Demo Data from EDBT 2026 / reviewers in the wild / expert
Linda Payet
dblp:25/7068
· DBLP profile ↗
1ranked-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 · 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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › structural bioinformatics
nucleic acid structure analysis |
0.1 | 1 | 2009 | Predicting and understanding the stability of G-quadruplexes · Bioinform. 2009 |
Bioinformatics and computational biology
genomics |
0.0 | 1 | 2009 | Predicting and understanding the stability of G-quadruplexes · Bioinform. 2009 |
Methods — techniques the papers use, named apart from their topics
gaussian process regression · 0.1bayesian inference · 0.1active learning · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2009 | Predicting and understanding the stability of G-quadruplexesabstractMOTIVATION: G-quadruplexes are stable four-stranded guanine-rich structures that can form in DNA and RNA. They are an important component of human telomeres and play a role in the regulation of transcription and translation. The biological significance of a G-quadruplex is crucially linked with its thermodynamic stability. Hence the prediction of G-quadruplex stability is of vital interest. RESULTS: In this article, we present a novel Bayesian prediction framework based on Gaussian process regression to determine the thermodynamic stability of previously unmeasured G-quadruplexes from the sequence information alone. We benchmark our approach on a large G-quadruplex dataset and compare our method to alternative approaches. Furthermore, we propose an active learning procedure which can be used to iteratively acquire data in an optimal fashion. Lastly, we demonstrate the usefulness of our procedure on a genome-wide study of quadruplexes in the human genome. AVAILABILITY: A data table with the training sequences is available as supplementary material. Source code is available online at http://www.inference.phy.cam.ac.uk/os252/projects/quadruplexes. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oliver Stegle, Linda Payet, Jean-Louis Mergny, David J. C. MacKay, Julian Leon Huppert |
Bioinform. | 2 |