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The nih-ms-mp2rage dataset contains UNIT1-denoised data and T1-maps (see #280 (comment) ), however for MS lesion segmentation UNIT1 non-denoised is classically used (and it is the contrast that we have for the other MS MP2RAGE datasets: marseille-3T-mp2rage and basel-mp2rage),
so a strategy is required to be able to synthesize UNIT1 non-denoised images from the T1-maps.
UNI-den
T1-map
Strategy:
The synthesis of UNI images from T1maps was reported in the work of Massire et al., 2021
For this synthesis, some MP2RAGE acquisition parameters are required such as : nbefore, nafter, alpha1, alpha2, TR, MP2RAGE-TR, TI1 and TI2. Parameters not available for the nih-ms-mp2rage data,
but if I take the parameters reported by Demortière et al., 2020
I obtain the following results:
Synthetic UNI from non-den T1-map
I believe that we would have more precise results if we have the MP2RAGE parameters from nih-ms-mp2rage data.
I'm not a fan of this two-step strategy-- what if the synthesis misses minor lesions? Why not train a model with den-UNI1 and non-denUNI1 first and see what you get?
Description
The
nih-ms-mp2rage
dataset containsUNIT1-denoised
data andT1-maps
(see #280 (comment) ), however for MS lesion segmentationUNIT1 non-denoised
is classically used (and it is the contrast that we have for the other MS MP2RAGE datasets:marseille-3T-mp2rage
andbasel-mp2rage
),so a strategy is required to be able to synthesize
UNIT1 non-denoised
images from theT1-maps
.UNI-den
T1-map
Strategy:
nbefore, nafter, alpha1, alpha2, TR, MP2RAGE-TR, TI1 and TI2
. Parameters not available for thenih-ms-mp2rage
data,but if I take the parameters reported by Demortière et al., 2020
I obtain the following results:
Synthetic UNI from non-den T1-map
I believe that we would have more precise results if we have the MP2RAGE parameters from
nih-ms-mp2rage
data.Related issues:
#280
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