Demo Data from VLDB 2026 / reviewers in the wild / expert
Ketrin Gjoni
dblp:425/3619
· DBLP profile ↗
1ranked-venue papers
1as first author
1since 2021 · last 2024
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › sequence analysis
genomic sequence analysis |
0.8 | 1 | 2024 | SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive models · Bioinform. 2024 |
Bioinformatics and computational biology › protein analysis › protein bioinformatics
in silico mutagenesis |
0.8 | 1 | 2024 | SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive models · Bioinform. 2024 |
Bioinformatics and computational biology › clinical bioinformatics
pathogenic variant prioritization |
0.8 | 1 | 2024 | SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive models · Bioinform. 2024 |
Bioinformatics and computational biology › statistical genetics
variant effect prediction |
0.8 | 1 | 2024 | SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive models · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
sequence-based machine learning · 0.83d genome disruption scoring · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive modelsabstractSUMMARY: The increasing development of sequence-based machine learning models has raised the demand for manipulating sequences for this application. However, existing approaches to edit and evaluate genome sequences using models have limitations, such as incompatibility with structural variants, challenges in identifying responsible sequence perturbations, and the need for vcf file inputs and phased data. To address these bottlenecks, we present Sequence Mutator for Predictive Models (SuPreMo), a scalable and comprehensive tool for performing and supporting in silico mutagenesis experiments. We then demonstrate how pairs of reference and perturbed sequences can be used with machine learning models to prioritize pathogenic variants or discover new functional sequences. AVAILABILITY AND IMPLEMENTATION: SuPreMo was written in Python, and can be run using only one line of code to generate both sequences and 3D genome disruption scores. The codebase, instructions for installation and use, and tutorials are on the GitHub page: https://github.com/ketringjoni/SuPreMo. Ketrin Gjoni, Katherine S. Pollard |
Bioinform. | 1 |