Closed mictadlo closed 3 years ago
Hello again,
Firstly, it looks like the matches worked for the most part, and you may not need the -D
option.
The usage of match_part
and match
are standard terms that are hardcoded in the script. Depending on what you wanted, it might be easiest to change them with sed
in your output file.
There is no Name=
tag in the current version. I suppose I could make this, though I'm not sure I understand what you are trying to do here with the names. The subject seq name is including in the Target
tag. If what you are trying to do is display the name/number of each gene and/or its target under the blue box, then you need to configure jbrowse/apollo to display the target for each feature, and not just the parent feature. Unfortunately I don't know how to do that myself.
Also, it looks like you are getting multiple overlapping blocks probably due to multiple isoforms at each locus. For clarity, you may want to either remove those, or pick a single "canonical" protein for each locus (like keep only t1 from augustus), and then run diamond again.
Hope this helps
Hi all, I ran
microsynteny.py -b no_remark.out -q Q.no_remark.mRNA.gff3 -d NbR.no_remark.mRNA.gff3 -D "|" --make-gff > Q-NbR.no_remark.mRNA.microsynteny.gff3
Diamond's BLASTp output:
GFF Query:
GFF Target
The resulting GFF3 file:
Query browser:
Target browser:
match_part
tomatch
in order to create easier to read names e.g.Name=NBlab01G14990.1-vs-NBqld01G09150.1
?-D "|"
correctly?Thank you in advance,
Michal