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Zhaonan Liu

Publications and source records attributed to Zhaonan Liu.

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Disco: Densely-overlapping Cell Instance Segmentation via Adjacency-aware Collaborative Coloring

Accurate cell instance segmentation is foundational for digital pathology analysis. Existing methods based on contour detection and distance mapping still face significant challenges in processing complex and dense cellular regions. Graph coloring-based methods provide a new paradigm for this task, yet the effectiveness of this paradigm in real-world scenarios with dense overlaps and complex topologies has not been verified. Addressing this issue, we release a large-scale dataset GBC-FS 2025, which contains highly complex and dense sub-cellular nuclear arrangements. We conduct the first systematic analysis of the chromatic properties of cell adjacency graphs across four diverse datasets and reveal an important discovery: most real-world cell graphs are non-bipartite, with a high prevalence of odd-length cycles (predominantly triangles). This makes simple 2-coloring theory insufficient for handling complex tissues, while higher-chromaticity models would cause representational redundancy and optimization difficulties. Building on this observation of complex real-world contexts, we propose Disco (Densely-overlapping Cell Instance Segmentation via Adjacency-aware COllaborative Coloring), an adjacency-aware framework based on the "divide and conquer" principle. It uniquely combines a data-driven topological labeling strategy with a constrained deep learning system to resolve complex adjacency conflicts. First, "Explicit Marking" strategy transforms the topological challenge into a learnable classification task by recursively decomposing the cell graph and isolating a "conflict set." Second, "Implicit Disambiguation" mechanism resolves ambiguities in conflict regions by enforcing feature dissimilarity between different instances, enabling the model to learn separable feature representations.

cs.CV

A calibration-free method for biosensing in cell manufacturing

Chimeric antigen receptor T cell therapy has demonstrated innovative therapeutic effectiveness in fighting cancers; however, it is extremely expensive due to the intrinsic patient-to-patient variability in cell manufacturing. We propose in this work a novel calibration-free statistical framework to effectively recover critical quality attributes under the patient-to-patient variability. Specifically, we model this variability via a patient-specific calibration parameter, and use readings from multiple biosensors to construct a patient-invariance statistic, thereby alleviating the effect of the calibration parameter. A carefully formulated optimization problem and an algorithmic framework are presented to find the best patient-invariance statistic and the model parameters. Using the patient-invariance statistic, we can recover the critical quality attribute of interest, free from the calibration parameter. We demonstrate improvements of the proposed calibration-free method in different simulation experiments. In the cell manufacturing case study, our method not only effectively recovers viable cell concentration for monitoring, but also reveals insights for the cell manufacturing process.

q-bio.QM