Efficient graphical overview of variant scores

[xiamaz]

The number of bioinformatics scores for describing a variant can be very large. Gaining a quick overview of a larger number of scores can quickly become unwieldy, as adding additional columns does not properly scale and dropdowns can only be viewed one variant at a time.

I propose a set of small graphical indicators for individual variants:

The order of these should be fixed, based on the available scores. Sections can be added to properly differentiate different score types, such as missense, splicing and phenotypic scores.

special shapes could be utilized to highlight certain especially relevant scores:

On click, the detailed breakdown of individual score values should be shown.

[holtgrewe]

Will need worker-based filtration of seqvars.