From: Jon M. <jon...@mo...> - 2005-03-31 13:32:46
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On Wed, 2005-03-30 at 21:10, Gordon Kindlmann wrote: > Fixing bane has been on my todo list > for so long its sad. It wouldn't be that hard. But, if you're a real > masochist, you can get the guidance from value/gradient scatterplots > created via vprobe and then "unu jhisto", and then based on these you > can use "gkms txf" to make transfer functions. I can give you some > more pointers on this if you're interested (ask again on teem-users). > I have some hack to get gkms to compile even though bane is messed- the > "txf" command is actually independent of bane so it works. This is > then something you can feed into miter. Yes I'd like to try it out, so let me know how your work-around works. > One thing to keep in mind is that if you have a lot of > datasets of the same modality, collected with the same parameters, of > the same kind of specimen (common in science), one txf may work for > them all, which lessens the needs to do clever semi-automatic transfer > functions. This is largely true, but with biological (in vivo) systems the variability across subjects can be surprisingly high even when modality and acquisition parameters are identical. -- Jon |