Understanding how neural circuits integrate sensory and state information to support context-dependent behavior is a central issue in neuroscience. In Drosophila, oviposition is a complex process in which the fly integrates context and sensory information to choose an optimal location to lay her eggs. The circuit that controls the oviposition sequence is known, but how the circuit integrates multiple sensory modalities and internal states is not. We investigated the neural circuitry underlying high-level processing related to oviposition using the Hemibrain connectome. We identified the Oviposition Inhibitory Neuron (oviIN) as a key hub in the oviposition circuit and analyzed its inputs to uncover potential parallel pathways that may be responsible for computations related to high-level decision-making. We applied graph-theoretic analyses on the sub-connectome of inputs to the oviIN to identify modules of neurons that may constitute novel circuits. Our findings indicate that the inputs to oviIN form multiple parallel pathways from the unstructured neuropils of the Superior Protocerebrum where high-level computations have been known to occur.