Rapid Proteome‐Wide Discovery of Protein–Protein Interactions With ppIRIS
ppIRIS is a lightweight deep learning framework for proteome‐wide protein–protein interaction prediction directly from sequence. By fusing evolutionary and structural embeddings with a regularized Siamese architecture, ppIRIS achieves state‐of‐the‐art accuracy across species, enables minute‐scale screening, and reveals biologically validated bacterial ...
Luiz Felipe Piochi +4 more
wiley +1 more source
Assessing Genotype Imputation Methods for Low-Coverage Sequencing Data in Populations With Differing Relatedness and Inbreeding Levels. [PDF]
Vi T +4 more
europepmc +1 more source
Imputation methods for missing failure times in recurrent-event survival analysis: Application to suicide attempts in the transgender population. [PDF]
Liu S, Reisner SL, Herman JL, Weller E.
europepmc +1 more source
Leveraging Artificial Intelligence and Large Language Models for Cancer Immunotherapy
Cancer immunotherapy faces challenges in predicting treatment responses and understanding resistance mechanisms. Artificial intelligence (AI) and machine learning (ML) offer powerful solutions for cancer immunotherapy in patient stratification, biomarker discovery, treatment strategy optimization, and foundation model development.
Xinchao Wu +4 more
wiley +1 more source
This work establishes a pipeline that transforms fragmented literature into a structured database for graphitic carbon nitride photocatalyst discovery. A prompt‐engineered, cross‐model large language model ensemble automates high‐fidelity extraction, enabling interpretable machine learning to identify dominant performance descriptors. These data‐driven
Dianyuan Li +7 more
wiley +1 more source
The impact of missing data rates and imputation methods on the assumption of unidimensionality. [PDF]
Baniamer AO.
europepmc +1 more source
scIMC: a platform for benchmarking comparison and visualization analysis of scRNA-seq data imputation methods. [PDF]
Dai C +7 more
europepmc +1 more source
PAIR: Reconstructing Single‐Cell Open‐Chromatin Landscapes for Transcription Factor Regulome Mapping
scATAC‐seq analysis is often constrained by limited sequencing depth, extreme sparsity, and pervasive technical missingness. PAIR is a probabilistic framework that restores scATAC‐seq accessibility profiles by directly modeling the native cell–peak bipartite structure of chromatin accessibility.
Yanchi Su +7 more
wiley +1 more source
Bridging the Gap: Missing Data Imputation Methods and Their Effect on Dementia Classification Performance. [PDF]
Aracri F +3 more
europepmc +1 more source
Are dropout imputation methods for scRNA-seq effective for scHi-C data? [PDF]
Han C, Xie Q, Lin S.
europepmc +1 more source

