This tool joins paired end FASTQ reads from two separate files, one with the left mates and one with the right mates, into a single files where left mates alternate with their right mates. The join is performed using sequence identifiers, allowing the two files to contain differing ordering. If a sequence identifier does not appear in both files, it is included in a separate file. |
hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/fastq_paired_end_interlacer
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
on paired end reads | 1.1.5+galaxy2 | 23.1 |