描述者:对比测试安全神经网络评估方法用于蛋白质序列分类 (iDASH24)
Arif Harmanci1, Luyao Chen1, Miran Kim2
1Department of Health Data Science and Artificial Intelligence, D. Bradley McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, TX 77030 USA.
概括
通过iDASH24数据集,可以对使用同态加密的基于变压器的模型进行安全评估的标准化测试和基准测试. 本资源有助于开发和评估对基因组数据的保护隐私的机器学习策略.
科学领域:
- 计算生物学是一种计算生物学.
- 密码学 密码学 密码学 密码学
- 机器学习 机器学习
背景情况:
- 变压器模型在生物信息学中越来越多地使用,这引发了对敏感基因组数据的隐私问题.
- 对这些模型的安全评估对于保护隐私的分析至关重要.
- 现有的安全模型评估基准有限.
研究的目的:
- 引入iDASH24同型加密轨道数据集,用于对变压器模型进行安全评估.
- 为测试保护隐私的机器学习技术提供标准化资源.
- 促进开发安全的基因组数据分析方法.
主要方法:
- 设计了一个包含蛋白质家族分类变压器模型和相关示例数据的数据集.
- 使用同态加密方案进行安全的模型评估.
- 组织了iDASH24基因组隐私竞赛,以测试安全评估策略.
主要成果:
- 在竞争环境中,iDASH24数据集已成功地用于对变压器模型的安全评估.
- 在竞赛期间生成了基准测试结果和伴随方法.
- 该数据集促进了对同型加密进行安全机器学习的探索.
结论:
- iDASH24数据集是对神经网络模型,特别是变压器的安全评估进行基准测试的宝贵资源.
- 它支持在基因组学中推进保护隐私的机器学习.
- 方便在AI中对同型加密应用程序进行标准化测试.
更多相关视频
09:34A Virtual Machine Platform for Non-Computer Professionals for Using Deep Learning to Classify Biological Sequences of Metagenomic Data
Published on: September 25, 2021
3.9K
08:31Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions
Published on: December 1, 2020
4.9K
相关概念视频
Protein Networks
3.9K
An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
3.9K
Protein-protein Interfaces
12.5K
Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
12.5K
Conserved Binding Sites
4.2K
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
4.2K
