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Once the maximum on the saliency map is detected, we initialize an active contour on this position; see Figure 5. Then after convergence of the snake, we obtain the segmentation of the object displayed in Figures 6 and 7.
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Then, small abnormal regions in the modulation map were detected by high speed local contrast method and defined as candidate targets.
Inference was aided by GraphPad InStat (version 3.00, GraphPad Software, Inc., San Diego, CA, USA) MAP DNA was amplified from the blood of 33 out of 59 T1DM patients (55.9%) whereas MAP was detected only in 18 out of 79 healthy controls (22.7%) indicating a statistically highly significant difference (Table 1).
Minimal responses were seen in patients with inactive disease and in non-IBD patients while the results from CD patients with active disease are summarized in Table 2. T-cell lines that reacted to MAP were detected in 5 of 7 (71%) patients in the CD group.
Mitochondria were detected with Mitotracker (red) and Map was detected with anti-myc (green).
MAP was detected in those from Angola and South Africa, and the yogurt from South Africa also showed Brucella.
By culture, MAP was detected in 62 of the 445 fecal pools (13.9%).
Using F57 real-time PCR, MAP was detected directly in 9 of the 445 pools (2.0%).
By culture, MAP was detected in fecal samples of all 17 animals.
No obvious correlations between seed weight and regions of the linkage map were detected.
The same LD map was detected in control group when comparing with CHB population in Hapmap database (r =0.842).
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