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Biomedical subjects

Xiaofang Jiang

Publications and source records attributed to Xiaofang Jiang.

3 recordsLinked to original sources

LAMBDA: a prophage detection benchmark for genomic language models.

Transformer-based genomic sequence models represent an emerging frontier in computational biology. Yet, their embeddings have not yet shown the same level of predictive power as natural and protein language models, highlighting a gap between current implementations and theoretical promise. Existing benchmarks for DNA language models primarily focus on classifying regulatory elements in eukaryotic genomes, leaving open the fundamental question of whether these models learn sequence-level features across whole genomes. We introduce LAMBDA, a benchmark designed to rigorously evaluate genome language model embeddings through phage-bacteria sequence discrimination across four categories of increasing complexity: probing tasks, fine-tuning assessments, diagnostic tests, and genome-wide prophage detection. Our comprehensive analysis of current genomic language models provides insight into the importance of training data selection relative to model size, the need for domain-specific training, and the capabilities and limitations of genomic language models for detecting prophage sequences. This benchmark represents a challenging genomic annotation task in the bacterial domain and addresses a key computational problem with direct relevance to microbiology and medicine.

Prophages

LAMBDA: A Prophage Detection Benchmark for Genomic Language Models.

Transformer-based genomic sequence models represent an emerging frontier in computational biology. Yet, their embeddings have not yet shown the same level of predictive power as natural and protein language models, indicating a gap between current implementations and theoretical promise. Existing benchmarks for DNA language models primarily focus on classifying regulatory elements in eukaryotic genomes, leaving open the fundamental question of whether these models learn sequence-level features across whole genomes. We introduce LAMBDA, a benchmark designed to rigorously evaluate genome language model embeddings through phage-bacteria sequence discrimination across four categories of increasing complexity: probing tasks, fine-tuning assessments, diagnostic tests, and genome-wide prophage detection. Our comprehensive analysis of current genomic language models provides novel insights into the importance of training data quality relative to model size, the need for domain-specific training, and the application of genomic language models for detecting prophage sequences. This benchmark represents a challenging genomic annotation task in the bacterial domain and addresses a key computational problem with direct relevance to microbiology and medicine.

DNA language model

The impact of tokenizer selection in genomic language models.

MOTIVATION: Genomic language models have recently emerged as a new method to decode, interpret, and generate genetic sequences. Existing genomic language models have utilized various tokenization methods, including character tokenization, overlapping and nonoverlapping k-mer tokenization, and byte-pair encoding, a method widely used in natural language models. Genomic sequences differ from natural language because of their low character variability, complex and overlapping features, and inconsistent directionality. These features make subword tokenization in genomic language models significantly different from both traditional language models and protein language models. RESULTS: This study explores the impact of tokenization in genomic language models by evaluating their downstream performance on 44 classification fine-tuning tasks. We also perform a direct comparison of byte pair encoding and character tokenization in Mamba, a state-space model. Our results indicate that character tokenization outperforms subword tokenization methods on tasks that rely on nucleotide-level resolution, such as splice site prediction and promoter detection. While byte-pair tokenization had stronger performance on the SARS-CoV-2 variant classification task, we observed limited statistically significant differences between tokenization methods on the remaining downstream tasks. AVAILABILITY AND IMPLEMENTATION: Detailed results of all benchmarking experiments are available in https://github.com/leannmlindsey/DNAtokenization. Training datasets and pretrained models are available at https://huggingface.co/datasets/leannmlindsey. Datasets and processing scripts are available at doi: 10.5281/zenodo.16287401 and doi: 10.5281/zenodo.16287130.

Natural Language Processing