PhD (Medical Genetics)
2019-2023
Embarking on a journey in pursuit of a Ph.D. in Medical Genetics with a focus on rare genetic disorders is a testament to my passion for unraveling the intricacies of the human genome. In this dynamic and ever-evolving field, I am driven by the profound impact that understanding rare genetic disorders can have on individuals and families facing these challenges. My research endeavors are dedicated to advancing knowledge in medical genetics, particularly honing in on the rarest and most elusive genetic anomalies. Through rigorous academic inquiry and hands-on laboratory experiences, I am committed to contributing valuable insights that may pave the way for innovative diagnostic approaches, therapeutic interventions, and ultimately, improved patient outcomes. My personal website serves as a digital canvas, showcasing the milestones of this academic odyssey and the profound societal implications of unraveling the mysteries encoded within our DNA. Join me on this transformative journey as we explore the frontiers of medical genetics, seeking to make a tangible difference in the lives of those affected by rare genetic disorders.
Certificate course in Biostatistics, Epidemiology and Research Methodology
03.2020
Bachelor of Dental Surgery (BDS)
2013-2018
I have done my Bachelors in Dentisty.
Junior Research Fellow
2018-2019
As a professional in the field of DNA sequencing and laboratory management, my expertise encompasses a range of crucial responsibilities. These include Illumina DNA library preparation, managing sample inventory, tracking, and library planning. I also coordinate laboratory activities within my team, ensuring smooth operations. Additionally, I perform qualitative and quantitative analysis of nucleic acid using advanced instruments such as Nanodrop and Qubit. I excel in library preparation using the Illumina DNA PCR free protocol, employing both manual and automated processes with the Tecan freedom evo and Opentrons OT-2 systems. Furthermore, I am proficient in setting up and maintaining the NovaSeq 6000 sequencer, handling reagent cartridges and flowcells, and loading samples for sequencing. I also conduct thorough qualitative and quantitative analysis of the generated sequence data. Finally, I contribute to sample sheet preparation and collaborate with the bioinformatics team for seamless data analysis and interpretation.