I did sequencing twice for one isolate. So, I have two data datasets (four fastq files). I am wondering how to do the unicycler assembly using two datasets together. Should I select the data collection option?
Thanks,
Asia
I did sequencing twice for one isolate. So, I have two data datasets (four fastq files). I am wondering how to do the unicycler assembly using two datasets together. Should I select the data collection option?
Thanks,
Asia
Hello,
To assemble all the data together in one result, use the tool Concatenate to merge the replicates. Do this once for the forward reads and once for the reverse reads.
If a collection is used, then a separate assembly will be created for each pair in the collection.
Note: We have had some problems with this tool recently and when I just tested Unicycler with a collection input, the jobs failed. Single paired inputs worked fine this morning but the jobs are queueing a bit longer again now.
Why the queue is taking longer is not clear yet. Updates will be posted to this thread: https://biostar.usegalaxy.org/p/26313/
Why collection inputs fail is also not clear yet, but a ticket tracking the issue can be followed here for updates: https://github.com/galaxyproject/usegalaxy-playbook/issues/82.
Thanks! Jen, Galaxy team