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The images I am working with is a 3D sample imaged by cyto-DAPI. Individual cells were clearly visible in both moving and fixed images. We wanted to match those cells from two imaging rounds.
I have a question about the first step of the registration -- global RANSAC affine. I often get “insufficient fixed spots found”. To deal with it,
- shall I tweak the “blob_sizes” to get more spots? By reading your code, that seems to be the only parameter that controls how many blobs were detected.
- should the “blob_sizes” set to be the number of voxels spanned by half the size of a cell (radius)?
- what would be a good range of “blob_sizes”? I am using “s4 resolution - 1.89,1.84,1.84 um spacing (pre-expansion)”.
Any suggestions / directions would be appreciated.
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