Hi,
I am trying to use GUAVA and realized that my sequencing files have been split up in several fastq files. Is there a way to align the reads using GUAVA if there are several fastq files for one sample?
At the moment there is no way to feed multiple R1 and R2 fastq files.
But you can concatenate those together using 'cat command'.
Then use it for processing.
Hi, I am trying to use GUAVA and realized that my sequencing files have been split up in several fastq files. Is there a way to align the reads using GUAVA if there are several fastq files for one sample?
Thanks in advance!