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Digital Pathology Software

Cancer diagnosis relies heavily on the practice of pathology, traditionally depending on human interpretations of tissue patterns and morphology. The process is subjective, slow, and in some cases error-prone. With an increasing numbers of cancer patients and shortage of pathologists globally, there is a greater need for technical innovations to improve efficiency and objectivity in pathology analysis. However, in the era of artificial intelligence, we believe its possible to go beyond improving efficiency to harnessing new forms of data driven tumor biomarker detection to improve cancer treatment significantly. MBM is focused on the clinical development of advanced image analysis technology to pioneer these new diagnostic possibilities in prognosis and companion diagnosis.Typography

Nucleotyping

Our Nucleotyping software quantitatively analyses the chromatin structure in tumor nuclei, which reflect epigenetic modification of DNA and ultimately gene expression. This analysis results in a biomarker measurement termed as chromatin value that is used to classified tumors as homogeneous or heterogeneous. This biomarker has been clinically verified as a pan-cancer prognostic biomarker for colorectal, prostate, gynecological and lung cancers.
*Nucleotyping was licensed from Room4 (UK), and originally developed by the Institute of Cancer Genomics and Informatics (Norway).

References:
Lancet Oncology 2018, 19: 356-369.
Br J Cancer. 2016 May 24;114(11):1243-50.

Ploidy

The Ploidy Work Station performs automated quantitative analysis of chromosome copy number in tumor cells. Abnormalities of cellular DNA content (polyploidy and aneuploidy) have long been associated with tumorigenesis and recently associated with immune response modulation. DNA ploidy status is a clincally verified prognostic biomarker in colorectal, prostate and gynecological cancers.
*Ploidy Work Station was licensed from Room4 (UK), and originally developed by the Institute of Cancer Genomics and Informatics (Norway).

References:
Br J Cancer. 2014 Apr 15;110(8):2159-64.
Gynecol Oncol. 2017 Sep;146(3):596-602.
Nat Rev Clin Oncol. 2016 May;13(5):291-304.

Stroma

Fully automated quantitative analysis of tumor tissue-microenvironment ratio. Stroma measures degree of stroma invasion surrounding cancer cells. Tumor stroma is comprised of cancer-associated fibroblast, endothelial cell, myloid cell, pericyte, lymphocyte and extra-cellular matrix. Its plays an important role in tumorigenesis, tumor invasion and metastasis, and is a clinically verified biomarker for patient prognosis in colorectal and prostate cancer.

*Stroma was licensed from Room4 (UK), and originally developed by the Institute of Cancer Genomics and Informatics (Norway).

Coloprog

Coloprog is a method that combines DNA ploidy and stroma content biomarkers to create a risk profile for each patient. ColoProg has been validated in more than 3000 colorectal cancer patients. *Coloprog was licensed from Oxford Cancer Biomarkers (UK), and originally developed by the Institute of Cancer Genomics and Informatics (Norway). References: Int J Cancer. 2020 Aug 15;147(4):1228-1234. Br J Cancer. 2020 Sep;123(6):973-981. Annals of Oncology 2018, 29: 616-623Typography

Immunopath

Immunopath is an application for the visualization and automated quantification of sections stained with IHC antibodies. Immunopath is a protocol-based software, meaning that most working antibody staining protocols can be programmed using the software, resulting in an automated, objective and reproducible IHC workflow. *Immunopath was licensed from Room4 (UK), and originally developed by the Institute of Cancer Genomics and Informatics (Norway). References: Mod Pathol. 2020; 33(5): 905–915. Br J Cancer. 2019 Sep 10; 121(6): 474–482.Typography

References:
Mod Pathol. 2020; 33(5): 905–915.
Br J Cancer. 2019 Sep 10; 121(6): 474–482.

PathTool

PathTool calculates the Gleason score automatically in prostate cancer samples. Traditionally this is a subjective evaluation made by trained pathologists. PathTool provides an accurate and reproducible result that could give the patient his Gleason score within seconds, independent of a pathologist. This work is now being validated through a study at the University College, London (UCL).

Our technology platforms are available for both clinical usage and research collaboration. Click here to learn how we can work together.

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