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dc.contributor.authorYADAV, SHASHI BALA-
dc.date.accessioned2022-07-28T09:43:31Z-
dc.date.available2022-07-28T09:43:31Z-
dc.date.issued2022-05-
dc.identifier.urihttp://dspace.dtu.ac.in:8080/jspui/handle/repository/19284-
dc.description.abstractEvery year there are almost 2-3 million deaths by latent tuberculosis persists in over a billion individuals worldwide. It is being very clear that TB is spread through the air when people with lung TB cough, sneeze, or spit. A person needs to inhale only a few germs to become infected. As a result, there is an essential need for an innovative approach to tuberculosis treatment. During chronic infection with M. tuberculosis, or early innate immune response the phagocytes initiate internalization of M. tuberculosis through the pathogenic antigen. Phytochemicals,which are plant-derived metabolites that act as anti mycobacterial are used in a wide variety of medical applications. In this work, we applied computational techniques to evaluate the therapeutic potential of diverse plant phytochemicals that can be used against diabetes, as well as the control of differentially expressed genes via molecular pathways and biological processes which will aid in tuberculosis management. We analyzed a RNA seq dataset for diabetes taken from the GEO database and further processed it as per requirementsinto an usable report. A total of 379 genes were identified out of which 16 were getting upregulated and 363 downregulated genes. These genes were then matched with the phytochemicals from the plants that are known to have an effect for diabetes. Later on, gene enrichment analysis revealed that the downregulated DEGs were mainly enriched in the biological processes like regulation of apoptotic signalling, mitochondrial depolarisation and in Angiotensin Activated Signalling. Upregulated DEGs were basically related to the biological process like cellular responsesto organic cyclic compounds. Finally, hub genes and hub modules were identified that could show a potential significance in the Diabetesen_US
dc.language.isoenen_US
dc.relation.ispartofseriesTD-5839;-
dc.subjectDECIPHERING PATHWAYSen_US
dc.subjectTUBERCULOSISen_US
dc.subjectGENE EXPRESSION ANALYSISen_US
dc.subjectDEGsen_US
dc.titleDECIPHERING PATHWAYS ASSOCIATED WITH TUBERCULOSIS USING GENE EXPRESSION ANALYSISen_US
dc.typeThesisen_US
Appears in Collections:M.E./M.Tech. Bio Tech

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