Difference between revisions of "Distribution modeling"
From NAMIC Wiki
Line 2: | Line 2: | ||
<gallery> | <gallery> | ||
Image:PW-2015SLC.png|[[2015_Winter_Project_Week#Projects|Projects List]] | Image:PW-2015SLC.png|[[2015_Winter_Project_Week#Projects|Projects List]] | ||
+ | Image:Genu_fa_3d_conte_vs_krabbe.png | ||
+ | Image:Neo_Avg_leave1out_CDF.png | ||
+ | Image:Neo_AvgCurves_leave1out_CDF.png | ||
+ | Image:Neo_DIST_leave1out_CDF.png | ||
</gallery> | </gallery> | ||
+ | |||
+ | |||
==Key Investigators== | ==Key Investigators== |
Revision as of 15:35, 9 January 2015
Home < Distribution modeling
Key Investigators
Anuja Sharma, Guido Gerig
Project Description
Objective
- Evaluate the ability of regression methods utilizing distribution-valued measurements to differentiate between healthy controls and patients with pathology.
Approach, Plan
- Model probability distributions along DTI fiber tracts instead of scalar summary measurements to create a tract profile (e.g. cross-sectional averages).
- Our spatiotemporal modeling method utilizes these distribution-valued data to create growth trajectories such that the complete probability distribution is estimated continuously in space and time.
- Using these methods, we can estimate a spatiotemporal growth trajectory for the healthy infant population. We then compare our method's ability to detect clinical differences in infants with Krabbe's disease in reference to a control population.
Progress
- We found that our method had better sensitivity towards finding differences in growth trajectories.
- We could find statistically significant differences in scenarios where the differences were small enough to be missed by conventional methods.