Hi all,
I am a bit unsure about how to structure my input Illumina fastq files. I have:
Paired end Illumina fastq file + 'single end' Illumina fastq file
However, the single end file actually consists of 'left-over' reads from the original paired end files (could have either /1 or /2 tags), where one of the mates has been removed as a result of pre-processing
Specifically:
Can I input paired-end data where some of the pairs are missing their mates? How will those single reads be treated?
Is there any other way I should input both paired end and single end reads together?
Thanks,
Matt