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Strand issues for several novel genes in GTF (".", not "+" or "-") #107
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Dear @Juhyun-Kim-0203 I suspect that these transcripts may not have any canonical splice sites, and thus their strand cannot be determined. Probably, I should also make an option for filtering out such "unreliable" transcript predictions. Best |
Dear @Juhyun-Kim-0203 Found a silly bug, it happens when lower-case characters appear in the genome (masked regions). Fixed now in master and will be fixed in the next release, which I plan to do ASAP. Thanks for the report! Best |
Dear Andrey
Thank you for your rapid response!
Is it okay with hard masking?
Thank you!
Juhyun
… Dear @Juhyun-Kim-0203 <https://github.com/Juhyun-Kim-0203>
Found a silly bug, it happens when lower-case characters appear in the
genome (masked regions). Fixed now in master and will be fixed in the next
release, which I plan to do ASAP.
Thanks for the report!
Best
Andrey
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Dear @Juhyun-Kim-0203 For hard-masked genomes I presume minimap won't be able to map the reads and thus the transcript won't be discovered at all. However, if splice sites have "NN" characters the strand will be also reported as ".". Best |
Finally released new version 3.4, which fixes this issue. |
Hi,
I encountered an error stating
assert strand == '+' or strand == '-'
while runningsqanti3_qc.py
. Additionally, I noticed several novel genes with a strand designation of "." in the 7th column intranscript_models.gtf
(figure below)These genes are not mono-exonic.
I utilized the most recent version of isoquant (v3.3.1)
I have notice that similar issues in the past, and you addressed them in a previous version.
However, the problem persists.
Could you assist me in identifying the underlying cause of this issue?
Thank you! : )
JH
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