Open SquRunner opened 2 weeks ago
You can run the command convert xxx.svg xxx.png yourself convert xxx.svg xxx.png
Thank you for the reply! Sadly this did not working either. I still end up with a blank file. The file size increases a bit? Originally it was 7.3K but now it is 13K.
I have sence tried running a number of other regions as well, none of which are plotting.
Some throw an error:
Can't Found the Site file : chr25_out_LD.site.gz Too many SNP site 4813 , I suggest that you add the Para [-OutPng] to see the png File In Big SNP Number :4813 ,Para -NumGradien suggest be maxValue : 10 ,auto be it ALL done
And again, the command I used that resulted in this error was: LDBlockShow -InVCF dp8_concat.recode.vcf -OutPut chr25_whole_out_LD -Region chr25:1-700000 -OutPng -NoShowLDist 108720060 -SeleVar 2
svg is only 17k, which is not too big. There may be something wrong with the convert command in your linux system. I suggest you download svg to your local computer, open it with a browser, and then use other screenshot software to convert it to png format.
The svg file is actually 308M. I have tried bringing it locally, but does not like to open in the browser. The convert function seems to work for some regions, but not most.
You can retry running this command manually on a computer node with large memory.convert xxx.svg xxx.png
I am attempting to plot regions along a genome. I know I have dense SNP data, but some regions work, and others don't? An example of the command for a region that does not work is:
Output File:
Error File:
Thank you for the help!