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Reaping the Fruits of LLM Pruning: Towards Small Language Models for Efficient Non-Coding Variant Effect Prediction
Megha Hegde1, Jean-Christophe Nebel2, Farzana Rahman1
1School of Computer Science and Mathematics, Kingston University, London KT1 2EE, UK.
Layer pruning makes large genomic language models more efficient for variant prediction. Removing redundant layers reduces computational demands without sacrificing accuracy, improving non-coding variant interpretation.
Area of Science:
- Genomics
- Computational Biology
- Artificial Intelligence
Background:
- Interpreting genetic variants is crucial for precision medicine.
- Large genomic language models (LLMs) struggle with non-coding variant prediction due to computational scaling.
- Layer pruning, successful in natural language processing, can optimize LLMs.
Purpose of the Study:
- To systematically evaluate the contribution of each Transformer layer in genomic LLMs (DNABERT 2, Nucleotide Transformer) for variant prediction.
- To develop pruned, more computationally efficient LLMs by removing non-critical layers.
- To assess the performance of pruned LLMs on a non-coding variant effect prediction benchmark.
Main Methods:
- Systematic layer ablation of DNABERT 2 and Nucleotide Transformer models.
- Building layer importance profiles based on performance changes.
- Fine-tuning pruned and full models on the Enformer eQTL causal variant dataset.
- Comparing performance metrics (accuracy, AUC) and resource usage (training time, memory).
Main Results:
- Layer importance varied significantly across models, with some layers being removable with minimal performance loss.
- Pruned models achieved accuracy and AUC comparable to full models after fine-tuning.
- Pruned models demonstrated substantial reductions in training time and memory requirements.
Conclusions:
- Layer-wise pruning is an effective strategy for creating compact and efficient genomic LLMs.
- Pruned LLMs maintain predictive power while significantly lowering computational demands.
- This approach enhances the accessibility of large-scale non-coding variant analysis for research and clinical applications.
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