In this work, we tackle the problems of efficiency and scalability for predictive coding networks in machine learning. To do so, we first propose a library called PCX, whose focus lies on performance and simplicity, and provides a user-friendly, deep-learning oriented interface. Second, we use PCX to implement a large set of benchmarks for the community to use for their experiments. As most works propose their own tasks and architectures, do not compare one against each other, and focus on small-scale tasks, a simple and fast open-source library adopted by the whole community would address all of these concerns. Third, we perform extensive benchmarks using multiple algorithms, setting new state-of-the-art results in multiple tasks and datasets, as well as highlighting limitations inherent to PC that should be addressed. Thanks to the efficiency of PCX, we are able to analyze larger architectures than commonly used, providing baselines to galvanize community efforts towards one of the main open problems in the field: scalability. The code for PCX is available at https://github.com/liukidar/pcax.

Forming accurate memory of sequential stimuli is a fundamental function of biological agents. However, the computational mechanism underlying sequential memory in the brain remains unclear. Inspired by neuroscience theories and recent successes in applying predictive coding (PC) to \emph{static} memory tasks, in this work we propose a novel PC-based model for \emph{sequential} memory, called \emph{temporal predictive coding} (tPC). We show that our tPC models can memorize and retrieve sequential inputs accurately with a biologically plausible neural implementation. Importantly, our analytical study reveals that tPC can be viewed as a classical Asymmetric Hopfield Network (AHN) with an implicit statistical whitening process, which leads to more stable performance in sequential memory tasks of structured inputs. Moreover, we find that tPC exhibits properties consistent with behavioral observations and theories in neuroscience, thereby strengthening its biological relevance. Our work establishes a possible computational mechanism underlying sequential memory in the brain that can also be theoretically interpreted using existing memory model frameworks.