AMPBenchmark
AMPBenchmark provides standardized, bias-aware benchmarking for antimicrobial peptide (AMP) prediction models to assess how negative data sampling strategies affect model performance.
Key Features:
- Comprehensive Model Evaluation: Evaluates 660 predictive models generated from 12 distinct machine learning architectures trained on a single positive dataset and tested using 11 distinct negative data sampling methods.
- Bias Quantification: Identifies and quantifies the influence of negative data sampling on benchmarking outcomes to reveal sampling-induced bias in model performance comparisons.
- Standardized Benchmarking Framework: Provides a standardized evaluation framework that holds positive data constant while varying negative sampling strategies to enable fair comparison of AMP prediction models.
Scientific Applications:
- Novel AMP Discovery: Supports comparative assessment of prediction models to prioritize candidate antimicrobial peptides for experimental validation.
- Drug Development: Informs selection of high-performing predictive models for prioritizing AMP candidates in antibiotic discovery workflows.
- Viral and Cancer Research: Enables evaluation and selection of models that predict AMPs with reported activity against viruses and cancer cells.
Methodology:
Performs systematic analysis of predictive models using a single consistent positive dataset while varying negative data sampling methods, evaluating 660 models produced from 12 machine learning architectures across 11 negative sampling strategies.
Topics
Details
- License:
- Not licensed
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- R
- Added:
- 1/20/2023
- Last Updated:
- 1/20/2023
Operations
Publications
Sidorczuk K, Gagat P, Pietluch F, Kała J, Rafacz D, Bąkała L, Słowik J, Kolenda R, Rödiger S, Fingerhut LCHW, Cooke IR, Mackiewicz P, Burdukiewicz M. Benchmarks in antimicrobial peptide prediction are biased due to the selection of negative data. Briefings in Bioinformatics. 2022;23(5). doi:10.1093/bib/bbac343. PMID:35988923. PMCID:PMC9487607.