To fill in my profile tags, a thread:
#TrakEM2 is open source software mostly for #connectomics (but found uses well beyond), and provides the means for both manual and automatic montaging and aligning overlapping 2D image tiles (with #SIFT features and rigid or elastic transformation models), and then reconstructing with mostly manual means–by painting with a digital brush–the volumes of structures of interest, as well as trace the branched arbors of e.g., neurons and annotate their synapses, therefore mapping a #connectome from #vEM (volume electron microscopy).
#TrakEM2 paper at https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0038011
Git repository at https://github.com/trakem2/
For 3D visualization, #TrakEM2 uses the 3D Viewer https://imagej.net/plugins/3d-viewer/
As software, #TrakEM2 runs as a plugin of #FijiSc https://fiji.sc/ and in fact motivated the creation of the #FijiSc software in the first place, to manage its many dependencies and therefore facilitate distribution to the broader #neuroscience community.
#TrakEM2 was founded in 2005, when terabyte-sized datasets were rare and considered large. The largest dataset that I've successfully managed with #TrakEM2 was about 16 TB. For larger datasets, see #CATMAID below.
For an introduction to #FijiSc from the comfort of #python (or rather, #jython 2.7), see my online tutorial, walking you through image processing concepts with working code that you can copy-paste into the Script Editor, which has code autocompletion to facilitate class and method discovery across the many libraries: https://syn.mrc-lmb.cam.ac.uk/acardona/fiji-tutorial/