Cancer Data
This is a two-part open-access page -'Data:B-Bio Models-1 and 'Data:B-Bio Models-2'. This webpage contains datasets and models, with clinical investigation in simulation, proposed by me which are Self-Claimed advancements. All the content can be freely downloaded after sign-up.
I. Novel B-Bio Models
To freely download, pls. click on title. Make sure you have read My ORCid, Disclaimer and Legal Disclosure Statement.
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Image : Image was made by me for other International Contest (held by some Medical Institute,USA in the year 2021), 'An intuitive of electromagnetic radiation flowing over epithelial tissue'.
This is an open-access page. All content can be freely downloaded after sign-up. This webpage contains datasets and models, which are in support of my Research, Discovery and Claim.
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Microscopic image based analysis plays an important role in histopathological computer based diagnostics. Identification of childhood medulloblastoma and its proper subtype from biopsy tissue specimen of childhood tumor is an integral part for prognosis.The dataset is of Childhood medulloblastoma (CMB) biopsy samples. The images are of 10x and 100x microscopic magnifications, uploaded in separate folders. The images consist of normal brain tissue cell samples and CMB cell samples of different WHO defined subtypes. An excel sheet is also uploaded for ease of data description.
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Supplementary materials (Table S2).
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Proteome analysis of extracellular vesicles, isolated from murine breast cancer cells or serum of healthy mice.
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The migration of cancer cells is highly regulated by the biomechanical properties of their local microenvironment. Using 3D scaffolds of simple composition, several aspects of cancer cell mechanosensing (signal transduction, EMC remodeling, traction forces) have been separately analyzed in the context of cell migration. However, a combined study of these factors in 3D scaffolds that more closely resemble the complex microenvironment of the cancer ECM is still missing.
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Hyperspectral (HS) imaging presents itself as a non-contact, non-ionizing and non-invasive technique, proven to be suitable for medical diagnosis. However, the volume of information contained in these images makes difficult providing the surgeon with information about the boundaries in real-time. To that end, High-Performance-Computing (HPC) platforms become necessary. This paper presents a comparison between the performances provided by five different HPC platforms while processing a spatial-spectral approach to classify HS images, assessing their main benefits and drawbacks.
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Monitoring cell viability and proliferation in real-time provides a more comprehensive picture of the changes cells undergo during their lifecycle than can be achieved using traditional end-point assays. Our lab has developed a CMOS biosensor that monitors cell viability through high-resolution capacitance measurements of cell adhesion quality. The system consists of a 3 × 3 mm2 chip with an array of 16 sensors, on-chip digitization, and serial data output that can be interfaced with inexpensive off-the-shelf components.
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Malignant pleural effusions (MPEs) are a challenging public health problem, causing significant morbidity and often being the first presenting sign of cancer. Pleural fluid cytology is the most common method used to differentiate malignant from non-malignant effusions. However, its sensitivity reaches 50-70% and depends on the experience of the cytologist, the tumor load, and the amount of fluid tested. Therefore, diagnostic inaccuracy and a high incidence of false negatives may endanger patients with clinical mistreatment and mismanagement.
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