used Python to analyze human promoter sequences and select candidates that have a high G-quadruplex formation potentialused physico-chemical analysis such as isothermal titration calorimetry (ITC), ultraviolet–visible spectroscopy (UV-Vis) and circular dichroism spectroscopy (CD) to study the dynamics of G-quadruplex formation for selected sequences and a series of mutated sequences

The goal of the project was to observe the mislocalization of polarity marker proteins in the fly lines with a specific mutation using confocal microscopy.