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Euxhen Hasanaj

dblp:362/1389 · DBLP profile ↗
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2ranked-venue papers
2as first author
2since 2021 · last 2025
0000-0002-6940-8683ORCID · verified

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 · 92% Medical and health informatics · 8%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological network › network biology › network inference
gene regulatory network inference
0.912025
Recovering time-varying networks from single-cell data · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis
trajectory inference
0.812024
Integrating patients in time series clinical transcriptomics data · Bioinform. 2024
Bioinformatics and computational biology
transcriptomics
0.812024
Integrating patients in time series clinical transcriptomics data · Bioinform. 2024
Bioinformatics and computational biology › single-cell analysis
single-cell transcriptomics
0.312025
Recovering time-varying networks from single-cell data · Bioinform. 2025
Medical and health informatics › precision medicine
disease subtype discovery
0.212024
Integrating patients in time series clinical transcriptomics data · Bioinform. 2024

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

self-attention · 0.9recurrent neural network · 0.9meta-learning · 0.9deep neural network · 0.9multi-commodity flow · 0.8
YearPublicationVenuePosition
2025 Recovering time-varying networks from single-cell data
abstract
MOTIVATION: Gene regulation is a dynamic process that underlies all aspects of human development, disease response, and other biological processes. The reconstruction of temporal gene regulatory networks has conventionally relied on regression analysis, graphical models, or other types of relevance networks. With the large increase in time series single-cell data, new approaches are needed to address the unique scale and nature of these data for reconstructing such networks. RESULTS: Here, we develop a deep neural network, Marlene, to infer dynamic graphs from time series single-cell gene expression data. Marlene constructs directed gene networks using a self-attention mechanism where the weights evolve over time using recurrent units. By employing meta learning, the model is able to recover accurate temporal networks even for rare cell types. In addition, Marlene can identify gene interactions relevant to specific biological responses, including COVID-19 immune response, fibrosis, and aging, paving the way for potential treatments. AVAILABILITY AND IMPLEMENTATION: The code used to train Marlene is available at https://github.com/euxhenh/Marlene.
Euxhen Hasanaj, Barnabás Póczos, Ziv Bar-Joseph
Bioinform.1
2024 Integrating patients in time series clinical transcriptomics data
abstract
MOTIVATION: Analysis of time series transcriptomics data from clinical trials is challenging. Such studies usually profile very few time points from several individuals with varying response patterns and dynamics. Current methods for these datasets are mainly based on linear, global orderings using visit times which do not account for the varying response rates and subgroups within a patient cohort. RESULTS: We developed a new method that utilizes multi-commodity flow algorithms for trajectory inference in large scale clinical studies. Recovered trajectories satisfy individual-based timing restrictions while integrating data from multiple patients. Testing the method on multiple drug datasets demonstrated an improved performance compared to prior approaches suggested for this task, while identifying novel disease subtypes that correspond to heterogeneous patient response patterns. AVAILABILITY AND IMPLEMENTATION: The source code and instructions to download the data have been deposited on GitHub at https://github.com/euxhenh/Truffle.
Euxhen Hasanaj, Sachin Mathur, Ziv Bar-Joseph
Bioinform.1