Typicality: | 0.457 |
Saliency: | 0.486 |
for one snp | 2 | purpose |
chromosome → be used in → variant calling | 9 |
chromosome → be → variant | 3 |
negative | neutral | positive |
0.248 | 0.729 | 0.023 |
Raw frequency | 12 |
Normalized frequency | 0.486 |
Modifier score | 0.500 |
Perplexity | 114.546 |