feat: render canonical transcript source

snakemake-workflows / dna-seq-varlociraptor

A Snakemake workflow for calling small and structural variants under any kind of scenario (tumor/normal, tumor/normal/relapse, germline, pedigree, populations) via the unified statistical model of Varlociraptor.

MIT License

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feat: render canonical transcript source #282

Closed FelixMoelder closed 2 months ago

FelixMoelder commented 5 months ago

In some rare cases multiple transcripts for the same variant show up in the datavzrd report. This happens in case the canonical and mane_plus_clinical fields state different transcripts as canonical. As we can not identify the correct one we added both entries to the datavzrd report in the detail view showing black cells for supporting transcripts. Additionally, a column for Enseml protein ID has been added.

FelixMoelder commented 2 months ago

These changes have already been merged in a previous PR.