Problem for separating reverse and forward reading in my RNA-seq
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5.8 years ago
modarzi ▴ 170

Hi,

For downloading SRA files for my study I used browser. So, for Paired End read in my samples, I downloaded just one .fastq file(example link for download).Now, I have to separate reverse and forward read and my each file should distribute to 2 .fastq file.

I appreciate if any body share his/her R code or Linux code for this problem.

Best regards,

Mohammad

RNA-Seq sequencing Paired End • 1.0k views
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