Evolutionarily informed deep learning methods for predicting relative transcript abundance from DNA sequence.
Jacob D WashburnMaria Katherine Mejia-GuerraGuillaume RamsteinKarl A KremlingRavi ValluruEdward S BucklerHai WangPublished in: Proceedings of the National Academy of Sciences of the United States of America (2019)
Deep learning methodologies have revolutionized prediction in many fields and show potential to do the same in molecular biology and genetics. However, applying these methods in their current forms ignores evolutionary dependencies within biological systems and can result in false positives and spurious conclusions. We developed two approaches that account for evolutionary relatedness in machine learning models: (i) gene-family-guided splitting and (ii) ortholog contrasts. The first approach accounts for evolution by constraining model training and testing sets to include different gene families. The second approach uses evolutionarily informed comparisons between orthologous genes to both control for and leverage evolutionary divergence during the training process. The two approaches were explored and validated within the context of mRNA expression level prediction and have the area under the ROC curve (auROC) values ranging from 0.75 to 0.94. Model weight inspections showed biologically interpretable patterns, resulting in the hypothesis that the 3' UTR is more important for fine-tuning mRNA abundance levels while the 5' UTR is more important for large-scale changes.
Keyphrases
- deep learning
- genome wide
- machine learning
- artificial intelligence
- dna methylation
- convolutional neural network
- copy number
- genome wide identification
- antibiotic resistance genes
- virtual reality
- physical activity
- single molecule
- air pollution
- rna seq
- circulating tumor
- weight loss
- cell free
- transcription factor
- human health
- amino acid
- wastewater treatment
- risk assessment