|
|
|
|
|
by sxg
1717 days ago
|
|
Hey! I actually handled the data coordination for the BraTS data sets. We used a combination of the best algorithms from prior years of the BraTS competition to pre-segment the data sets, and then we had experts (fully-trained neuroradiologists) make manual corrections, which were then further reviewed by my team before finalization. The three tissue types of interest are fairly easy to identify in most cases. Edema is bright on the FLAIR sequence, enhancing tumor is bright on T1 post-contrast and dark on pre-contrast, and necrosis is relatively dark on T1 pre- and post-contrast while also being surrounded by enhancing tumor. These rules hold true in most cases, so it’s really just a matter of having the algorithm find these simple patterns. The challenge in doing this manually is the amount of time it takes to create a really high quality 3D segmentation. It’s painful and very tough to do with just a mouse and 3 orthogonal planes to work with. |
|