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Xue Xiao

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3

AAAI Conference 2026 Conference Paper

GenePheno: Interpretable Gene Knockout-Induced Phenotype Abnormality Prediction from Gene Sequences

  • Jingquan Yan
  • Yuwei Miao
  • Lei Yu
  • Yuzhi Guo
  • Xue Xiao
  • Lin Xu
  • Junzhou Huang

Exploring how genetic sequences shape phenotypes is a fundamental challenge in biology and a key step toward scalable, hypothesis-driven experimentation. The task is complicated by the large modality gap between sequences and phenotypes, as well as the pleiotropic nature of gene–phenotype relationships. Existing sequence-based efforts focus on the degree to which variants of specific genes alter a limited set of phenotypes, while general gene knockout-induced phenotype abnormality prediction methods heavily rely on curated genetic information as inputs, which limits scalability and generalizability. As a result, the task of broadly predicting the presence of multiple phenotype abnormalities under gene knockout directly from gene sequences remains underexplored. We introduce GenePheno, the first interpretable multi-label prediction framework that predicts knockout-induced phenotypic abnormalities from gene sequences. GenePheno employs a contrastive multi-label learning objective that captures inter-phenotype correlations, complemented by an exclusive regularization that enforces biological consistency. It further incorporates a gene function bottleneck layer, offering human-interpretable concepts that reflect functional mechanisms behind phenotype formation. To support progress in this area, we curate four datasets with canonical gene sequences as input and multi-label phenotypic abnormalities induced by gene knockouts as targets. Across these datasets, GenePheno achieves state-of-the-art gene-centric Fmax and phenotype-centric AUC, and case studies demonstrate its ability to reveal gene functional mechanisms.

AAAI Conference 2026 Conference Paper

Sample Weighted Incomplete Multimodal Clustering Based on Graph Coarsening Label Extraction

  • Zhenjiao Liu
  • Xue Xiao
  • Yao Chen
  • Jiao Xue
  • Shubin Ma
  • Liang Zhao

Multimodal data is typically collected through heterogeneous sensors and processing pipelines. However, due to variations in acquisition environments, device capabilities, and feature extraction methods, such data often suffers from incompleteness and inconsistent quality across modalities. To address these challenges, prior studies have explored modality selection and data completion strategies to improve information fusion. Nevertheless, these approaches face two main limitations: (1) they struggle to simultaneously ensure computational efficiency for large-scale graph data and maintain structural and semantic consistency across heterogeneous modality graphs; and (2) most of them operate at the modality level and fail to capture fine-grained, sample-specific quality variations. To overcome these issues, we propose a novel clustering framework, Sample Weighted Incomplete Multimodal Clustering Based on Graph Coarsening Label Extraction (IMC-GCSW). The proposed method introduces a graph coarsening-based label extraction strategy. It significantly reduces the computational cost of multimodal graph processing, while preserving key node information and local topological structures. Furthermore, a quality-aware sample weighting strategy is designed to enable fine-grained modeling of modality-specific data quality, allowing the model to dynamically suppress the influence of low-quality modalities on individual samples. Experiments on both general-purpose datasets and the Fructus Aurantii Disease and Pest Datasets demonstrate that the proposed method exhibits superior performance and strong adaptability in handling multimodal data with incompleteness and quality inconsistency.