Demo Data from EDBT 2026 / reviewers in the wild / expert
Saleh Riahi
dblp:151/3470
· DBLP profile ↗
2ranked-venue papers
1as first author
2since 2021 · last 2024
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 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 · 73% Medical and health informatics · 27% |
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 › drug discovery
computational drug discovery |
0.8 | 1 | 2024 | Representations of lipid nanoparticles using large language models for transfection efficiency prediction · Bioinform. 2024 |
Medical and health informatics
drug delivery |
0.8 | 1 | 2024 | Representations of lipid nanoparticles using large language models for transfection efficiency prediction · Bioinform. 2024 |
Bioinformatics and computational biology
protein function prediction |
0.7 | 1 | 2023 | Surface ID: a geometry-aware system for protein molecular surface comparison · Bioinform. 2023 |
Bioinformatics and computational biology
structural bioinformatics |
0.7 | 1 | 2023 | Surface ID: a geometry-aware system for protein molecular surface comparison · Bioinform. 2023 |
Methods — techniques the papers use, named apart from their topics
large language model embeddings · 0.8gradient boosting · 0.8surface alignment · 0.7geometric deep learning · 0.7clustering · 0.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Representations of lipid nanoparticles using large language models for transfection efficiency predictionabstractMOTIVATION: Lipid nanoparticles (LNPs) are the most widely used vehicles for mRNA vaccine delivery. The structure of the lipids composing the LNPs can have a major impact on the effectiveness of the mRNA payload. Several properties should be optimized to improve delivery and expression including biodegradability, synthetic accessibility, and transfection efficiency. RESULTS: To optimize LNPs, we developed and tested models that enable the virtual screening of LNPs with high transfection efficiency. Our best method uses the lipid Simplified Molecular-Input Line-Entry System (SMILES) as inputs to a large language model. Large language model-generated embeddings are then used by a downstream gradient-boosting classifier. As we show, our method can more accurately predict lipid properties, which could lead to higher efficiency and reduced experimental time and costs. AVAILABILITY AND IMPLEMENTATION: Code and data links available at: https://github.com/Sanofi-Public/LipoBART. Saeed Moayedpour, Jonathan Broadbent, Saleh Riahi, Michael Bailey, Hoa V. Thu, Dimitar A. Dobchev, Akshay Balsubramani, Ricardo N. D. Santos, Lorenzo Kogler-Anele, Alejandro Corrochano-Navarro, Sizhen Li, Fernando U. Montoya, Vikram Agarwal, Ziv Bar-Joseph, Sven Jager |
Bioinform. | 3 |
| 2023 | Surface ID: a geometry-aware system for protein molecular surface comparisonabstractMOTIVATION: A protein can be represented in several forms, including its 1D sequence, 3D atom coordinates, and molecular surface. A protein surface contains rich structural and chemical features directly related to the protein's function such as its ability to interact with other molecules. While many methods have been developed for comparing the similarity of proteins using the sequence and structural representations, computational methods based on molecular surface representation are limited. RESULTS: Here, we describe "Surface ID," a geometric deep learning system for high-throughput surface comparison based on geometric and chemical features. Surface ID offers a novel grouping and alignment algorithm useful for clustering proteins by function, visualization, and in silico screening of potential binding partners to a target molecule. Our method demonstrates top performance in surface similarity assessment, indicating great potential for protein functional annotation, a major need in protein engineering and therapeutic design. AVAILABILITY AND IMPLEMENTATION: Source code for the Surface ID model, trained weights, and inference script are available at https://github.com/Sanofi-Public/LMR-SurfaceID. Saleh Riahi, Jae Hyeon Lee, Taylor Sorenson, Shuai Wei, Sven Jager, Reza Olfati-Saber, Yanfeng Zhou, Anna Park, Maria Wendt, Hervé Minoux |
Bioinform. | 1 |