Closed carolhsb closed 3 years ago
Hi Carol, which Racon version are you using? How big is the assembly? The command you used seems fine to me at first glance.
Best regards, Robert
Hi Robert,
Thank you for your answer!
I'm using version 1.4.21. The assembly has 1.37 GB.
Cheers,
Carol
Please run the below command from the racon root folder and check if anything is created:
build/vendor/rampler/bin/rampler split dbg.corrected.pb.fasta 28048207
Scratch that, I found the bug.
Hi Robert,
I've tried and it works...it splits the contigs
You can pull the new commit and recompile. It should work now.
You can pull the new commit and recompile. It should work now.
Ok. I will do it.
Thank you so much!!
Don't forget to run git submodule --update --recursive
.
It's working now! :) thank you
Hi,
I'm running racon_wrapper to polish an assembly (that I had previously corrected with PacBio reads) with Illumina reads.
This is the command I'm using:
python3 /home/carol/racon/build/bin/racon_wrapper -t 30 --split 28048207 /home/carol/short_reads_mma/concat.clean.fq.gz ./dbg.illumina.sam ./dbg.corrected.pb.fasta > dbg.corrected.illumina.fasta
I keep getting this error: [RaconWrapper::run] total number of splits: 0 [RaconWrapper::run] error: unable to find split target sequences!
In the split flag, I used the largest contig value.
How can I work it out?
Thanks in advance,
Carol