chromoscope
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Interactive multiscale visualization for structural variation in human genomes
Having shown GosCan to some people who haven't seen before, I have heard requests to add legends and remove abbreviations. In the linear view: CNV -> copy number variants LOH...
If a driver file does not include one of the optional attributes (according to documentation), the display shows "undefined", rather than a blank. More of a style issue, but of...
Supports a common analysis worfklow when users want to see the regions with driver mutations in detail.
Clicking a mutation or an indel in the linear view would trigger a .bam file display. This way, users will be able to assess evidence for each mutation too.
If Gosling already allows that, would be helpful to add the ability to show bases (in the read view) that are absent in reference genome. This makes it easy to...
https://googlegenomics.readthedocs.io/en/latest/use_cases/browse_genomic_data/igv.html
Example spec to test: https://gist.github.com/sehilyi/66a1091fc3766be1a76718bfaf79c491