A dataset is a group of files that are linked together in one category. Datasets could be arranged into hierarchy When NGB is opened, you will see a list of datasets in panel to the right
Grouped items could be expanded/collapsed, using an arrow icon next to a group name
Each item in the datasets hierarchy shows corresponding genome name (e.g. GRCh38, hg19. It is located to the right from the items name)
Each file item in the hierarchy shows its type (e.g. BAM, VCF, WIG, BED, etc.) to left from the file’s name
Data could opened by clicking a checkbox next to a dataset name (this will open all files, contained in a dataet) or next to a specific file
By default, you will see the following panels when you select files from datasets:
If no VCF files were selected, the Summary view will only show the list of loaded files.
If the one or more VCF files were selected, the Summary view will show the charts depicting the variations’ breakdown as follows:
Charts would show statistics on variations, according to selected filter.
This panel shows a table of variations retrieved from all loaded VCF files.
This panel shows a list of all files, loaded and visualized as tracks in the Browser panel.
Tick or untick a track in the Datasets panel to toggle its visibility.
You can view the loaded tracks as follows:
Depending on the selection type, you will see the visualizations as follows:
Each track has the following parts: