Open RaverJay opened 2 years ago
:) good suggestion, actually we have something in this direction in place in covPipe, @MarieLataretu implemented a process that checks for important mutations and alerts when they are masked by N.
For example, S:N501Y and when here an amplicon drop happens the user will get informed somehow. Am I right, @MarieLataretu ?
status? @MarieLataretu @RaverJay @hoelzer
No time, so i guess this remains in the idea stage :<
For example, S:N501Y and when here an amplicon drop happens the user will get informed somehow. Am I right, @MarieLataretu ?
You can specify a VCF file - the process checks if the position is N/low coverage and if the variation is found exactly as in the VCF or with another ALT. The output is a hand full of VCF files which are transformed into a table for the summary report in covpipe.
I cloud plug this also into poreCov, but we still have to think about the output
The topic came up again and we would like to add Nextclade's missing
column to the summary data table.
missing
is the list of detected N nucleotides in alignment coordinates and after all the insertions are stripped.
Also, we would like to have a closer look at the coverage of the spike.
I added a second fastcov
call with positions to try it out and the plots automatically ended up in the HTML report directly below the full genome coverage plots.
Do you think it's a good place for them, or should they better be published in the results?
sounds good. so it will be in the final report then?
Yes, with the current implementation, they only appear in the HTML report, which makes it a bit long:
I like the Spike-focused plots bc/ they are pretty helpful to briefly check for "masked" regions.
Can we just have a "box" that one can extend to look at these plots? So the normal report does not get longer?
+1 for the hide part
I'll see what I can do :)
You are thinking of the collapsibles we already have in the HTML table, right?
Yeah, something like a button below the genome.coverage plots to expand all the spike zoomed plots
[bottom of the site]
Nice, I like! So with that it should be possible to get a quick idea if mutations are really missing/reverted for a certain lineage or just not called bc/ of low coverage in that region
great love it
On Wed, 30 Nov 2022 at 16:37, Martin Hölzer @.***> wrote:
Nice, I like! So with that it should be possible to get a quick idea if mutations are really missing/reverted for a certain lineage or just not called bc/ of low coverage in that region
— Reply to this email directly, view it on GitHub https://github.com/replikation/poreCov/issues/179#issuecomment-1332359218, or unsubscribe https://github.com/notifications/unsubscribe-auth/AIQSLLQHNS3R7DNCM7QCN7LWK5YEJANCNFSM5JT5DHSA . You are receiving this because you were assigned.Message ID: @.***>
Could also include warnings when N stretches are in important regions, e.g. the spike protein
As any mutations/deletions/insertions are just omitted when the corresponding region isn't covered enough, this might give a better overview what to expect.
Not sure on the details - and no idea where to find the time :D