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Advanced Normalization Tools (ANTs)
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AntsRegistration #1611

Closed tarasepehri closed 10 months ago

tarasepehri commented 1 year ago

Hello experts,

I am a newbie and I am struggling in registering lamb brains to a template. The images belong to neonate lambs and the template belong to sheep brain. I used AntsRegistrationSynQuick, followed by AntsRegistrationSyn. I tried SynQuick alone, it's close but not great, both registration one after the other is not good too. I tried moving template, as well as moving the image. none gives a good result. Could anyone please kindly help me solving this puzzle? I attached the template and a T1. T1 is denoised, bias corrected and in the same orientation as the template. TSBTA_Mixed_Brain_new1-template.nii.gz T1-28NL.nii.gz

ntustison commented 1 year ago

Thanks for posting the images.

I don't know what you expect here but even just looking at the images, there doesn't appear to be an obvious dense correspondence. Is the template constructed from the same modality as the single subject?

tarasepehri commented 1 year ago

Thanks for your response. The template and the lamb brain are both MRI and T1-W. However, The T1-28NL belongs to neonate lamb. So it doesn't have as clear WM, GM structures. But in coregistration, even the ventricles don't align. They both have clear ventricles structure. I tried antsRegistration with T2 images as well which has better correspondence. But it didn't work. T2toT1-28NL-masked.nii.gz

ntustison commented 1 year ago

But in coregistration, even the ventricles don't align. They both have clear ventricles structure

This might be true but other correspondence ambiguities might contribute to an overall poor registration.

In addition to the images, please provide the command call so that we can reproduce your results on our end.

tarasepehri commented 1 year ago

I appreciate your help. I use the default command. antsRegistrationSynQuick.sh -d 3 -f T2toT1-28NL-masked.nii.gz -m TSBTA_Mixed_Brain_new1-template.nii.gz -o templatetoT2-SynQ -n 4 then antsRegistrationSyn.sh -d 3 -f T2toT1-28NL-masked.nii.gz -m templatetoT2-SynQWarped.nii.gz -o templatetoT2-SynQtoT2 -n 4 Tried those for both T1 and T2 images. I understand that there would be poor registration in most regions. If I can get a good registration for wm region around ventricles like Hippocampus, Thalamus, Cerebellum, Corpus Callosum, Internal Capsu I'll be happy.

Attached is the labels. TSBTA_Brain_Altas.nii.gz

Thanks so much.

ntustison commented 1 year ago

Yeah, with these data, it might be too much to ask to get good alignment for all those structures based on intensity alone. You might actually have to provide subject labelings for the structures.

tarasepehri commented 1 year ago

Could you please let me know how can I do that? How can I improve the coregistration?

On Thu, 19 Oct 2023, 1:26 pm Nick Tustison, @.***> wrote:

Yeah, with these data, it might be too much to ask to get good alignment for all those structures based on intensity alone. You might actually have to provide subject labelings for the structures.

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cookpa commented 1 year ago

If antsRegistrationSynQuick.sh appears to be working reasonably, it might be because it uses the Mattes metric. In general we don't recommend this for SyN intra-modality, but because you have quite different contrasts, it might be better.

Both of the scripts will print a registration command, which you can edit. The quick script uses Mattes but doesn't do many iterations at high resolution. You can try editing it to further refine the output.