Dear developers and users of ImageJ,
Currently in our department we are trying to find a standardized method of
tracing neurons received from stacks. We generate the stacks and any
substacks within Fiji and once we have a target neuron we import the stacks
into Neuronstudio to trace it, as Neuronstudio can automatically trace.
After saving these traces in an swc file we try to reload it into Fiji
Simple Neurite tracer, however we always encounter an issue with scaling.
We always have the correct offset coordinates at hand, previously saved
from the original stacks in Fiji, but the offset scaling is always off,
sometimes really off. The tracings always appear smaller than the original.
With trial and error we can come as close as possible to the correct
scaling but this is rather time consuming and the endgoal is to fully
automate the whole process via standard procedures for a protocol, that
will be used in the lab. Would anybody know if what the precise error is or
how to work around it?
With kind regards,
Concerned Master internees
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