Demo Data from VLDB 2026 / reviewers in the wild / expert
Cédric Lood
dblp:321/4584
· DBLP profile ↗
2ranked-venue papers
1as first author
2since 2021 · last 2025
0000-0001-7826-3378ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 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
2 papers |
Bioinformatics and computational biology · 100% |
Topics — the 6 heaviest of 7, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › network bioinformatics › biological network analysis
network analysis |
0.9 | 1 | 2025 | AFragmenter: schema-free, tuneable protein domain segmentation for AlphaFold protein structures · Bioinform. 2025 |
Bioinformatics and computational biology › protein structure analysis › protein domain identification
protein domain parsing |
0.9 | 1 | 2025 | AFragmenter: schema-free, tuneable protein domain segmentation for AlphaFold protein structures · Bioinform. 2025 |
Bioinformatics and computational biology
structural bioinformatics |
0.9 | 1 | 2025 | AFragmenter: schema-free, tuneable protein domain segmentation for AlphaFold protein structures · Bioinform. 2025 |
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly
assembly quality assessment |
0.6 | 1 | 2022 | SASpector: analysis of missing genomic regions in draft genomes of prokaryotes · Bioinform. 2022 |
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly |
0.6 | 1 | 2022 | SASpector: analysis of missing genomic regions in draft genomes of prokaryotes · Bioinform. 2022 |
Bioinformatics and computational biology
genomics |
0.6 | 1 | 2022 | SASpector: analysis of missing genomic regions in draft genomes of prokaryotes · Bioinform. 2022 |
Methods — techniques the papers use, named apart from their topics
predicted aligned error · 0.9leiden clustering · 0.9short-read assembly comparison · 0.6
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | AFragmenter: schema-free, tuneable protein domain segmentation for AlphaFold protein structuresabstractSUMMARY: Protein domain segmentation is a crucial aspect of understanding protein functions and interactions, and it is vital for protein modelling exercises and evolutionary studies. Current segmentation methods often rely on predefined classification schemes, leading to inconsistencies and biases. AFragmenter provides a schema-free and tuneable approach to protein domain segmentation based on network analysis of AlphaFold-predicted structures. Utilizing Predicted Aligned Error values, AFragmenter constructs a fully connected network of protein residues and identifies distinct structural domains by using Leiden clustering. This method empowers users to adjust parameters including contrast threshold and resolution, providing control over the segmentation process. AVAILABILITY AND IMPLEMENTATION: AFragmenter is implemented in Python3 and freely available under an MIT license. It can be found as a Python library and command line tool at https://github.com/sverwimp/AFragmenter, pip, and Conda. Stefaan Verwimp, Rob Lavigne, Cédric Lood, Vera van Noort |
Bioinform. | 3 |
| 2022 | SASpector: analysis of missing genomic regions in draft genomes of prokaryotesabstractSUMMARY: Missing regions in short-read assemblies of prokaryote genomes are often attributed to biases in sequencing technologies and to repetitive elements, the former resulting in low sequencing coverage of certain loci and the latter to unresolved loops in the de novo assembly graph. We developed SASpector, a command-line tool that compares short-read assemblies (draft genomes) to their corresponding closed assemblies and extracts missing regions to analyze them at the sequence and functional level. SASpector allows to benchmark the need for resolved genomes, can be integrated into pipelines to control the quality of assemblies, and could be used for comparative investigations of missingness in assemblies for which both short-read and long-read data are available in the public databases. AVAILABILITY AND IMPLEMENTATION: SASpector is available at https://github.com/LoGT-KULeuven/SASpector. The tool is implemented in Python3 and available through pip and Docker (0mician/saspector). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Cédric Lood, Alejandro Correa Rojo, Deniz Sinar, Emma Verkinderen, Rob Lavigne, Vera van Noort |
Bioinform. | 1 |