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Dear community,
I have 3 huge fastq files for paired end multiplexed read:
I would like to extract from them the common part, so clusters for which I have both reads and multiplexing index. I would like also to have the reads sorted in the same order in all the files.
Do you suggest any software that could help me with it?
I have 3 huge fastq files for paired end multiplexed read:
I would like to extract from them the common part, so clusters for which I have both reads and multiplexing index. I would like also to have the reads sorted in the same order in all the files.
Do you suggest any software that could help me with it?