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Table 4 Multi-location prediction results on the PROSITE-GO version of the dataset, per location, averaged over 25 runs of 5-fold cross-validation, for the combined set of single- and multi-localized proteins

From: Protein (multi-)location prediction: using location inter-dependencies in a probabilistic framework

 

cyt (3785)

ex (1405)

nuc (2952)

mem (1824)

mi (870)

Pre- Std s i (SVMs)

0.84 (± 0.01)

0.87 (± 0.02)

0.79 (± 0.02)

0.93 (± 0.01)

0.90 (± 0.03)

Pre- Std s i (Our system)

0.84 (± 0.01)

0.91 (± 0.02)

0.79 (± 0.03)

0.90 (± 0.01)

0.87 (± 0.03)

Rec- Std s i (SVMs)

0.85 (± 0.01)

0.64 (± 0.02)

0.72 (± 0.02)

0.79 (± 0.02)

0.62 (± 0.03)

Rec- Std s i (Our system)

0.86 (± 0.01)

0.65 (± 0.02)

0.74 (± 0.03)

0.80 (± 0.02)

0.66 (± 0.03)

Pre s i (SVMs)

0.82 (± 0.01)

0.89 (± 0.02)

0.83 (± 0.01)

0.92 (± 0.01)

0.87 (± 0.03)

Pre s i (Our system)

0.81 (± 0.02)

0.91 (± 0.02)

0.83 (± 0.01)

0.90 (± 0.01)

0.89 (± 0.02)

Rec s i (SVMs)

0.78 (± 0.01)

0.72 (± 0.02)

0.77 (± 0.01)

0.76 (± 0.01)

0.68 (± 0.02)

Rec s i (Our system)

0.80 (± 0.01)

0.74 (± 0.02)

0.78 (± 0.02)

0.78 (± 0.01)

0.73 (± 0.02)

  1. Results are shown for the five locations s i that have the largest number of associated proteins (the number of proteins per location is given in parenthesis): cytoplasm (cyt), extracellular space (ex), nucleus (nuc), membrane (mem), and mitochondrion (mi). The table shows the per-location measures: standard precision (Pre- Std s i ), recall (Rec- Std s i ), Multilabel-Precision ( Pre s i ), and Multilabel-Recall ( Rec s i ), obtained from SVMs without using location inter-dependencies and from our system using location inter-dependencies. For each location and measure, the highest of the values obtained from the two methods is shown in boldface. Standard deviations are shown in parentheses.