Demo Data from VLDB 2026 / reviewers in the wild / expert
Denise Kalos
dblp:316/4483
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2022
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 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 2 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
biomarker discovery |
0.6 | 1 | 2022 | Efficient gradient boosting for prognostic biomarker discovery · Bioinform. 2022 |
Bioinformatics and computational biology › biomarker discovery
prognostic biomarker identification |
0.6 | 1 | 2022 | Efficient gradient boosting for prognostic biomarker discovery · Bioinform. 2022 |
Methods — techniques the papers use, named apart from their topics
light gradient boosting · 0.6gradient boosting decision tree · 0.6extreme gradient boosting · 0.6cox regression · 0.6
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2022 | Efficient gradient boosting for prognostic biomarker discoveryabstractMOTIVATION: A gradient boosting decision tree (GBDT) is a powerful ensemble machine-learning method that has the potential to accelerate biomarker discovery from high-dimensional molecular data. Recent algorithmic advances, such as extreme gradient boosting (XGB) and light gradient boosting (LGB), have rendered the GBDT training more efficient, scalable and accurate. However, these modern techniques have not yet been widely adopted in discovering biomarkers for censored survival outcomes, which are key clinical outcomes or endpoints in cancer studies. RESULTS: In this paper, we present a new R package 'Xsurv' as an integrated solution that applies two modern GBDT training frameworks namely, XGB and LGB, for the modeling of right-censored survival outcomes. Based on our simulations, we benchmark the new approaches against traditional methods including the stepwise Cox regression model and the original gradient boosting function implemented in the package 'gbm'. We also demonstrate the application of Xsurv in analyzing a melanoma methylation dataset. Together, these results suggest that Xsurv is a useful and computationally viable tool for screening a large number of prognostic candidate biomarkers, which may facilitate future translational and clinical research. AVAILABILITY AND IMPLEMENTATION: 'Xsurv' is freely available as an R package at: https://github.com/topycyao/Xsurv. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Kaiqiao Li, Sijie Yao, Biwei Cao, Denise Kalos, Pei Fen Kuan, Ruoqing Zhu |
Bioinform. | 6 |