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exploring proteins #97
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Overall, I feel that we already had this conversation, but with gene instead of protein ;) Nevertheless there are still some problems: the gene/browse page is terribly slow now. It wasn't the last time I was checking it out. I will investigate this; maybe import of MC3 mutations is responsible, maybe it's some regression. I have an idea how to speed this up anyway. When it comes to sole existence of the /protein/browse page: I think that we may want to remove it, though it could be useful for some users, and keeping it does not cost anything. Please, let me know what you think. *We already precompute if a mutation is PTM related or not (at import), now we would want to precompute sums of such mutations for each protein for possibly all datasets (and maybe site types?). |
Looking at this again - I think "explore all genes" and "explore all proteins" are two redundant views. We should keep one and remove the other, perhaps by viewing main isoform by default and making a checkbox "show all isoforms". Regarding (4) above: let's use radio buttons instead of dropdown menus. Then all options will be visible immediately. There are four each (five with "all" option) so this should not be a major burden. |
Browsing these genes page by page still feels a little arbitrary because it is ultimately an alphabet soup and some numbers (no biologist will know all these genes by heart). Perhaps these two additions may help:
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Point two from above may actually improve our browsing of pathways as well. I will comment separately under the pathways view. |
All right, I will retire the table view for browsing proteins. So let's assume all the points relate to gene browsing:
Done (already in)
Done.
Ye, it is.
Done (filters were already in, recently converted to radio buttons).
An editable box available under "Genes" title, visible after login.
Done
What would be the difference to gene lists we already have? |
The page https://activedriverdb.org/protein/browse/ has a little too much information and should be compressed. I actually wonder if this type of a view is even necessary given that we have top 100 disease genes in a view.
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