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Jiaoyun Yang

Publications and source records attributed to Jiaoyun Yang.

4 recordsLinked to original sources

HUSH-Bench: Measuring Memory-Use Boundaries for Sensitive History in Conversational Agents

Long-term memory helps conversational agents maintain continuity across sessions, while relevance and current-turn warrant remain distinct decisions. We study this boundary under a stated conservative policy in which sensitive history shapes a response when the current turn supplies a reason to use it. We introduce HUSH-Bench, a controlled benchmark of 2,400 benign prompts paired with histories containing one marked sensitive disclosure and matched no-memory references. HUSH-Bench measures unsolicited history integration with the Unsolicited History Integration Score (UIS; 0--100, higher is worse), records whether the marked disclosure reaches the generator, and includes paired prompts that differ only in whether the user asks the assistant to use earlier context. We evaluate four models under no-memory, full-context, and three retrieval-based memory settings. Memory access raises UIS from near zero to 8.9--26.6 for one model and 51.3--83.0 for the other three. Retrieval systems expose the marked disclosure in 23.0\%--30.3\% of cases, while related sensitive entries or summaries remain available and three models continue to show high UIS. Across four generators, an explicit invitation increases target-memory uptake scores by 27.0--41.3; measured helpfulness remains stable while mean over-scope rises. These results motivate treating memory storage, retrieval, warrant, and per-turn scope as separate design decisions.

cs.AI

Few-Shot Nested Named Entity Recognition

While Named Entity Recognition (NER) is a widely studied task, making inferences of entities with only a few labeled data has been challenging, especially for entities with nested structures. Unlike flat entities, entities and their nested entities are more likely to have similar semantic feature representations, drastically increasing difficulties in classifying different entity categories in the few-shot setting. Although prior work has briefly discussed nested structures in the context of few-shot learning, to our best knowledge, this paper is the first one specifically dedicated to studying the few-shot nested NER task. Leveraging contextual dependency to distinguish nested entities, we propose a Biaffine-based Contrastive Learning (BCL) framework. We first design a Biaffine span representation module for learning the contextual span dependency representation for each entity span rather than only learning its semantic representation. We then merge these two representations by the residual connection to distinguish nested entities. Finally, we build a contrastive learning framework to adjust the representation distribution for larger margin boundaries and more generalized domain transfer learning ability. We conducted experimental studies on three English, German, and Russian nested NER datasets. The results show that the BCL outperformed three baseline models on the 1-shot and 5-shot tasks in terms of F1 score.

cs.CL

A deep belief network-based method to identify proteomic risk markers for Alzheimer disease

While a large body of research has formally identified apolipoprotein E (APOE) as a major genetic risk marker for Alzheimer disease, accumulating evidence supports the notion that other risk markers may exist. The traditional Alzheimer-specific signature analysis methods, however, have not been able to make full use of rich protein expression data, especially the interaction between attributes. This paper develops a novel feature selection method to identify pathogenic factors of Alzheimer disease using the proteomic and clinical data. This approach has taken the weights of network nodes as the importance order of signaling protein expression values. After generating and evaluating the candidate subset, the method helps to select an optimal subset of proteins that achieved an accuracy greater than 90%, which is superior to traditional machine learning methods for clinical Alzheimer disease diagnosis. Besides identifying a proteomic risk marker and further reinforce the link between metabolic risk factors and Alzheimer disease, this paper also suggests that apidonectin-linked pathways are a possible therapeutic drug target.

q-bio.QM

Deep ensemble learning for Alzheimers disease classification

Ensemble learning use multiple algorithms to obtain better predictive performance than any single one of its constituent algorithms could. With growing popularity of deep learning, researchers have started to ensemble them for various purposes. Few if any, however, has used the deep learning approach as a means to ensemble algorithms. This paper presents a deep ensemble learning framework which aims to harness deep learning algorithms to integrate multisource data and tap the wisdom of experts. At the voting layer, a sparse autoencoder is trained for feature learning to reduce the correlation of attributes and diversify the base classifiers ultimately. At the stacking layer, a nonlinear feature-weighted method based on deep belief networks is proposed to rank the base classifiers which may violate the conditional independence. Neural network is used as meta classifier. At the optimizing layer, under-sampling and threshold-moving are used to cope with cost-sensitive problem. Optimized predictions are obtained based on ensemble of probabilistic predictions by similarity calculation. The proposed deep ensemble learning framework is used for Alzheimers disease classification. Experiments with the clinical dataset from national Alzheimers coordinating center demonstrate that the classification accuracy of our proposed framework is 4% better than 6 well-known ensemble approaches as well as the standard stacking algorithm. Adequate coverage of more accurate diagnostic services can be provided by utilizing the wisdom of averaged physicians. This paper points out a new way to boost the primary care of Alzheimers disease from the view of machine learning.

cs.LG