Detailed Information on Publication Record
2021
Intrinsic-Extrinsic Convolution and Pooling for Learning on 3D Protein Structures
HERMOSILLA CASAJÚS, Pedro, Marco SCHÄFER, Matěj LANG, Gloria FACKELMANN, Pere-Pau VÁZQUEZ ALCOCER et. al.Basic information
Original name
Intrinsic-Extrinsic Convolution and Pooling for Learning on 3D Protein Structures
Authors
HERMOSILLA CASAJÚS, Pedro (724 Spain), Marco SCHÄFER (276 Germany), Matěj LANG (203 Czech Republic, belonging to the institution), Gloria FACKELMANN (276 Germany), Pere-Pau VÁZQUEZ ALCOCER (724 Spain), Barbora KOZLÍKOVÁ (203 Czech Republic, belonging to the institution), Michael KRONE (276 Germany), Tobias RITSCHEL (276 Germany) and Timo ROPINSKI
Edition
International Conference on Learning Representations (ICLR), 2021
Other information
Language
English
Type of outcome
Prezentace na konferencích
Field of Study
10200 1.2 Computer and information sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
RIV identification code
RIV/00216224:14330/21:00118838
Organization unit
Faculty of Informatics
Keywords in English
classification; bioinformatics
Tags
International impact, Reviewed
Změněno: 15/5/2024 02:25, RNDr. Pavel Šmerk, Ph.D.
Abstract
V originále
The result is a paper (16 pages) at International Conference on Learning Representations. Although it is among the very best conferences in CS, since its proceedings do not have an ISBN or ISSN, the result cannot be transferred to the RIV database as a result of type D. The original abstract follows: Proteins perform a large variety of functions in living organisms and thus play a key role in biology. However, commonly used algorithms in protein learning were not specifically designed for protein data, and are therefore not able to capture all relevant structural levels of a protein during learning. To fill this gap, we propose two new learning operators, specifically designed to process protein structures. First, we introduce a novel convolution operator that considers the primary, secondary, and tertiary structure of a protein by using n-D convolutions defined on both the Euclidean distance, as well as multiple geodesic distances between the atoms in a multi-graph. Second, we introduce a set of hierarchical pooling operators that enable multi-scale protein analysis. We further evaluate the accuracy of our algorithms on common downstream tasks, where we outperform state-of-the-art protein learning algorithms.
Links
GC18-18647J, research and development project |
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