Single cell labeling allows identification of neuron types based on neurite trajectories, an essential step to understand
brain anatomy and function. For years, various techniques have been developed to achieve in vivo single cell labeling. In
Drosophila
, several genetic mosaic approaches have not only allowed labeling of specific neuron subsets but also enabled manipulations
of gene function or neural activity in or outside the marked cell(s). They collectively provide an unprecedented level of
versatility for diverse targeted studies. In this chapter, we selectively cover the general methods of single neuron labeling
mediated by flip-out or mitotic recombination.