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Maria José Aranzana

dblp:370/1633 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2024
0000-0002-0240-8021ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 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
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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological data visualization
pedigree visualization
0.812024
PERSEUS: an interactive and intuitive web-based tool for pedigree visualization · Bioinform. 2024
Visualization and visual analytics
graph visualization
0.212024
PERSEUS: an interactive and intuitive web-based tool for pedigree visualization · Bioinform. 2024
Bioinformatics and computational biology › genomics
genotyping
0.212015
ASSIsT: an automatic SNP scoring tool for in- and outbreeding species · Bioinform. 2015
Bioinformatics and computational biology › genomics › computational genomics
SNP detection
0.212015
ASSIsT: an automatic SNP scoring tool for in- and outbreeding species · Bioinform. 2015
Bioinformatics and computational biology › statistical genetics
genetic mapping
0.112015
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
YearPublicationVenuePosition
2024 PERSEUS: an interactive and intuitive web-based tool for pedigree visualization
abstract
SUMMARY: 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.5
2015 ASSIsT: an automatic SNP scoring tool for in- and outbreeding species
abstract
UNLABELLED: 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.7