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Kiss, E.

Publications and source records attributed to Kiss, E..

2 recordsLinked to original sources

Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease

Methylation patterns of circulating cell-free DNA (cfDNA) contain rich information about recent cell death events in the body. Here, we present an approach for unbiased determination of the tissue origins of cfDNA, using a reference methylation atlas of 25 human tissues and cell types. The method is validated using in silico simulations as well as in vitro mixes of DNA from different tissue sources at known proportions. We show that plasma cfDNA of healthy donors originates from white blood cells (55%), erythrocyte progenitors (30%), vascular endothelial cells (10%) and hepatocytes (1%). Deconvolution of cfDNA from patients reveals tissue contributions that agree with clinical findings in sepsis, islet transplantation, cancer of the colon, lung, breast and prostate, and cancer of unknown primary. We propose a procedure which can be easily adapted to study the cellular contributors to cfDNA in many settings, opening a broad window into healthy and pathologic human tissue dynamics.

molecular biology

Improving Accuracy of Nuclei Segmentation by Reducing Histological Image Variability

Cancer is the second leading cause of death in United States. Early diagnosis of this disease is essential for many types of treatment. Cancer is most accurately observed by pathologists using tissue biopsy. In the past, evaluation of tissue samples was done manually, but to improve efficiency and ensure consistent quality, there has been a push to evaluate these algorithmically. One important task in histological analysis is the segmentation and evaluation of nuclei. Nuclear morphology is important to understand the grade and progression of cancer. Convolutional neural networks (CNN) were used to segment train models for nuclei segmentation. Stains are used to highlight cellular features. However, there is significant variability in imaging of stained slides due to differences in stain, slide preparation and slide storage. This make automated methods challenging to implement across different datasets. This paper evaluates four stain normalization methods to reduce the variability between slides. Nuclear segmentation accuracy was evaluated for each normalized method. Baseline segmentation accuracy was improved by more than 50% of its base value as measured by the AUC and Recall. We believe this is the first study to look at the impact of four stain normalization approaches (histogram equalization, Reinhart, Macenko, Khan) on segmentation accuracy.

pathology