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Type: Bug
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Status: Closed
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Priority: Blocker
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Resolution: Won't Fix
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Affects Version/s: 1.26
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Fix Version/s: None
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Component/s: Workflow
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Labels:None
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Affect Type:Userdefined
As a workaround from this https://local.ugene.unipro.ru/tracker/browse/UGENE-3257 , I am now using FASTQ files provided by my sequencing service to analyze Sanger sequencing results.
For one reference sequence, I have a FASTQ file containing all the Sanger reads + the associated quality values.
When I add the file to the input of the "Trim and Align Sanger Reads" workflow, it doesn't work.
But if I manually split the file to many FASTQ files (each one containing only one sequence + its quality values) and add all of them to the input of the workflow, it does work.
It's a bit painful to have to process the FASTQ file before running the workflow.
Do you know how I could fix that ?