A hybrid cell image segmentation method based on the multilevel improvement of data.

Over the years, several methods have been developed for the segmentation of cell images. Most of the related techniques operate directly on the raw data (noisy cell samples) of the medical image which leads to adverse effects on the structure of leucocytes because the medical images are affected by multiple distortions (varying illumination, deficient background light intensity, and non-uniform staining). To overcome these problems, we came up with an improved solution that performs the qualitative enhancement of cell images for the smooth extraction of cell-nucleus. Although various segmentation methods have adopted an image improvement operation in practice. These methods also amplify the magnitude of image noise which leads to over-sampling and under-sampling of data points. This mis-labelling of data points is minimized by the developed approach which adopts a collaborative fusion strategy (CNN and Nuclear-norm approach) for the qualitative improvement of cell images. The enhanced cell samples were forwarded to the U-net (deep learning model) model for the semantic segmentation of cell images. The performance evaluation of the model was performed on three biomedical cell imaging datasets, which include the ALL-IDB (99.89% accuracy, 99.51% recall, and 99.01% precision), CellaVision (99.68% accuracy, 98.75% precision, and 97.94% specificity) and JTSC (98.45% accuracy, 97.42% precision, and 97.21% specificity) dataset. The results were compared with the state-of-art methods in which the adopted hybrid approach has overpowered the related techniques in the quantitative and qualitative domains.

Robust correlation estimation and UMAP assisted topological analysis of omics data for disease subtyping.

Deciphering information hidden in the gene expression assays for identifying disease subtypes has significant importance in precision medicine. However, computational limitations thwart this process due to the intricacy of the biological networks and the curse of dimensionality of gene expression data. Therefore, clustering in such scenarios often becomes the first choice of exploratory data analysis to identify natural structures and intrinsic patterns in the data. However, sparse and high dimensional nature of omics data prevents conventional clustering algorithms to discover subtypes that are clinically relevant and statistically significant. Hence, non-linear dimensionality reduction techniques coupled with clustering in such scenarios often becomes imperative to improve the clustering results. In this study, we present a robust pipeline to discover disease subtypes with clinical relevance. Specifically, we focus on discovering patient sub-groups that have a residual life patterns remarkably different from other sub-groups. This is significant because by refining prognosis, subtyping can reduce uncertainty in approximating patients expected outcome. The methodology present is based on robust correlation estimation, UMAP- a non-linear dimensionality reduction method and mapper- a tool from topology. Notably, we suggest a method for improving the robustness of the correlation matrix of gene expression data for improving the clustering results. The performance of the model is evaluated by applying to five cancer datasets obtained through TCGA and comparisons are performed with some state of the art methods of NEMO, RSC-OTRI and SNF with regard to log-rank test and Restricted Life Expectancy Difference. For example in GBM dataset, the minimum separation for any two discovered subtypes is 221 days which is significantly higher than the other methodologies. We also compared the results without using the robust correlation based estimate and observed that robust correlation improves separability between survival curves significantly. From the results we infer that our methodology performs better compared to other methodologies with regard to separating survival curves of patient sub-groups despite using single omics profiles of patients compared to multiple omics profiles of SNF and NEMO. Pathway over-representation analysis is performed on the final clustering results to investigate the biological underpinnings characterizing each subtype.

An enforced block diagonal low-rank representation method for the classification of medical image patterns.

Low-rank representation based methods have been used on a variety of medical imaging databases for the segmentation and classification of biomedical images. The subspace segmentation of the data is performed by generating the block diagonal coefficient matrix. Whereas, the data is classified by performing the partitioning of the low-rank representation matrix. There exist several such methods for analysing medical images. The major difference between them lies in the construction of the data dictionary. Most of the time, the input data pattern is used as the dictionary for learning the representation matrix. The direct use of the input data for learning the representation degrades the performance of the model because medical images are subjected to outliers of multiple types, which include environmental lighting, image appearance and varying illumination. These types of errors induce noise in the data. It has been observed that the representation-based model is robust when the training data is clean. If the training data contains corrupted subsamples, the performance of the model drops down. We have addressed the mentioned problem by adopting a class-wise dictionary learning approach. In which the pattern of each class is learnt as the set of tuples in the dictionary. The model has been evaluated on several medical imaging datasets, which includes the Break-his dataset, ALL-IDB, biomedical images, covid CT and chest X-ray. The classification performance of the model is best for the biomedical database (99.16%) followed by the Covid dataset (94%), ALL-IDB database (93.47%) and Break-his dataset (93%).