Convert from Tracks
Tracks are useful for comparative analysis and visualization, but sometimes it is necessary to convert a track to a normal sequence or mapping. This can be done with the Convert from Tracks tool that can be found here:
Toolbox | Track Tools () | Track Conversion () | Convert from Tracks ()
One or more tracks can be used as input. In the example given in figure 24.18 a reads track and two annotation tracks are converted simultaneously to an annotated read mapping (figure 24.19).
Figure 24.18: A reads track and two annotation tracks are converted from track format to stand-alone format.
Figure 24.19: The upper part of the figure shows the three individual input tracks, arranged for simplicity in a track list. The lower part of the figure shows the resulting stand-alone annotated read mapping.
Likewise it is possible to create an annotated, stand-alone reference from a reference track and the desired number of annotation tracks. This is shown in figure 24.20 where one reference and two annotation tracks are used as input.
Figure 24.20: A reference track and two annotation tracks are converted from track format to stand-alone format.
The output is shown in figure 24.21. The reference sequence has been transformed to stand-alone format with the two annotations "CDS" and "Gene".
Figure 24.21: The upper part of the figure shows the three input tracks, shown for simplicity in a track list. The lower part of the figure shows the resulting stand-alone annotated reference sequence.
Depending on the input provided, the tool will create one of the following types of output:
- Sequence ()
- Will be created when a sequence track () with a genome with only one sequence (one chromosome) is provided as input
- Sequence list ()
- Will be created when a sequence track () with a genome with several sequences (several chromosomes) is provided as input
- Mapping ()
- Will be created when a reads track () with a genome with only one sequence (one chromosome) is provided as input.
- Mapping table ()
- Will be created when a reads track () with a genome with several sequences (several chromosomes) is provided as input.