. RESULTS: By taking a bioinformatics approach to semi-supervised machine learning, we develop Profile Augmentation of Single Sequences (PASS), a simple but powerful framework for building accurate single-sequence methods. To demonstrate the effectiveness of PASS we apply it to the mature field of secondary structure prediction. In doing so we develop S4PRED, the successor to the open-source PSIPRED-Single method, which achieves an unprecedented Q3 score of 75.3% on the standard CB513 test. PASS provides a blueprint for the development of a new generation of predictive methods, advancing our ability to model individual protein sequences. AVAILABILITY AND IMPLEMENTATION: The S4PRED model is available as open source software on the PSIPRED GitHub repository (https://github.com/psipred/s4pred), along with documentation. It will also be provided as a part of the PSIPRED web service (http://bioinf.cs.ucl.ac.uk/psipred/). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Lewis Moffat, David T. Jones
Bioinform.1