Jessica Hurt

dblp:434/1891 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2026
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 1 · 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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › transcriptomics
RNA splicing analysis
1.012026
SpliceHarmonization: an integrated method for identifying RNA splicing events in therapeutics for splicing modulation · Bioinform. 2026
Bioinformatics and computational biology › transcriptomics › RNA splicing analysis
splice variant prediction
1.012026
SpliceHarmonization: an integrated method for identifying RNA splicing events in therapeutics for splicing modulation · Bioinform. 2026
Bioinformatics and computational biology
transcriptomics
1.012026
SpliceHarmonization: an integrated method for identifying RNA splicing events in therapeutics for splicing modulation · Bioinform. 2026

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

ensemble integration · 1.0
YearPublicationVenuePosition
2026 SpliceHarmonization: an integrated method for identifying RNA splicing events in therapeutics for splicing modulation
abstract
MOTIVATION: Splicing, a critical co-transcriptional process in eukaryotes, enhances transcriptome diversity by generating isoforms specific to cell types, tissues, or developmental stages. Recent advancements in splicing modulators have opened new avenues for targeting previously undruggable genes by inducing significant perturbations in splicing events. These developments underscore the need for comprehensive methods to accurately identify and compare splicing events. While several tools have been developed to detect local splice variants, inconsistencies across methods remain a significant challenge. To address this, we present SpliceHarmonization, an integrated approach that combines the strengths of rMATS, LeafCutter, and MAJIQ, enabling robust and reliable splicing analysis with event type annotations. RESULTS: In a comprehensive evaluation using diverse simulated datasets, SpliceHarmonization streamlined and standardized the outputs from three detection methods into a unified format, thereby improving splicing detection with event type annotation and outperforming individual methods. By integrating the outputs from rMATS, LeafCutter, and MAJIQ, our approach not only enhanced identification of a wide range of splicing events but also effectively mitigated method-specific discrepancies. This integration led to an accuracy exceeding 0.8 and a recall of up to 0.5, with an observed increase in AUC of up to 10%. Furthermore, SpliceHarmonization demonstrated high sensitivity in detecting low-abundance and complex splicing events, providing annotations including genomic coordinates and event type. AVAILABILITY AND IMPLEMENTATION: SpliceHarmonization is available at https://github.com/interactivereport/SpliceHarmonization.
Yirui Chen, Yu H. Sun, Soumya Negi, Shaolong Cao, Zhengyu Ouyang, Baohong Zhang, Jessica Hurt, Dann Huh
Bioinform.8