yes quality trimming
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I know it has been asked earlier but not able to find clear solution. I need to filter paired fastq files and align using bowtie2. Is there any tools that I am missing to filter fastq files and keep only paired-end in two different files. And, remaining single reads in another file?
Thanks
SS
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Here is a great solution from Heng Li: Combining The Paired Reads From Illumina Run