MultiCapsNet
MultiCapsNet performs integrative, interpretable classification of heterogeneous biological datasets by applying Capsule Network–based architectures (CapsNet, scCapsNet) to generate importance scores for data sources such as variant calls, single-cell RNA sequencing (scRNA-seq), protein-protein interactions (PPI), and protein-DNA interactions (PDI).
Key Features:
- Integration of Diverse Data Types: Integrates variant calls, scRNA-seq, PPI, and PDI across heterogeneous formats and lengths.
- Interpretable Classification: Generates direct importance scores for data sources to quantify each source's contribution to predictions without additional post hoc steps.
- Modular Input Handling: Processes modular features and PPI cluster nodes that are challenging for conventional interpretable methods such as linear regression or random forest.
Scientific Applications:
- Variant Call Classification: Classifies labeled variant call datasets with performance comparable to traditional neural networks while providing direct importance scores per data source.
- Single-Cell RNA Sequencing Analysis: Integrates scRNA-seq with PPI and PDI to classify cell types with accuracy comparable to neural networks and random forest and to identify roles of transcription factors (TFs) and PPI cluster nodes.
- Comparison with Existing Methods: Identified cell-type relevant TFs that were consistent with SCENIC in comparative analyses.
Methodology:
Built on Capsule Networks (CapsNet) and scCapsNet, the architecture captures spatial hierarchies in data and produces direct importance scores for input data sources to enable interpretable classification.
Topics
Details
- License:
- Not licensed
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python
- Added:
- 5/19/2022
- Last Updated:
- 5/19/2022
Operations
Publications
Wang L, Miao X, Nie R, Zhang Z, Zhang J, Cai J. MultiCapsNet: A General Framework for Data Integration and Interpretable Classification. Frontiers in Genetics. 2022;12. doi:10.3389/fgene.2021.767602. PMID:34899854. PMCID:PMC8652257.