Table 2.
Category | Method | Operational model | Positive predictive value (%) | Note | Ref |
---|---|---|---|---|---|
Discriminative model | Heintzman’s method | Thresholds of histone modification profiles | 39.5 | Mapped to distal p300 binding sites in HeLa cells | [5] |
Visel’s method (2009) | Thresholds of p300 binding profiles | 87.7 | With reproducible enhancer activity in transgenic mouse | [46] | |
Narlikar’s method | Linear regression | 62 | With reproducible enhancer activity in vivo in mouse and zebrafish | [65] | |
Zinzen’s method | Support vector machine | 71.4 | With reproducible enhancer activity in transgenic Drosophila | [67] | |
Firpi’s method | Time-delay neural network | 66.3 | Overlapped with p300 binding sites, Dnase I hypersensitivity sites or TRAP220 binding sites in HeLa cells | [10] | |
Lee’s method | Support vector machine | 74.5 | Overlapped with Dnase I hypersensitive enhancers in embryonic mouse whole brain cells | [44] | |
ChromaGenSVM | Support vector machine | 57 | Overlapped with p300 binding sites, Dnase I hypersensitivity sites or TRAP220 binding sites in HeLa cells | [9] | |
Probabilistic graphical model | Won’s method | Hidden Markov model | 54.8 | Overlapped with p300 binding sites, Dnase I hypersensitivity sites or TRAP220 binding sites in HeLa cells | [11] |
Bonn’s method | Bayesian network | 78 | Overlapped with previously identified TF binding sites in Drosophila | [6] | |
Other | Chen’s method | Multinomial logistic | 83 | Overlapped with at least one TF peak from 7 mouse embryonic stem cell ChIP-seq datasets | [8] |
Yip’s method | Random forest | 67 | With enhancer activity in vivo in mouse and medaka fish (28/42) | [50] |
Note: The performance shown here is the reported performance compared to experimental results. The positive predictive value (percentage) was calculated as follows: positive predictive value = true positive/(true positive + false positive).