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Table: add penetrance and sort by penetrance (sort by highest level of penetrance if the gene is in multiple penetrance groups) sort by % Germline Biallelic
Table: search by gene symbol only
“Includes only likely driver mutations, or relevant copy number changes”
Mouse over any frequency should show nominator + denominator
Include all cancer types in expandable row (including zero)
When row is expanded, remove row header Mutation frequencies etc
What should tooltip be for biallelic %?
Fetching INSIGHT(ful) mutations
Left justify insight logo, right justify mskcc
Hide sub table on search
arrow not in the right spot for tooltip
Percent of pathogenic germline carriers biallelic in the corresponding tumor -> Percent of pathogenic germline carriers biallelic in the corresponding tumor sample
Somatic
Move total # Samples to front in expanded table
Gene Page:
Benign germline -> Rare Benign/VUS germline (less than 2% of the whole cohort?)
Start y axis from 1 when using numbers
Add some space for lollipops to show lines
Y-Axis: Radio-button
Benign + pathogenic germline different color in table
Somatic row show - in biallelic
Justify headers same as content
Add cDNA change column (hgvsc from genome nexus)
Variable number of decimal point digits in the tooltip (currently fixed to 4 digits)
move the + sign (expander) at the end to % column on gene page
make y and -y same scale (round up digits on ticks (no need for two digits))
tool tip for Rare Benign/VUS Germline isn't precisely accurate
when hover over (i) next to gnomAD/ClinVar column header, the cursor does not change to hand icon but rather to a column resizing icon
About Page:
The citation in the About page should be updated to correct the title and its status.
Download Page
link to github repos
accession codes to paper
Data
penetrance
what defines a rare benign germline?
The text was updated successfully, but these errors were encountered:
Home Page:
sort by penetrance (sort by highest level of penetrance if the gene is in multiple penetrance groups)sort by% Germline Biallelic
-
instead of 0 (0 out of 0)Gene Page:
-
in biallelicRare Benign/VUS Germline
isn't precisely accurate(i)
next to gnomAD/ClinVar column header, the cursor does not change to hand icon but rather to a column resizing iconAbout Page:
Download Page
Data
The text was updated successfully, but these errors were encountered: