Demo Data from VLDB 2026 / reviewers in the wild / expert
Céline Baldeyron
dblp:44/8712
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2010
0000-0003-2311-1523ORCID · reported
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 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › bioimage informatics › bioimage analysis › microscopy image analysis
cell segmentation and tracking |
0.1 | 1 | 2010 | Automated analysis of time-lapse fluorescence microscopy images: from live cell images to intracellular foci · Bioinform. 2010 |
Bioinformatics and computational biology › bioimage informatics › bioimage analysis › microscopy image analysis
fluorescence microscopy |
0.1 | 1 | 2010 | Automated analysis of time-lapse fluorescence microscopy images: from live cell images to intracellular foci · Bioinform. 2010 |
Bioinformatics and computational biology › bioimage informatics › bioimage analysis
microscopy image analysis |
0.1 | 1 | 2010 | Automated analysis of time-lapse fluorescence microscopy images: from live cell images to intracellular foci · Bioinform. 2010 |
Methods — techniques the papers use, named apart from their topics
pattern analysis · 0.1image segmentation · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2010 | Automated analysis of time-lapse fluorescence microscopy images: from live cell images to intracellular fociabstractMOTIVATION: Complete, accurate and reproducible analysis of intracellular foci from fluorescence microscopy image sequences of live cells requires full automation of all processing steps involved: cell segmentation and tracking followed by foci segmentation and pattern analysis. Integrated systems for this purpose are lacking. RESULTS: Extending our previous work in cell segmentation and tracking, we developed a new system for performing fully automated analysis of fluorescent foci in single cells. The system was validated by applying it to two common tasks: intracellular foci counting (in DNA damage repair experiments) and cell-phase identification based on foci pattern analysis (in DNA replication experiments). Experimental results show that the system performs comparably to expert human observers. Thus, it may replace tedious manual analyses for the considered tasks, and enables high-content screening. AVAILABILITY AND IMPLEMENTATION: The described system was implemented in MATLAB (The MathWorks, Inc., USA) and compiled to run within the MATLAB environment. The routines together with four sample datasets are available at http://celmia.bigr.nl/. The software is planned for public release, free of charge for non-commercial use, after publication of this article. Oleh Dzyubachyk, Jeroen Essers, Wiggert A. van Cappellen, Céline Baldeyron, Akiko Inagaki, Wiro J. Niessen, Erik Meijering |
Bioinform. | 4 |