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08-09-2018, 04:46 AM
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Junior Member
Location: Turkey Join Date: Aug 2018
Posts: 1
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What's the exact pathway to handle paired end fastq data so you finally make it into
I've unmapped cleaned paired end sequence data in fastq format of a bacterial genome. I want to get a sequence data in Genbank format in the end. What's the exact pathway that I have to follow in galaxy webserver and if in somepoint necessary, also using linux based apps? I would aprecciate if it would be a detailed exact pathway.
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| annotation, bioinformatics, genome |
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