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Background: Prompt-based learning involves the additions of prompts (i.e., templates) to the input of pre-trained large language models (PLMs) to adapt them to specific tasks with minimal training. This technique is particularly advantageous in clinical scenarios where the amount of annotated data is limited. This study aims to investigate the impact of template position on model performance and training efficiency in clinical note classification tasks using prompt-based learning, especially in zero- and few-shot settings.
Methods: We developed a keyword-optimized template insertion method (KOTI) to enhance model performance by strategically placing prompt templates near relevant clinical information within the notes. The method involves defining task-specific keywords, identifying sentences containing these keywords, and inserting the prompt template in their vicinity. We compared KOTI with standard template insertion (STI) methods in which the template is directly appended at the end of the input text. Specifically, we compared STI with naïve tail-truncation (STI-s) and STI with keyword-optimized input truncation (STI-k). Experiments were conducted using two pre-trained encoder models, GatorTron and ClinicalBERT, and two decoder models, BioGPT and ClinicalT5, across five classification tasks, including dysmenorrhea, peripheral vascular disease, depression, osteoarthritis, and smoking status classification.
Results: Our experiments revealed that the KOTI approach consistently outperformed both STI-s and STI-k in zero-shot and few-shot scenarios for encoder models, with KOTI yielding a significant 24% F1 improvement over STI-k for GatorTron and 8% for Clinical BERT. Additionally, training with balanced examples further enhanced performance, particularly under few-shot conditions. In contrast, decoder-based models exhibited inconsistent results, with KOTI showing significant improvement in F1 score over STI-k for BioGPT (+19%), but a significant drop for ClinicalT5 (-18%), suggesting that KOTI is not beneficial across all transformer model architectures.
Conclusion: Our findings underscore the significance of template position in prompt-based fine-tuning of encoder models and highlights KOTI's potential to optimize real-world clinical note classification tasks with few training examples.
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http://dx.doi.org/10.1186/s12911-025-03071-y | DOI Listing |
Mol Ther
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Be Biopharma, Cambridge, MA, 02139, USA. Electronic address:
Hemophilia B gene therapy treatments currently have not addressed the need for predictable, durable, active, and redosable factor IX (FIX). Unlike conventional gene therapy, engineered B Cell Medicines (BCMs) are durable, redosable, and titratable, and thus have the potential to address significant unmet needs in the Hemophilia B treatment paradigm. BE-101 is an autologous BCM comprised of expanded and differentiated B lymphocyte lineage cells genetically engineered ex vivo to secrete FIX-Padua.
View Article and Find Full Text PDFRSC Adv
August 2025
Key Laboratory of Engineering Plastics, Beijing National Laboratory for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences Beijing 100190 China
Iminopyridine nickel catalysts are typically prone to facile chain transfer reactions, resulting in low molecular weight polyethylenes. In this study, a spatial proximity strategy was employed in 5-dibenzosuberyl-modified iminopyridine nickel catalysts to enhance ethylene polymerization. Using a template reaction between acetylpyridine and 5-dibenzosuberyl-functionalized aniline, a series of 2-(1-(2,6-bis(5-dibenzosuberyl)-4-(alkyl)phenylimino)ethyl)pyridine ligands were synthesized and subsequently reacted with (1,2-dimethoxyethane)NiBr to afford the corresponding nickel complexes.
View Article and Find Full Text PDFNat Biotechnol
September 2025
Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), Würzburg, Germany.
Base editors create precise genomic edits by directing nucleobase deamination or removal without inducing double-stranded DNA breaks. However, a vast chemical space of other DNA modifications remains to be explored for genome editing. Here we harness the bacterial antiphage toxin DarT2 to append ADP-ribosyl moieties to DNA, unlocking distinct editing outcomes in bacteria versus eukaryotes.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Department of Chemistry and International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208.
Genome editing with CRISPR-Cas systems hold promise for treating a wide range of genetic disorders and cancers. However, efficient delivery of genome editors remains challenging due to the requirement for the simultaneous delivery or intracellular generation of Cas proteins, guide RNAs, and, in some applications, donor DNAs. Furthermore, the immunogenicity and toxicity of delivery vehicles can limit the safety and efficacy of genetic medicines.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Emeritus, Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Many genomics specialists recognize that the massive genome rearrangements grouped under the term "chromoanagenesis" are a path to rapid evolutionary change by restructuring chromosomes, creating chimeric sequence combinations, and altering regulatory interactions leading to novel phenotypes. Less attention has been paid to the role of ubiquitous eukaryotic double-strand DNA break repair functions known as "alternative end-joining" (AltEJ) in generating additional DNA sequence innovation. A close look at some examples of chromoanagenesis rearrangements in the human germline and tumor cells illustrates how diverse these novel sequences can be.
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