Make Phenolyzer available in simplified view (Nebula) #726
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adityaekawade
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Apr 6, 2021
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I have addressed this issue in a recent commit. How do we deploy it to Nebula? |
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I can coordinate with Nebula to update their version. We'll get them to update when the analytics is updated to not include the urls and when #727 is also fixed. Remember to move issues that are being worked on into the current sprint, so we know what is actually in progress and what is in planning waiting to move across for work. |
tonydisera
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Jun 18, 2021
* dev: (72 commits) Adding allele frequencies (and maybe also numbers of hets) across ethnic sub-populations. #747 Adding an opentargets.org link to the External Links section of the gene information. #746 We can have multiple ensembl gene ids returned, so make another ajax request based on the ensembl gene id to make sure it's name matches our gene symbol. Adding allele frequencies (and maybe also numbers of hets) across ethnic sub-populations. #747 Provide better separation so that it is clear that allele frequencies are coming from gnomAD genomes. Reword info popup on Filter dialog for how filtering on AF works. #747 Use genome build GRCh38 for platinum demo dataset #750 Reword info popup on Filter dialog for how filtering on AF works. #747 Adding allele frequencies (and maybe also numbers of hets) across ethnic sub-populations. #747 Adding allele frequencies (and maybe also numbers of hets) across ethnic sub-populations. #747 Adding an opentargets.org link to the External Links section of the gene information. #746 Adding an opentargets.org link to the External Links section of the gene information. #746 point to updated revel files in vep-cache have clinvar urls source from current backend rather than hard-coded to aws ones actually remove files, not just update gitignore remove .idea files from commit add gnomad back in and fix clinvar extra annotations functionality put gnomad back in for clinvar change back backend direct clinvar track fix - new backend service to pre-filter variants pulled back, rather than front-end filtering - #739 #739 Check if ClinVar pathogenic variants exceeds 1000 variants and prompt user to continue, suggesting that they view counts instead. Make Phenolyzer available in simplified view - Nebula #726 ...
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