Hello,
How can I connect in the workflow SamToFastq and Bowtie2 tools in Galaxy? I am trying to convert (filtered) bam to 2 paired end fastq files and map them with bowtie. Apparently, the current version of SamToFastq is missing the fastq outputs in the user interface. It only has report (txt) output. I tested this on a local Galaxy instance and on https://usegalaxy.org. The tool versions are: SamToFastq extract reads and qualities from SAM/BAM dataset and convert to fastq (Galaxy Version 1.136.0) Bowtie2 - map reads against reference genome (Galaxy Version 2.2.6.2)
Note that an older version of the same tool does not have this issue and can be connected with the noodle (tested on local Galaxy instance): SAM to FASTQ creates a FASTQ file (Galaxy Version 1.56.1)
Thank you!
Timur
This looks like a bug. Under review, feedback soon. Thanks for reporting the issue so clearly. Jen, Galaxy team