Big data in nanoscale connectomics, and the greed for training labels.

The neurosciences have developed methods that outpace most other biomedical fields in terms of acquired bytes. We review how the information content and analysis challenge of such data indicates that electron microscopy (EM)-based connectomics is an especially hard problem. Here, as in many other current machine learning applications, the need for excessive amounts of labelled data while utilizing only a small fraction of available raw image data for algorithm training illustrates the still fundamental gap between artificial and biological intelligence. Substantial improvements of label and energy efficiency in machine learning may be required to address the formidable challenge of acquiring the nanoscale connectome of a human brain.

Dense connectomic reconstruction in layer 4 of the somatosensory cortex.

The dense circuit structure of mammalian cerebral cortex is still unknown. With developments in three-dimensional electron microscopy, the imaging of sizable volumes of neuropil has become possible, but dense reconstruction of connectomes is the limiting step. We reconstructed a volume of ~500,000 cubic micrometers from layer 4 of mouse barrel cortex, ~300 times larger than previous dense reconstructions from the mammalian cerebral cortex. The connectomic data allowed the extraction of inhibitory and excitatory neuron subtypes that were not predictable from geometric information. We quantified connectomic imprints consistent with Hebbian synaptic weight adaptation, which yielded upper bounds for the fraction of the circuit consistent with saturated long-term potentiation. These data establish an approach for the locally dense connectomic phenotyping of neuronal circuitry in the mammalian cortex.

SynEM, automated synapse detection for connectomics.

Nerve tissue contains a high density of chemical synapses, about 1 per µm3 in the mammalian cerebral cortex. Thus, even for small blocks of nerve tissue, dense connectomic mapping requires the identification of millions to billions of synapses. While the focus of connectomic data analysis has been on neurite reconstruction, synapse detection becomes limiting when datasets grow in size and dense mapping is required. Here, we report SynEM, a method for automated detection of synapses from conventionally en-bloc stained 3D electron microscopy image stacks. The approach is based on a segmentation of the image data and focuses on classifying borders between neuronal processes as synaptic or non-synaptic. SynEM yields 97% precision and recall in binary cortical connectomes with no user interaction. It scales to large volumes of cortical neuropil, plausibly even whole-brain datasets. SynEM removes the burden of manual synapse annotation for large densely mapped connectomes.