Dear experts,
I have two fastq files contains RNASeq reads of two technical replicates (at the level of re-run the sequencing machine twice) for one sample. I want to select the reads that appear in both fastq files by comparing the sequence reads between two files. How can I do that? does any of the bioinformatics tools do it?
I have two fastq files contains RNASeq reads of two technical replicates (at the level of re-run the sequencing machine twice) for one sample. I want to select the reads that appear in both fastq files by comparing the sequence reads between two files. How can I do that? does any of the bioinformatics tools do it?
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