Table 1.
Species | Global networks | Context-specific networks | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Databases | Literature | Binding site | ChIP | Open chromatin | |||||||
N | N | N | CO | AB | E | N | CO | E | N | N | |
Human | 4 | 4 | 12 | 103 | 192 | 1,206 | 1,206 | 105 | 248 | 3,617 | 4,843 |
Mouse | 2 | 4 | 12 | 28 | 50 | 162 | 162 | 39 | 123 | 1,800 | 1,980 |
Worm | 2 | 4 | 4 | 15 | 91 | 561 | 561 | — | — | – | 575 |
Fly | 3 | 4 | 22 | 23 | 59 | 119 | 119 | — | — | – | 148 |
11 | 16 | 54 | 169 | 392 | 2,048 | 2,048 | 144 | 371 | 5,417 | 7,546 |
Global networks and context-specific networks derived from the ENCODE data are integrated into the CroCo repository. Database derived networks stem from different curated sources (e.g., ORegAnno [39] and REDFly [40]). The binding site predicted networks result from different PWM collections and a sensitive and a specific PWM match threshold. Furthermore, four different global literature derived networks are included for each species. The majority of networks in the repository is inferred from context-specific ChIP and open chromatin experiments. In total, 2,048 networks derived from ChIP experiments performed for different antibodies and cell-lines are integrated into CroCo. Additionally, 5,417 networks derived from 371 open chromatin based experiments (e.g., DNase-seq and FAIRE-seq) are integrated into CroCo
N=Number of networks
CO=Number of different contexts (cell-lines for human, cell-lines or tissues for mouse, development stages for worm and fly)
AB=Number of different antibodies
E=Number of experiments