| | 1 | == xQTL LL user workshop Fri 28 Oct 2011 general comments == |
| | 2 | * Need more download formats: STATA, SAS, CSV (not TSV) |
| | 3 | * SNP data should somehow include metadata such as: imputed (yes/no), genome build, reliability, dosage, etc. |
| | 4 | * There should be a way to merge (part of a / a filtered) phenotype set with a genotype set, and retrieve the result |
| | 5 | * The application can be slow, need more speed |
| | 6 | * There are too many tabs, GUI is unclear |
| | 7 | * Need an hourglass (or something) to indicate the application is busy (blackout screen with progress bar when busy, GeneNetwork style?) |
| | 8 | * Making selections is too complex |
| | 9 | * Column paging is confusing |
| | 10 | * Filtering works 'half' (Joris please explain) |
| | 11 | * Data viewer should be able to create selections using your own file |
| | 12 | * Ids should be unreckognizable |
| | 13 | * Searchfilter should work on all measurements by default |
| | 14 | * Filters are lost when a user pages, this is annoying |
| | 15 | * Like other waiting times, applying a filter should cause the app to refresh with a 'wait please' status |
| | 16 | * Merging is pheno- and geno sets is a special case of using shopping cart (batches) to save selections for re-use elsewhere, this should be implemented |
