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Mohsen Sojoudi

Rare Diseases Foundation of Iran, Iran 

Title: Future heredity of rare diseases and orphan drugs

Biography

Biography: Mohsen Sojoudi

Abstract

Nowadays through continuous progression, the necessity of data analysis on the diagnosis of rare out of non-rare diseases through providing connections among worldwide statistical scientific discoveries is felt. Bioinformatics resources and database tools about the genetic disorders, useful management of sample sequences and post-transcriptional regulation could be the starting point for solving the difficulties on the identification of rare diseases. Making a right and timely diagnosis is coming to be a significant difficulty for rare diseases delayed diagnosis. Rare diseases patients’ analytic data management and its trending may pave the way of their future and lifestyle. Rare diseases trending is quite various through geographical borders and requires expertise and systematic data management. To achieve the applied software techniques, the social challenges as well as clinical research studies seems to be the most important. Later on, the internet and electronic healthcare and telemedicine systems, portal and software are quite applicable and useful. The analytic databases must be included OMICS (genomics, proteomics and metabolomics), the experimental data browsed through software designation. The access to a wide range of biological data plays the first role in bioinformatics and relevant database as the organized set of information and research studies in laboratories and revision of analytic scientific publications consisting of structured and organized entries at their both availability and easy application. This article indicates the principles for the scientific data analysis as to be findable, accessible and innovatively reusable to practically improve the diagnosis of rare diseases throughout the world specially the developing countries.