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Multi-spectral imaging technique plays an important role in real-world applications such as medicine and medical detections. This paper proposes a cervical cancer cell screening method to simultaneously adopt TBS classification and DNA quantitative analysis for a single cell smear. Through using compound staining on a smear, the cytoplasm is stained by Papanicolauo and the nucleus is stained by Feulgen. The main evaluation parameter is the DNA content of the nucleus, not the subjective description of cell morphology, which is more objective than the TBS classification method and reduces the chances of missing a diagnosis due to subjective factors. Each nucleus has its own DI value and color image of the whole cell, which is convenient for doctors as it allows them to review and confirm the morphology of cells with a nucleus DI of over 2.5. Mouse liver smears and cervical cases are utilized as the measuring specimens to evaluate the performance of the microscope multi-spectral imaging system, illustrative results demonstrate that the proposed system qualifies, with high accuracy and reliability, and further presents wide application prospects in the early diagnosis of cervical cancer.

Development of an accurate and automated algorithm to completely segment cervical cells in Pap images is still one of the most challenging tasks. The main reasons are the presence of overlapping cells and the lack of guiding mechanism for the convergence of ill-defined contours to the actual cytoplasm boundaries. In this paper, we propose a novel method to address these problems based on level set method (LSM). Firstly, we proposed a morphological scaling-based topology filter (MSTF) and derived a new mathematical toolbox about vector calculus for evolution of level set function (LSF). Secondly, we combine MSTF and the mathematical toolbox into a multifunctional filtering algorithm 2D codimension two-object level set method (DCTLSM) to split touching cells. The DCTLSM can morphologically scale up and down the contour while keeping part of the contour points fixed. Thirdly, we design a contour scanning strategy as the evolution method of LSF to segment overlapping cells. In this strategy, a cutting line can be detected by morphologically scaling the union LSF of the pairs of cells. Then, we used this cutting line to construct a velocity field with an effective guiding mechanism for attracting and repelling LSF. The performance of the proposed algorithm was evaluated quantitatively and qualitatively on the ISBI-2014 dataset. The experimental results demonstrated that the proposed method is capable of fully segmenting cervical cells with superior segmentation accuracy compared with recent peer works.