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Ketrin Gjoni

dblp:425/3619 · DBLP profile ↗
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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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis
genomic sequence analysis
0.812024
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
0.812024
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
0.812024
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
0.812024
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
YearPublicationVenuePosition
2024 SuPreMo: a computational tool for streamlining in silico perturbation using sequence-based predictive models
abstract
SUMMARY: 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