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Misc updates/fixes #15

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30 of 37 tasks
onursumer opened this issue Sep 26, 2019 · 1 comment
Open
30 of 37 tasks

Misc updates/fixes #15

onursumer opened this issue Sep 26, 2019 · 1 comment
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@onursumer
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onursumer commented Sep 26, 2019

Home Page:

  • Blurb (further detailed in about) (Slack Barry or Mike): needs text. Method, Assay, Glossary, etc
  • Change the blurb on front page from using bold to highlight the letters in the words that form the acronym to use underline instead
  • Table: expandable table switch columns (order: pathogenic germline, biallelic, somatic mutant)
  • 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)
  • For freqs put - instead of 0 (0 out of 0)
  • % somatic mutant -> % somatic driver, % pathongeic germline -> % germline pathogenic
  • 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?
@jjgao
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jjgao commented Oct 2, 2019

updated checklist based on feedback from lab meeting.

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