PRISMΔDB

Analyze how specific documents activate the features of the SAE. Select a dataset, a run and a document to begin.

Active Features

1521

0.0
Details List
#2944 Feature 2944
2.9
#2335 Feature 2335
2.5
#2998 Feature 2998
2.5
#1159 Feature 1159
2.4
#1674 Feature 1674
2.3
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2.3
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2.3
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2.2
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2.2
#170 Feature 170
2.2
#2005 Feature 2005
2.1
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2.1
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2.0
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2.0
#464 Feature 464
2.0
#1225 Feature 1225
1.9
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1.9
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1.9
#2338 Feature 2338
1.9
#1615 Feature 1615
1.8
#30 Feature 30
1.8
#828 Feature 828
1.8
#681 Feature 681
1.7
#418 Feature 418
1.7
#1891 Feature 1891
1.7
#239 Feature 239
1.6
#2382 Feature 2382
1.6
#1930 Feature 1930
1.6
#1494 Feature 1494
1.6
#1774 Feature 1774
1.6
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1.6
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1.5
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1.5
#705 Feature 705
1.5
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1.5
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1.5
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1.5
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1.4
#0 Feature 0
1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
#433 Feature 433
1.3
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1.3
#1848 Feature 1848
1.3
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1.3
#1925 Feature 1925
1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
#357 Feature 357
1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
#375 Feature 375
1.2
#94 Feature 94
1.2
#2016 Feature 2016
1.2
#293 Feature 293
1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.0
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1.0
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1.0
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1.0
#1465 Feature 1465
1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
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1.0
#155 Feature 155
1.0
#3004 Feature 3004
1.0
#2325 Feature 2325
1.0
#331 Feature 331
1.0
#728 Feature 728
1.0
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1.0
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1.0
#330 Feature 330
0.9
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0.9
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0.9
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0.9
#1428 Feature 1428
0.9
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0.9
#134 Feature 134
0.9
#1577 Feature 1577
0.9
#1901 Feature 1901
0.9
#101 Feature 101
0.9
#1154 Feature 1154
0.9
#2825 Feature 2825
0.9
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0.9
#1269 Feature 1269
0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
#2853 Feature 2853
0.9
#1522 Feature 1522
0.9
#1463 Feature 1463
0.9
#1646 Feature 1646
0.9
#3032 Feature 3032
0.9
#1710 Feature 1710
0.9
#660 Feature 660
0.9
#2714 Feature 2714
0.9
#3040 Feature 3040
0.9
#1050 Feature 1050
0.9
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0.9
#2946 Feature 2946
0.9
#1098 Feature 1098
0.9
#1746 Feature 1746
0.9
#1543 Feature 1543
0.9
#2740 Feature 2740
0.9
#15 Feature 15
0.9
#148 Feature 148
0.9
#1427 Feature 1427
0.9
#2102 Feature 2102
0.9
#1012 Feature 1012
0.9
#2032 Feature 2032
0.9
#888 Feature 888
0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
#41 Feature 41
0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
#21 Feature 21
0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.6
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0.6
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Document Content

Gas-chromatographic screening of capsular polysaccharides of Neisseria meningitidis.
Thirteen systemic strains, i e strains isolated from systemic infections, and 77 carrier isolates of Neisseria meningitidis were serogrouped by agglutination and analyzed by gas chromatography (GC) of phenol extracts. For systemic strains the sugar patterns were in accordance with their group-specific capsular polysaccharides (CPS). Some carrier isolates revealed unexpected GC profiles. Upon immunological retesting with new sera, GC results were generally confirmed. Occasional isolates initially serogrouped as B or Y completely lacked neuraminic acid. Some non-groupable isolates were shown by ultracentrifugation and GC to have significant amounts of this sugar likely to originate from CPS of known composition or from unknown polysaccharides. One such originally non-groupable isolate showed a weak agglutination reaction specifically with group B antiserum when reexamined. Generally, carrier isolates had lower amounts of CPS than systemic strains of the same group. Five successive isolates from one carrier were first serogrouped as X, Z or non-groupable, but they had high amounts of galactosamine and 2-keto-3-deoxy octonate, sugars characterizing CPS of serogroup 29E. These isolates were confirmed by agglutination with recently available group 29E antiserum to be of this serogroup, which has not been reported before in Norway. Ultracentrifugation revealed the presence of unknown polysaccharides containing glucose, galactose or glucosamine, but further purification of these polymers is required to determine their composition and immunological importance.