Can I merge two fastq into one in galaxy?

I got chipseq paired-end sequencing data, and I want to merge two fastq into one.
NOT join paired-end into single end.
① T1_L1…R1.fastq.gz
② T1_L2…R1.fastq.gz
Its from two seperate sequencing
I want to merge these two fastq into one.Can I do it in galaxy?If can ,what programe can achieve that? many thanks!

Hello @hpc

The tool Concatenate will “stack” files on top of each other.

Tutorial → Data Manipulation Olympics