Journal of Chemical Information and ModelingBioinformaticsPeer-reviewed journal article
DNACSE: Enhancing Genomic LLMs with Contrastive Learning for DNA Barcode Identification
Jiadong WangiD, Bin WangiD, Shihua ZhouiD, Ben CaoiD, Wei Li, Pan ZhengiD
Abstract
DNA barcoding is a powerful tool for exploring biodiversity, and DNA language models have significantly facilitated its construction and identification. However, since DNA barcodes come from a specific region of mitochondrial DNA and there are structural differences between DNA barcodes and reference genomes used to train existing DNA language models, it is difficult to directly apply the existing DNA language models to the DNA barcoding task. To address this, this paper introduce DNACSE (DNA Contrastive Learning for Sequence Embeddings), an unsupervised noise contrastive learning framework designed to fine-tune the DNA language foundation model while enhancing the distribution of the embedding space. The results demonstrate that DNACSE outperforms direct usage of DNA language models in DNA barcoding-related tasks. Specifically, in fine-tuning and linear probe tasks, it achieves accuracy rates of 99.17% and 98.31%, respectively, surpassing the current state-of-the-art BarcodeBERT by 6.44% and 6.44%. In zero-shot clustering tasks, it raises the Adjusted Mutual Information (AMI) score to 92.25%, an improvement of 8.36%. In addition, zero-shot benchmarking and genomic benchmarking tests are evaluated, indicating that DNACSE enhances the performance of DNA language models in generalized genomic tasks. In summary, DNACSE has demonstrated excellent performance in DNA barcode species classification by making full use of multi-species information and DNA barcode information, providing a feasible way to further explore and protect biodiversity. The code repository is available at https://github.com/Kavicy/DNACSE.
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: cell type annotation
- approach: contrastive learning
- Citations
- 8
- FWCI
- 16.42
- Field percentile
- top 1%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Back to BERT in 2026: ModernGENA as a Strong, Efficient Baseline for DNA Foundation Models
Alena Aspidova, Yuri Kuratov, … Veniamin Fishman·bioRxiv·Apr 23, 2026
- Carbon: Decoding the Language of Life
Loubna Ben Allal, Qiuyi Li, … Leandro von Werra·bioRxiv·May 25, 2026
- genomicBERT: A Light-weight Foundation Model for Genome Analysis using Unigram Tokenization and Specialized DNA Vocabulary
Tyrone Chen, Naima Vahab, … Sonika Tyagi·bioRxiv·May 31, 2023
- Distinguishing word identity and sequence context in DNA language models
Melissa Sanabria, Jonas Hirsch, Anna R. Poetsch·BMC BioinformaticsPeer-reviewed·Sep 13, 2024
- DNA-LLM2Vec: Architecture-Aware Task-Conditioned Adaptation of Decoder DNA Foundation Models
Yuan Liang, Ke Zhai, … Massimo Poesio·bioRxiv·Oct 14, 2026
- DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome
Yanrong Ji, Zhihan Zhou, … Ramana V. Davuluri·BioinformaticsPeer-reviewed·Feb 3, 2021