Jiaxin Qi

Jiaxin Qi, Yulei Niu, Jianqiang Huang et al.

This paper unravels the design tricks adopted by us, the champion team MReaL-BDAI, for Visual Dialog Challenge 2019: two causal principles for improving Visual Dialog (VisDial). By "improving", we mean that they can promote almost every existing VisDial model to the state-of-the-art performance on the leader-board. Such a major improvement is only due to our careful inspection on the causality behind the model and data, finding that the community has overlooked two causalities in VisDial. Intuitively, Principle 1 suggests: we should remove the direct input of the dialog history to the answer model, otherwise a harmful shortcut bias will be introduced; Principle 2 says: there is an unobserved confounder for history, question, and answer, leading to spurious correlations from training data. In particular, to remove the confounder suggested in Principle 2, we propose several causal intervention algorithms, which make the training fundamentally different from the traditional likelihood estimation. Note that the two principles are model-agnostic, so they are applicable in any VisDial model. The code is available at https://github.com/simpleshinobu/visdial-principles.

Yishun Zhu, Jiaxin Qi, Jian Wang et al.

Spatial Transcriptomics (ST) profiles thousands of gene expression values at discrete spots with precise coordinates on tissue sections, preserving spatial context essential for clinical and pathological studies. With rising sequencing throughput and advancing platforms, the expanding data volumes motivate large-scale ST pretraining. However, the fundamental unit for pretraining, i.e., what constitutes a single training sample, remains ill-posed. Existing choices fall into two camps: (1) treating each spot as an independent sample, which discards spatial dependencies and collapses ST into single-cell transcriptomics; and (2) treating an entire slide as a single sample, which produces prohibitively large inputs and drastically fewer training examples, undermining effective pretraining. To address this gap, we propose treating spatial transcriptomics as croppable images. Specifically, we define a multi-channel image representation with fixed spatial size by cropping patches from raw slides, thereby preserving spatial context while substantially increasing the number of training samples. Along the channel dimension, we define gene subset selection rules to control input dimensionality and improve pretraining stability. Extensive experiments show that the proposed image-like dataset construction for ST pretraining consistently improves downstream performance, outperforming conventional pretraining schemes. Ablation studies verify that both spatial patching and channel design are necessary, establishing a unified, practical paradigm for organizing ST data and enabling large-scale pretraining.

Jiaxin Qi, Yan Cui, Jianqiang Huang et al.

Classes, as fundamental elements of Computer Vision, have been extensively studied within incremental learning frameworks. In contrast, tokens, which play essential roles in many research fields, exhibit similar characteristics of growth, yet investigations into their incremental learning remain significantly scarce. This research gap primarily stems from the holistic nature of tokens in language, which imposes significant challenges on the design of incremental learning frameworks for them. To overcome this obstacle, in this work, we turn to a type of token, gene, for a large-scale biological dataset--single-cell transcriptomics--to formulate a pipeline for gene incremental learning and establish corresponding evaluations. We found that the forgetting problem also exists in gene incremental learning, thus we adapted existing class incremental learning methods to mitigate the forgetting of genes. Through extensive experiments, we demonstrated the soundness of our framework design and evaluations, as well as the effectiveness of our method adaptations. Finally, we provide a complete benchmark for gene incremental learning in single-cell transcriptomics.

Zhijiang Tang, Jiaxin Qi, Yuhua Zheng et al.

Electrocardiogram~(ECG), a key bioelectrical time-series signal, is crucial for assessing cardiac health and diagnosing various diseases. Given its time-series format, ECG data is often incorporated into pre-training datasets for large-scale time-series model training. However, existing studies often overlook its unique characteristics and specialized downstream applications, which differ significantly from other time-series data, leading to an incomplete understanding of its properties. In this paper, we present an in-depth investigation of ECG signals and establish a comprehensive benchmark, which includes (1) categorizing its downstream applications into four distinct evaluation tasks, (2) identifying limitations in traditional evaluation metrics for ECG analysis, and introducing a novel metric; (3) benchmarking state-of-the-art time-series models and proposing a new architecture. Extensive experiments demonstrate that our proposed benchmark is comprehensive and robust. The results validate the effectiveness of the proposed metric and model architecture, which establish a solid foundation for advancing research in ECG signal analysis.

Jiaxin Qi, Yan Cui, Jinli Ou et al.

Graph Neural Networks (GNNs) and Transformers share significant similarities in their encoding strategies for interacting with features from nodes of interest, where Transformers use query-key scores and GNNs use edges. Compared to GNNs, which are unable to encode relative positions, Transformers leverage dynamic attention capabilities to better represent relative relationships, thereby becoming the standard backbones in large-scale sequential pre-training. However, the subtle difference prompts us to consider: if positions are no longer crucial, could we substitute Transformers with Graph Neural Networks in some fields such as Single-Cell Transcriptomics? In this paper, we first explore the similarities and differences between GNNs and Transformers, specifically in terms of relative positions. Additionally, we design a synthetic example to illustrate their equivalence where there are no relative positions between tokens in the sample. Finally, we conduct extensive experiments on a large-scale position-agnostic dataset-single-cell transcriptomics-finding that GNNs achieve competitive performance compared to Transformers while consuming fewer computation resources. These findings provide novel insights for researchers in the field of single-cell transcriptomics, challenging the prevailing notion that the Transformer is always the optimum choice.