animal_mt #192
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Hi, I want to use GetOrganelle for assembly of animal mitochondrial genome with Illumina reads. The reads were polished with a pipeline including trimming and merging. The polished reads are composed of merged forward and reverse reads and unpaired read files. I was confused about which data I should continue with for GetOrganelle run and which mode -paired end or single end- I should use for unpaired data. If possible, I would like to hear your suggestions. Thank you so much! |
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Please find a short instruction here. Basically, we do not recommend reads polishing. We also do not have options for merged paired-end reads.
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Please find a short instruction here. Basically, we do not recommend reads polishing. We also do not have options for merged paired-end reads.
-1
and-2
are for paired-end reads, while-u
is for unpaired reads (multiple files split with commas).