This may be helpful for you:
http://bigwww.epfl.ch/thevenaz/stackreg/Best regards,
John
On 25 sept. 2012, at 12:39, 中村 宗一 wrote:
> I took tiff images of serial slices of a cell with a confocal microscope and stacked them and made a 3d projection. But I found that the cell moved slightly at random during taking tiff images. Please help me how to adjust the cell position between tiff images.
>
> Na
>
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