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Span based search #61
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we might want to consider making this independent of the nearest gene service; I could imagine, for example, selecting a macrosynteny block and have that determine the span to be searched. And although |
another note to future selves (mostly future Alan) when it comes to implementing this one; there seems to be no reason in principle why this couldn't be extended to a multispan mode so that we could complete our set of options with pleasing symmetry:
One could imagine a set of spans being determined by something like a query (not the responsibility of GCV) for the set of regions associated with a trait across a number of species (ie QTLs or GWAS-defined areas). Also note that 4) would be a nice way of getting from search mode into multi-alignment mode; although possible now using the families trick it suffers from the problem that any track having a deletion of the selected gene family will be left behind.... |
@sammyjava can you remind me of your use case for this so we can take into account when setting priorities for our next round of development? |
Just the CSw8 example: I've got a genomic range from QTL markers, and I'd like to simply enter the range between the first and last to get the corresponding range on the context viewer. |
FWIW, Nevin Young also asked for this functionality... |
And nearly a year later, Nevin still yearns for it; let's make it happen before Ardmore! |
Commit a4b6c6d updated the Search component to alert the user when a span request is being processed and when it fails. The SpanSearch guard now immediately directs users to the search view and doesn't redirect if the span request fails. Edit: This should be considered a temporary solution until we settle on how to handle fuzzy searches, as discussed in issue #94. |
Added support for spans defined using the ".." syntax in commit 67ed8ae. |
In the search view, the user should be able to provide a genomic interval for a chromosome, perhaps on the current query chromosome, for which to perform a new search. Ideally this would just be a matter of expanding the UI to allow the user to interact with the existing "Nearest Gene" service.
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