Demo Data from EDBT 2026 / reviewers in the wild / expert
Xueer Weng
dblp:423/1184
· DBLP profile ↗
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
protein function prediction |
1.0 | 1 | 2026 | Molecular-level protein semantic learning via structure-aware coarse-grained language modeling · Bioinform. 2026 |
Bioinformatics and computational biology › protein sequence analysis › protein sequence representation
protein language model |
1.0 | 1 | 2026 | Molecular-level protein semantic learning via structure-aware coarse-grained language modeling · Bioinform. 2026 |
Bioinformatics and computational biology › protein analysis › protein bioinformatics
protein representation learning |
1.0 | 1 | 2026 | Molecular-level protein semantic learning via structure-aware coarse-grained language modeling · Bioinform. 2026 |
Methods — techniques the papers use, named apart from their topics
transformer · 1.0doc2vec · 1.0BERT · 1.0
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2026 | Molecular-level protein semantic learning via structure-aware coarse-grained language modelingabstractMOTIVATION: Protein language models (PLMs) have emerged as pivotal tools for protein representation, enabling significant advances in structure-function prediction and computational biology. However, current PLMs predominantly rely on fine-grained amino acid sequences as input, treating individual residues as tokens. While this approach facilitates semantic learning at the residue level, it struggles to capture molecular-level semantics, particularly for large proteins, where sequence truncation and inefficient local pattern extraction hinder holistic understanding. The spatial structure of a protein determines its function. Despite the critical role of protein function analysis, coarse-grained protein language frameworks that bridge sequence and structural semantics remain underdeveloped. RESULTS: To fill this gap, we introduce a novel structure-aware coarse-grained protein language that discretizes proteins into local structural patterns derived from their secondary structures. By constructing a vocabulary of these patterns as "words," we represent proteins as compact, structure-aware "sentences" significantly shorter than raw amino acid sequences. We benchmark the proposed coarse-grained language against three state-of-the-art fine-grained protein languages and a classical language modeling method in natural language processing, using two architectures: a lightweight Doc2Vec model and a Transformer-based BERT model, and evaluating performance across diverse downstream tasks, including function prediction, enzyme classification, and interaction identification. The proposed method achieves stable performance across three tasks, especially for long proteins. These results demonstrate that the proposed coarse-grained protein language preserves critical structural and functional semantics and improves molecular-level analysis, offering a promising direction for decoding higher-order biological insights. AVAILABILITY AND IMPLEMENTATION: The data and source code of the proposed method are available at GitHub (https://github.com/bug-0x3f/coarse-grained-protein-language) and Zenodo (DOI: 10.5281/zenodo.17674298). Jun Zhang 0078, Xueer Weng, Zexuan Zhu 0001 |
Bioinform. | 2 |