IDEPI
IDEPI predicts HIV-1 phenotypic traits from viral sequence data to identify genotype-to-phenotype relationships relevant to antibody neutralization, coreceptor tropism, compartmentalization, and drug-resistance mutations.
Key Features:
- Machine Learning Platform: Uses open-source general-purpose machine learning algorithms and libraries to build predictive models correlating genotypes with phenotypes.
- Phenotype Prediction: Applies trained models to classify sequences with unknown phenotypes and predict traits such as susceptibility to neutralization by specific antibodies.
- Feature Identification: Identifies specific sequence features that contribute to phenotypic outcomes, enabling interpretation of genetic determinants.
- Implementation: Provided as cross-platform Python source code for computational use.
Scientific Applications:
- Epitope Prediction for Broadly Neutralizing Antibodies (bNab): Identifies epitopes recognized by broadly neutralizing antibodies to inform vaccine-related studies.
- Coreceptor Tropism Determination: Predicts HIV-1 coreceptor usage to inform studies of viral entry and pathogenesis.
- Compartment-Specific Genetic Signatures: Detects genetic signatures specific to host compartments to study viral compartmentalization.
- Drug-Resistance Mutation Deduction: Deduces mutations associated with drug resistance to inform treatment-relevant analyses.
Methodology:
IDEPI trains machine learning models on sequence data with known phenotypes to learn genotype-to-phenotype relationships and then applies these models to new sequences to predict phenotypes and identify contributing genetic elements.
Topics
Details
- License:
- GPL-3.0
- Tool Type:
- library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Python
- Added:
- 5/1/2018
- Last Updated:
- 12/10/2018
Operations
Publications
Hepler NL, Scheffler K, Weaver S, Murrell B, Richman DD, Burton DR, Poignard P, Smith DM, Kosakovsky Pond SL. IDEPI: Rapid Prediction of HIV-1 Antibody Epitopes and Other Phenotypic Features from Sequence Data Using a Flexible Machine Learning Platform. PLoS Computational Biology. 2014;10(9):e1003842. doi:10.1371/journal.pcbi.1003842. PMID:25254639. PMCID:PMC4177671.