puzzle
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Variant caller GUI + genetic disease analysis
This would create a way to narrow the analysis to custom regions
Creating this issue to gather similar issues in one. In general we need suggestions of how to pick these from the vcf, what are the common named keys, are they...
It takes a couple of seconds to load 10K variants in memory, would be nice to give some feedback to the user. Something like for example a modal saying that...
This is a project that we could use but it only works on OSX https://github.com/burrows-labs/pyship
...and allow listing/filtering of only "tagged"/commented variants
I use these all the time when working directly against gemini. http://gemini.readthedocs.org/en/latest/content/querying.html#gt-filter-filtering-on-genotypes For example: ``` gemini query --header \ -q "SELECT chrom,start,end,gene,impact,impact_severity,codon_change,aa_change,aa_length, \ cadd_scaled,clinvar_gene_phenotype,(gts).(*),(gt_ref_depths).(*),(gt_alt_depths).(*) \ FROM variants WHERE (max_aaf_all
Would be nice to have (hardcoded for now): - [ ] HPA - [ ] entrez - [ ] STRING - [ ] Reactome
Here are some suggestions for improving the filtering ui: - [ ] Sliders as input for numeric inputs: frequency filtering, CADD scores and (not implemented) SV size for example -...