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MEHunter: transformer-based mobile element variant detection from long reads. | LitMetric

MEHunter: transformer-based mobile element variant detection from long reads.

Bioinformatics

Center for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang 150001, China.

Published: September 2024

AI Article Synopsis

  • Mobile genetic elements (MEs) are important heritable mutagens linked to genetic diseases, and their variants (MEVs) are challenging to detect accurately.
  • Long-read sequencing technologies improve the ability to identify MEVs, but issues like variable lengths and noise complicate precise detection.
  • MEHunter, a new detection tool based on a fine-tuned transformer model, outperforms existing methods in accuracy and sensitivity and can discover novel MEVs that other tools miss; it is accessible at https://github.com/120L021101/MEHunter.

Article Abstract

Summary: Mobile genetic elements (MEs) are heritable mutagens that significantly contribute to genetic diseases. The advent of long-read sequencing technologies, capable of resolving large DNA fragments, offers promising prospects for the comprehensive detection of ME variants (MEVs). However, achieving high precision while maintaining recall performance remains challenging mainly brought by the variable length and similar content of MEV signatures, which are often obscured by the noise in long reads. Here, we propose MEHunter, a high-performance MEV detection approach utilizing a fine-tuned transformer model adept at identifying potential MEVs with fragmented features. Benchmark experiments on both simulated and real datasets demonstrate that MEHunter consistently achieves higher accuracy and sensitivity than the state-of-the-art tools. Furthermore, it is capable of detecting novel potentially individual-specific MEVs that have been overlooked in published population projects.

Availability And Implementation: MEHunter is available from https://github.com/120L021101/MEHunter.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11415824PMC
http://dx.doi.org/10.1093/bioinformatics/btae557DOI Listing

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