EvoAug-TF

EvoAug-TF implements evolution-inspired data augmentation within TensorFlow to generate synthetic genomic sequences for training deep neural networks that predict molecular functions of non-coding genomic regions.


Key Features:

  • Evolution-Inspired Augmentation: Generates synthetic training sequences using evolution-inspired transformations to augment functional genomics datasets and improve model generalization.
  • TensorFlow Integration: Provides an implementation compatible with TensorFlow-based genomic deep learning architectures.
  • Performance Benchmarking: Includes systematic benchmarking that demonstrates performance comparable to the original EvoAug package.
  • Reproducibility Scripts: Supplies scripts to reproduce the reported benchmarking results.
  • Support for Interpretability: Augmentation is intended to facilitate development of interpretable models and attribution analysis for genomic regulatory mechanisms.

Scientific Applications:

  • Genomic DNN Training: Augments limited functional genomics datasets to enable training of deep neural networks for predicting molecular functions of non-coding regions.
  • Model Generalization: Improves model generalization across diverse biological contexts by increasing training data diversity.
  • Attribution and Regulatory Analysis: Supports attribution analysis to aid interpretation of learned sequence features and regulatory mechanisms.

Methodology:

Implements evolution-inspired data augmentation to generate synthetic training sequences within TensorFlow, performs systematic benchmarking against EvoAug, and provides scripts to reproduce benchmarking results.

Topics

Details

License:
MIT
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
6/17/2024
Last Updated:
11/24/2024

Operations

Publications

Yu Y, Muthukumar S, Koo PK. EvoAug-TF: extending evolution-inspired data augmentations for genomic deep learning to TensorFlow. Bioinformatics. 2024;40(3). doi:10.1093/bioinformatics/btae092. PMID:38366935. PMCID:PMC10918628.

PMID: 38366935
Funding: - National Institutes of Health: R01GM149921 - National Human Genome Research Institute of the National Institutes of Health: R01HG012131 - US National Institutes of Health: S10OD028632-01

Documentation