Demo Data from EDBT 2026 / reviewers in the wild / expert
Pere Arús
dblp:172/0386
· DBLP profile ↗
3ranked-venue papers
0as first author
2since 2021 · last 2025
0000-0003-0939-8038ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 3 · 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% | |
| Computer graphics and multimedia
1 paper |
Visualization and visual analytics · 100% |
Topics — the 5 heaviest of 6, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › biological data visualization
pedigree visualization |
0.8 | 1 | 2024 | PERSEUS: an interactive and intuitive web-based tool for pedigree visualization · Bioinform. 2024 |
Visualization and visual analytics
graph visualization |
0.2 | 1 | 2024 | PERSEUS: an interactive and intuitive web-based tool for pedigree visualization · Bioinform. 2024 |
Bioinformatics and computational biology › genomics
genotyping |
0.2 | 1 | 2015 | ASSIsT: an automatic SNP scoring tool for in- and outbreeding species · Bioinform. 2015 |
Bioinformatics and computational biology › genomics › computational genomics
SNP detection |
0.2 | 1 | 2015 | ASSIsT: an automatic SNP scoring tool for in- and outbreeding species · Bioinform. 2015 |
Bioinformatics and computational biology › statistical genetics
genetic mapping |
0.1 | 1 | 2015 | ASSIsT: an automatic SNP scoring tool for in- and outbreeding species · Bioinform. 2015 |
Methods — techniques the papers use, named apart from their topics
force-directed graph layout · 1.5bi-allelic genetic model · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | ResynPy: a software for selecting pairs of complementary inbred lines to resynthesize valuable heterozygous genotypesabstractBACKGROUND: Using cultivars based on a single, partly heterozygous, genotype is one of the bases of agriculture, frequently used in seed-propagated species such as vegetables and field crops (F1 hybrid varieties), and in most fruit trees and ornamentals (clonal varieties) that reproduce vegetatively. Producing two inbred lines that fully or partly reconstruct a given high-value heterozygous individual is now possible with the Resynthesis method, which uses molecular markers to select pairs of complementary genotypes in the F2 and subsequent selfing generations. The objective of this paper was to develop a software to facilitate the selection of such complementary pairs from a large number of segregating genotyped individuals. RESULTS: The ResynPy tool we developed screens the genotyping data of a segregating population, originating from selfing a top-performing partly heterozygous individual, and detects pairs of individuals that could produce progeny containing individuals nearly identical to the initial elite genotype. Our software selects candidate pairs of individuals in a small timeframe window with a low memory footprint. ResynPy tool could be part of a breeding toolkit to accelerate breeding programs in any plant species of economic importance capable of producing self-pollinated progeny. CONCLUSIONS: ResynPy is a software developed in Python language and is freely available on GitHub (HYPERLINK " https://github.com/kostasgalexiou/ResynPy/tree/main "). ResynPy automates the process of individual selection implemented by the Resynthesis method, in a highly efficient manner through parallelization, allowing to plant breeders for detection of pairs of complementary individuals in a selfing population that could be suitable parents to a plant variety with economically important agronomic traits. With ResynPy, breeders are provided with a fast and easy-to-use tool that will aid them to advance their plant breeding programs. Konstantinos G. Alexiou, Iban Eduardo, Pere Arús |
BMC Bioinform. | 3 |
| 2024 | PERSEUS: an interactive and intuitive web-based tool for pedigree visualizationabstractSUMMARY: Pedigree-based analyses' prime role is to unravel relationships between individuals in breeding programs and germplasms. This is critical information for decoding the genetics underlying main inherited traits of relevance, and unlocking the genotypic variability of a species to carry out genomic selections and predictions. Despite the great interest, current lineage visualizations become quite limiting in terms of public display, exploration, and tracing of traits up to ancestral donors. PERSEUS is a user-friendly, intuitive, and interactive web-based tool for pedigree visualizations represented as directed graph networks distributed using a force-repulsion method. The visualizations do not only showcase individual relationships among accessions, but also facilitate a seamless search and download of phenotypic traits along the pedigrees. PERSEUS is a promising tool for breeders and scientists, advantageous for evolutionary, genealogy, and diversity analyses among related accessions and species. AVAILABILITY AND IMPLEMENTATION: PERSEUS is freely accessible at https://bioinformatics.cragenomica.es/perseus and GitHub code is available at https://github.com/aranzana-lab/PERSEUS. Nicole Pradas, Federico Jurado-Ruiz, Carles Onielfa, Pere Arús, Maria José Aranzana |
Bioinform. | 4 |
| 2015 | ASSIsT: an automatic SNP scoring tool for in- and outbreeding speciesabstractUNLABELLED: ASSIsT (Automatic SNP ScorIng Tool) is a user-friendly customized pipeline for efficient calling and filtering of SNPs from Illumina Infinium arrays, specifically devised for custom genotyping arrays. Illumina has developed an integrated software for SNP data visualization and inspection called GenomeStudio (GS). ASSIsT builds on GS-derived data and identifies those markers that follow a bi-allelic genetic model and show reliable genotype calls. Moreover, ASSIsT re-edits SNP calls with null alleles or additional SNPs in the probe annealing site. ASSIsT can be employed in the analysis of different population types such as full-sib families and mating schemes used in the plant kingdom (backcross, F1, F2), and unrelated individuals. The final result can be directly exported in the format required by the most common software for genetic mapping and marker-trait association analysis. ASSIsT is developed in Python and runs in Windows and Linux. AVAILABILITY AND IMPLEMENTATION: The software, example data sets and tutorials are freely available at http://compbiotoolbox.fmach.it/assist/. CONTACT: [email protected]. Mario Di Guardo, Diego Micheletti, Luca Bianco, Herma J. J. Koehorst-van Putten, Sara Longhi, Fabrizio Costa, Maria José Aranzana, Riccardo Velasco, Pere Arús, Michela Troggio, Eric W. van de Weg |
Bioinform. | 9 |