Abstract:While M2-polarized tumor-associated macrophages (TAMs) have been established as indicators of disease aggressiveness in diffuse large B-cell lymphoma (DLBCL), traditional CD163 immunohistochemistry (IHC) remains resource-intensive. This study aims to investigate the feasibility of using deep learning to quantify TAMs directly from standard hematoxylin and eosin-stained (HE) tissue sections. Using a curated dataset of 52 patients with DLBCL, with high-resolution HE images and IHC-validated annotations (1,713 TAM instances), five architectures were evaluated: U-Net, Swin-U-Net, Cerberus-U-Net3+, YOLOv11, and HoVer-Net. High CD163 TAM density (>20.04%) was associated with significantly reduced overall survival (HR 2.73; 95% CI:1.21-6.16; p=0.012) and progression-free survival (HR 2.88; 95% CI: 1.23-6.76; p=0.011). In multivariate Cox proportional hazards analysis adjusting for IPI, molecular subtype (GCB/non-GCB per Hans algorithm), EBV status, and age, CD163 TAM density showed a prognostic trend for overall survival (HR 3.24; 95% CI: 0.94-11.15; p=0.062) and progression-free survival (HR 2.41; 95% CI: 0.80-7.32; p=0.120). Among the evaluated models, the domain-specific Cerberus-U-Net3+ achieved the highest sensitivity (Recall 0.656), while the Transformer-based Swin-U-Net demonstrated superior segmentation fidelity (Precision 0.694, F1-score 0.633). Additionally, the survival analysis based on the predicted Swin-U-Net CD163 level revealed a 20.8% cutoff point for patients with high and low CD163 levels near IHC, as well as a downward trend in overall survival among patients with higher predicted CD163 values of 2.63 (95% CI: 0.85-8.33; p=0.083). These findings suggest that deep learning architectures using shifted-window self-attention show potential as a candidate surrogate for IHC that is scalable and cost-effective for prognostic assessment of TAMs in DLBCL.
Abstract:Large Language Models (LLMs) are increasingly adopted for complex scientific text generation tasks, yet they often suffer from limitations in accuracy, consistency, and hallucination control. This thesis introduces a Parameter-Efficient Fine-Tuning (PEFT) approach tailored for GPT-like models, aiming to mitigate hallucinations and enhance reproducibility, particularly in the computational domain of mass spectrometry. We implemented Low-Rank Adaptation (LoRA) adapters to refine GPT-2, termed MS-GPT, using a specialized corpus of mass spectrometry literature. Through novel evaluation methods applied to LLMs, including BLEU, ROUGE, and Perplexity scores, the fine-tuned MS-GPT model demonstrated superior text coherence and reproducibility compared to the baseline GPT-2, confirmed through statistical analysis with the Wilcoxon rank-sum test. Further, we propose a reproducibility metric based on cosine similarity of model outputs under controlled prompts, showcasing MS-GPT's enhanced stability. This research highlights PEFT's potential to optimize LLMs for scientific contexts, reducing computational costs while improving model reliability.
Abstract:We developed an artificial intelligence approach to predict the transfer fee of a football player. This model can help clubs make better decisions about which players to buy and sell, which can lead to improved performance and increased club budgets. Having collected data on player performance, transfer fees, and other factors that might affect a player's value, we then used this data to train a machine learning model that can accurately predict a player's impact on the game. We further passed the obtained results as one of the features to the predictor of transfer fees. The model can help clubs identify players who are undervalued and who could be sold for a profit. It can also help clubs avoid overpaying for players. We believe that our model can be a valuable tool for football clubs. It can help them make better decisions about player recruitment and transfers.