Conceptualizing the Need of Computer Aided Technologies for Molecular Diagnostics of Mutational Genes: A Review

In the current era scenario where, human intelligence is challenged by a virtual computer by the process of artificial intelligence, this further aims to assist humans in all scenarios. Molecular diagnostics of diseases is considered as vital science for accurate diagnose of ailment and further to subject precise medicine. Analysis of 10,000 molecules by human brain takes days of experimental modelling and response collections whereas this task is made easy by a click of software and group of algorithms. The study in the present paper aims to understand and conceptualize the dependency of computational systems in medical science which are not only assisting physicians to store and visualize disease information but also now predicting the responses with complete diagnose report. The review majorly focusses on blood carrier hemoglobin deficiency in humans and autosomal linked cri-du chat syndrome in infants. Space anaemia is a phenomenon that raises important issues about the fundamental mechanisms governing erythropoiesis under such harsh settings. The goal of the current study is to clarify the spatiotemporal expression and regulation of haemoglobin in space by utilizing multi-omics techniques to examine data from multiple space missions. Cri du Chat syndrome is a complex hereditary disorder that highlights the need for continued research as well as care for afflicted individuals and their families. The review paper further highlights the key role of computer algorithm used in modern medicine era for early diagnosis and population statistics.