Signal Next Iteration

[inodb]

Data

• Address other/unkown cancer types (https://www.signaldb.org/variant/13:g.32914438_32914438delT
• Show total biallelic ratio for Benign/VUS (needs to discuss with Chai)

Visual

• Show icon for internal SIGNAL data or icon for external sources
• Rename Annotation -> Somatic Annotation. Remove annotations for germline (except civic)
• Rename ClinvarID -> Clinvar. Use clinvar description instead of ID. (Maybe we can make the id available for download)
• show both pathogenic germline and somatic by default. Show germline mutations in table on top (sort by germline) Moved to Gene page improvements #66
• on explore page make it more clear in tooltip what variants you're navigating to. Maybe list number behind it. Could also add links for pathogenic germline and bialellic.
• Update %Biallelic header tooltip description to Percent of germline carriers biallelic in the corresponding tumor sample (if we decide to show total biallelic ratio for Benign/VUS)
• in gene page, style HGVSg (e.g. underlining) to make it more obvious that it’s a hyperlink.
• Hiding additional columns (Age at dx etc...) until we get new data for pathogenic variants

URL

• make gene uppercase: https://www.signaldb.org/gene/tp53
• link the gene name on variant page to the gene page

Analytics

• Add google analytics