Lerna: Transformer Architectures for Configuring Error Correction Tools for Short- and Long-Read Genome Sequencing
Atul Sharma, Pranjal Jain, Ashraf Mahgoub, Zihan Zhou, Kanak Mahadik,, and Somali Chaterji

TL;DR
Lerna introduces an automated, reference-free method using language models to optimize error correction parameters in genome sequencing, significantly improving efficiency and assembly quality.
Contribution
The paper presents Lerna, a novel approach that leverages language models and perplexity metrics to automatically configure error correction tools without reference genomes.
Findings
Optimal k-mer varies across datasets and tools.
Perplexity correlates with correction quality and assembly outcomes.
Lerna achieves 18X faster runtime than previous methods.
Abstract
Sequencing technologies are prone to errors, making error correction (EC) necessary for downstream applications. EC tools need to be manually configured for optimal performance. We find that the optimal parameters (e.g., k-mer size) are both tool- and dataset-dependent. Moreover, evaluating the performance (i.e., Alignment-rate or Gain) of a given tool usually relies on a reference genome, but quality reference genomes are not always available. We introduce Lerna for the automated configuration of k-mer-based EC tools. Lerna first creates a language model (LM) of the uncorrected genomic reads; then, calculates the perplexity metric to evaluate the corrected reads for different parameter choices. Next, it finds the one that produces the highest alignment rate without using a reference genome. The fundamental intuition of our approach is that the perplexity metric is inversely correlated…
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Taxonomy
TopicsGenomics and Phylogenetic Studies · RNA and protein synthesis mechanisms · Chromosomal and Genetic Variations
