Hello everyone, I have in-house sequenced raw transcriptome data. The issue is, that the number of reads for different samples are varying by a huge margin. Eg: one fastq file has approx 10 million reads where as the other file has approx 70 million reads. Is there a way to remove reads from the second file to bring it down to approximately the same size as the previous one without introducing any biases before going ahead with differential expression analysis?
Question: unequal fastq files
9 months ago by
sagardesai91 • 50
IBAB, Bengaluru, India
sagardesai91 • 50 wrote:
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