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Is it possible to merge only Read2 FASTQ? #1

@zymeth123

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@zymeth123

Dear github usearch members.

I apologize asking some helps on this thread, this is my first time I posted at github and I am beginner with NGS especially usearch. To the main point, I have mistakenly produced paired-ends FASTQ data with 151 cycles of r1 or r2. But, my target is around 500 bp. Due to no overlapping, is it possible to convert my FASTQ data without merging in usearch? perhaps, could we use only read2 FASTQ for conversion to merging or pipeline?

Thank to the administrator for permitting my post

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