Demo Data from EDBT 2026 / reviewers in the wild / expert
Xianhai Li
dblp:276/0740
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2020
—ORCID · unresolved
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 · 87% Computational science and engineering · 13% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
epigenetics |
0.4 | 1 | 2020 | DNA4mC-LIP: a linear integration method to identify N4-methylcytosine site in multiple species · Bioinform. 2020 |
Bioinformatics and computational biology › proteomics › post-translational modification site prediction
n4-methylcytosine site prediction |
0.4 | 1 | 2020 | DNA4mC-LIP: a linear integration method to identify N4-methylcytosine site in multiple species · Bioinform. 2020 |
Computational science and engineering › ensemble learning
ensemble prediction |
0.1 | 1 | 2020 | DNA4mC-LIP: a linear integration method to identify N4-methylcytosine site in multiple species · Bioinform. 2020 |
Methods — techniques the papers use, named apart from their topics
machine learning · 0.4linear integration · 0.4
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | DNA4mC-LIP: a linear integration method to identify N4-methylcytosine site in multiple speciesabstractMOTIVATION: DNA N4-methylcytosine (4mC) is a crucial epigenetic modification. However, the knowledge about its biological functions is limited. Effective and accurate identification of 4mC sites will be helpful to reveal its biological functions and mechanisms. Since experimental methods are cost and ineffective, a number of machine learning-based approaches have been proposed to detect 4mC sites. Although these methods yielded acceptable accuracy, there is still room for the improvement of the prediction performance and the stability of existing methods in practical applications. RESULTS: In this work, we first systematically assessed the existing methods based on an independent dataset. And then, we proposed DNA4mC-LIP, a linear integration method by combining existing predictors to identify 4mC sites in multiple species. The results obtained from independent dataset demonstrated that DNA4mC-LIP outperformed existing methods for identifying 4mC sites. To facilitate the scientific community, a web server for DNA4mC-LIP was developed. We anticipated that DNA4mC-LIP could serve as a powerful computational technique for identifying 4mC sites and facilitate the interpretation of 4mC mechanism. AVAILABILITY AND IMPLEMENTATION: http://i.uestc.edu.cn/DNA4mC-LIP/. CONTACT: [email protected] or [email protected] or [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Qiang Tang 0013, Juanjuan Kang, Jiaqing Yuan, Hua Tang, Xianhai Li, Hao Lin 0001, Jian Huang 0004, Wei Chen 0064 |
Bioinform. | 5 |