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fatal error #719
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Hi Paul, --limitOutSJcollapsed requires a positive integer number. The default value is usually fine, please first try without specifying this parameter at all. Cheers |
Hi Alex,
As per your recommendation I used 2.7.2a but again got same error:
EXITING because of fatal error: buffer size for SJ output is too small
Solution: increase input parameter --limitOutSJcollapsed
Aug 24 00:06:49 ...... FATAL ERROR, exiting
I didn’t use —limitOutSJcollapsed flag in my script.
Parul
… On Aug 23, 2019, at 10:59 AM, Alexander Dobin ***@***.***> wrote:
Hi Paul,
--limitOutSJcollapsed requires a positive integer number. The default value is usually fine, please first try without specifying this parameter at all.
Also, I would recommend using more recent stable releases such as 2.6.1d or 2.7.2a .
Cheers
Alex
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Hi Parul, please send me the Log.out file of this failed run. Cheers |
Here you go!
Parul
… On Aug 26, 2019, at 11:06 AM, Alexander Dobin ***@***.***> wrote:
Hi Parul,
please send me the Log.out file of this failed run.
Cheers
Alex
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Hi Parul, it did not get attached. I think you need to do it from the web-site. Cheers |
Hi Alex,
I hope this would work, let me know if not.
Thanks,
Parul
… On Aug 26, 2019, at 11:32 AM, Alexander Dobin ***@***.***> wrote:
Hi Parul,
it did not get attached. I think you need to do it from the web-site.
Cheers
Alex
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No, still no attachment... You can email it to me: dobin @ cshl . edu |
Got it, thanks! Cheers |
Thanks much Alex.
Parul
… On Aug 26, 2019, at 12:52 PM, Alexander Dobin ***@***.***> wrote:
--limitOutSJcollapsed 2000000
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Hi Alex, I couldn't figure out the explanation of this parameter < limitOutSJcollapsed >, may you specify it again? Thanks a lot ! |
Hi Dirac, STAR records the splice junctions detected in the mapped reads, and --limitOutSJcollapsed defines the maximum number of splice junctions. It is used to pre-allocate arrays to store SJ information. Cheers |
I get the same error working with some single nucleus RNAseq data. Is there a parameter somewhere I should change for single nucleus RNAseq data (lots of intronic / immature mRNAs), or perhaps I should edit the gtf file? |
if you get the same error, you need to increase Cheers |
Is tweaking |
Hi Alan, yes, this problem will always generate exit code 104, but other problems may generate this code as well. |
We're trying to make a workflow that auto-scales resources when a job fails. Is the only way to determine what to scale to parse the logs? The current version starts by explictly setting the default: Is there a list of exit codes? Is there a list of things that would scale automatically? Historically, this is the only error we've seen that gets addressed this way, but I haven't reviewed the code to see if there are others. Thank you @alexdobin ! |
Hi Alan, in the beginning, I was trying to keep different exit codes for different classes of errors, but since no one was using them, I stopped doing carefully. |
Hi,
I am using STAR-2.6.0a for custom genome index and paired end reads and getting following error:
EXITING because of fatal error: buffer size for SJ output is too small
Solution: increase input parameter --limitOutSJcollapsed
Aug 23 08:37:22 ...... FATAL ERROR, exiting
options I used:
--genomeLoad NoSharedMemory --genomeDir --runThread 1 --readFilesIn --outSAMtype BAM Unsorted --limitOutSJcollapsed int>0 --outFileNamePrefix
same error with and without using this flag : --limitOutSJcollapsed int>0
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