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Hello Qiime community,
I need to upload some
community 16S sequencing data to the SRA, which requires
demultiplexed FASTQ files for submission. My data came from an Illumina
MiSeq using a paired-end protocol, and raw data
are contained in R1 and R2 FASTQ files. I first joined paired ends,
demultiplexed the joined sequences file using split libraries. I got my seqs.fna, but I could not get my .qual file.To turn my fasta sequences to fastq it's necessary, right?Through the make_fastq.py command... I never submitted any sequence in the SRA. Could someone help me?
Thanks in advanced!!
All the best, Manu
TonyWalters
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Dec 28, 2016, 8:02:34 AM12/28/16
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Hello Manuela,
I would use the option --store_demultiplexed_fastq with split_libraries_fastq.py, rather than generating .qual files and then converting back to fastq format.
Manuela Ramalho
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Dec 28, 2016, 12:03:25 PM12/28/16
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