Recent advances in immunology and synthetic biology have accelerated the development of deep generative methods for DNA sequence design. Two dominant approaches in this field are AutoRegressive (AR) models and Diffusion Models (DMs). However, genomic sequences are functionally heterogeneous, consisting of multiple connected regions (e.g., Promoter Regions, Exons, and Introns) where elements within each region come from the same probability distribution, but the overall sequence is non-homogeneous. This heterogeneous nature presents challenges for a single model to accurately generate genomic sequences. In this paper, we analyze the properties of AR models and DMs in heterogeneous genomic sequence generation, pointing out crucial limitations in both methods: (i) AR models capture the underlying distribution of data by factorizing and learning the transition probability but fail to capture the global property of DNA sequences.

We consider controllable DNA sequence design, where sequences are generated by conditioning on specific biological properties. While language models (LMs) such as GPT and BERT have achieved remarkable success in natural language generation, their application to DNA sequence generation remains largely underexplored. In this work, we introduce ATGC-Gen, an Automated Transformer Generator for Controllable Generation, which leverages cross-modal encoding to integrate diverse biological signals. ATGC-Gen is instantiated with both decoder-only and encoder-only transformer architectures, allowing flexible training and generation under either autoregressive or masked recovery objectives. We evaluate ATGC-Gen on representative tasks including promoter and enhancer sequence design, and further introduce a new dataset based on ChIP-Seq experiments for modeling protein binding specificity. Our experiments demonstrate that ATGC-Gen can generate fluent, diverse, and biologically relevant sequences aligned with the desired properties. Compared to prior methods, our model achieves notable improvements in controllability and functional relevance, highlighting the potential of language models in advancing programmable genomic design.

Assessing risk of bias (RoB) in randomized controlled trials is essential for trustworthy evidence synthesis, but the process is resource-intensive and prone to variability across reviewers. Large language models (LLMs) offer a route to automation, but existing methods rely on manually engineered prompts that are difficult to reproduce, generalize, or evaluate. This study introduces a programmable RoB assessment pipeline that replaces ad-hoc prompt design with structured, code-based optimization using DSPy and its GEPA module. GEPA refines LLM reasoning through Pareto-guided search and produces inspectable execution traces, enabling transparent replication of every step in the optimization process. We evaluated the method on 100 RCTs from published meta-analyses across seven RoB domains. GEPA-generated prompts were applied to both open-weight models (Mistral Small 3.1 with GPT-oss-20b) and commercial models (GPT-5 Nano and GPT-5 Mini). In domains with clearer methodological reporting, such as Random Sequence Generation, GEPA-generated prompts performed best, with similar results for Allocation Concealment and Blinding of Participants, while the commercial model performed slightly better overall. We also compared GEPA with three manually designed prompts using Claude 3.5 Sonnet. GEPA achieved the highest overall accuracy and improved performance by 30%-40% in Random Sequence Generation and Selective Reporting, and showed generally comparable, competitively aligned performance in the other domains relative to manual prompts. These findings suggest that GEPA can produce consistent and reproducible prompts for RoB assessment, supporting the structured and principled use of LLMs in evidence synthesis.

The encoder-decoder framework has achieved promising progress for many sequence generation tasks, including machine translation, text summarization, dialog system, image captioning, etc. Such a framework adopts an one-pass forward process while decoding and generating a sequence, but lacks the deliberation process: A generated sequence is directly used as final output without further polishing. However, deliberation is a common behavior in human's daily life like reading news and writing papers/articles/books. In this work, we introduce the deliberation process into the encoder-decoder framework and propose deliberation networks for sequence generation. A deliberation network has two levels of decoders, where the first-pass decoder generates a raw sequence and the second-pass decoder polishes and refines the raw sentence with deliberation. Since the second-pass deliberation decoder has global information about what the sequence to be generated might be, it has the potential to generate a better sequence by looking into future words in the raw sentence. Experiments on neural machine translation and text summarization demonstrate the effectiveness of the proposed deliberation networks. On the WMT 2014 English-to-French translation task, our model establishes a new state-of-the-art BLEU score of 41.5.

This heterogeneous nature presents challenges for a single model to accurately generate genomic sequences.

Abstract--Computational protein design is experiencing a transformation driven by AI/ML. However, the range of potential protein sequences and structures is astronomically vast, even for moderately sized proteins. Hence, achieving convergence between generated and predicted structures demands substantial computational resources for sampling. The Integrated Machine-learning for Protein Structures at Scale (IMPRESS) offers methods and advanced computing systems for coupling AI to high-performance computing tasks, enabling the ability to evaluate the effectiveness of protein designs as they are developed, as well as the models and simulations used to generate data and train models. This paper introduces IMPRESS and demonstrates the development and implementation of an adaptive protein design protocol and its supporting computing infrastructure. This leads to increased consistency in the quality of protein design and enhanced throughput of protein design due to dynamic resource allocation and asynchronous workload execution.

We introduce HALO - a deep generative model utilising HAmiltonian Latent Operators to reliably disentangle content and motion information in image sequences.