ArticleInterdisciplinary sciences, computational life sciences2026
LLM4PDA: Augmenting piRNA-Disease Association Prediction with Large Language Models.
Article in Interdisciplinary sciences, computational life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
PIWI-interacting RNAs (piRNAs) maintain genomic stability by interacting with PIWI proteins and have been implicated in various human diseases. However, wet-lab experiments remain limited in throughput, creating an urgent need for computational methods to systematically identify piRNA-disease associations. Although numerous computational approaches have been proposed, they still face major challenges such as limited feature representations and insufficient integration of biological knowledge. This study presents LLM4PDA, a large language model-augmented framework for piRNA-disease association prediction. PiRNA sequences are encoded using RNA-FM, whereas disease representations are derived from LLM-generated disease descriptions guided by a reusable, structured prompt template and encoded using OpenAI's text-embedding models. These representations are mapped into a common latent space through an MLP-based alignment module, enabling association scoring for candidate piRNA-disease pairs. Separately from the predictive model, a post-prediction interpretive module organizes high-confidence predictions into structured, knowledge-informed biological summaries to support hypothesis generation and guide downstream experimental validation. Five-fold cross-validation demonstrates that LLM4PDA achieves area under the curve (AUC) values of 0.984 and 0.985 on two benchmark datasets, outperforming eight state-of-the-art methods. Case studies further illustrate how the interpretive module facilitates structured synthesis of biological context for selected high-confidence associations.
Indexed as
Identifiers
42870191What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.