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Katalin Ferenc

dblp:378/4147 · DBLP profile ↗
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2ranked-venue papers
2as first author
2since 2021 · last 2026
0000-0002-3006-4297ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 2 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 · 57% Computing education · 43%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene regulation
regulatory genomics
1.012026
inMOTIFin: a lightweight end-to-end simulation software for regulatory sequences · Bioinform. 2026
Computing education › software engineering education
team-based software development
0.812024
Improving bioinformatics software quality through teamwork · Bioinform. 2024
Bioinformatics and computational biology › sequence analysis
motif discovery
0.312026
inMOTIFin: a lightweight end-to-end simulation software for regulatory sequences · Bioinform. 2026

Methods — techniques the papers use, named apart from their topics

simulation · 1.0
YearPublicationVenuePosition
2026 inMOTIFin: a lightweight end-to-end simulation software for regulatory sequences
abstract
SUMMARY: The accurate development, assessment, interpretation, and benchmarking of bioinformatics frameworks for analyzing transcriptional regulatory grammars rely on controlled simulations to validate the underlying methods. However, existing simulators often lack end-to-end flexibility or ease of integration, which limits their practical use. We present inMOTIFin, a lightweight, modular, and user-friendly Python-based software that addresses these gaps by providing versatile and efficient simulation and modification of DNA regulatory sequences. inMOTIFin enables users to simulate or modify regulatory sequences efficiently for the customizable generation of motifs and insertion of motif instances with precise control over their positions, co-occurrences, and spacing, as well as direct modification of real sequences, facilitating a comprehensive evaluation of motif-based methods and interpretation tools. We demonstrate inMOTIFin applications for the assessment of de novo motif discovery, the analysis of transcription factor cooperativity, and the support of explainability analyses for deep learning models. inMOTIFin ensures robust and reproducible analyses for studying transcriptional regulatory grammars. AVAILABILITY AND IMPLEMENTATION: inMOTIFin is available at PyPI https://pypi.org/project/inMOTIFin/ and Docker Hub https://hub.docker.com/r/cbgr/inmotifin. Detailed documentation is available at https://inmotifin.readthedocs.io/en/latest/. The code for use case analyses is available at https://bitbucket.org/CBGR/inmotifin_evaluation/src/main/. The version of the code used for this article has been uploaded to Zenodo with DOI: 10.5281/zenodo.17638579.
Katalin Ferenc, Lorenzo Martini, Ieva Rauluseviciute, Geir Kjetil Sandve, Anthony Mathelier
Bioinform.1
2024 Improving bioinformatics software quality through teamwork
abstract
SUMMARY: Since high-throughput techniques became a staple in biological science laboratories, computational algorithms, and scientific software have boomed. However, the development of bioinformatics software usually lacks software development quality standards. The resulting software code is hard to test, reuse, and maintain. We believe that the root of inefficiency in implementing the best software development practices in academic settings is the individualistic approach, which has traditionally been the norm for recognizing scientific achievements and, by extension, for developing specialized software. Software development is a collective effort in most software-heavy endeavors. Indeed, the literature suggests teamwork directly impacts code quality through knowledge sharing, collective software development, and established coding standards. In our computational biology research groups, we sustainably involve all group members in learning, sharing, and discussing software development while maintaining the personal ownership of research projects and related software products. We found that group members involved in this endeavor improved their coding skills, became more efficient bioinformaticians, and obtained detailed knowledge about their peers' work, triggering new collaborative projects. We strongly advocate for improving software development culture within bioinformatics through collective effort in computational biology groups or institutes with three or more bioinformaticians. AVAILABILITY AND IMPLEMENTATION: Additional information and guidance on how to get started is available at https://ferenckata.github.io/ImprovingSoftwareTogether.github.io/.
Katalin Ferenc, Ieva Rauluseviciute, Ladislav Hovan, Marieke L. Kuijjer, Anthony Mathelier
Bioinform.1