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I am using wtdbg2 for my plant genome assembly. I have run the wtdbg2 with the same PacBio Sequel CLR long reads and same "-x sq" parameters for a few rounds, but the outputs for each rounds are different where I will get different contig number and also different contig size each time. Is this normal for wtdbg2?
My another question is if I want to run the wtdbg2 with my CANU corrected.fasta file, should I use the "-x corrected" parameters mentioned in the wtdbg2 --help?
Thank you.
Best regards,
Teo
The text was updated successfully, but these errors were encountered:
The differences are expected in multiple-thread and no harm, because wtdbg2 cannot grant to reproduce the same node set in node-selecting, which is somehow with random. --load-XXX will help you to reduce the duplicated process and reproduce the result.
Dear Ruanjue,
Good day!
I am using wtdbg2 for my plant genome assembly. I have run the wtdbg2 with the same PacBio Sequel CLR long reads and same "-x sq" parameters for a few rounds, but the outputs for each rounds are different where I will get different contig number and also different contig size each time. Is this normal for wtdbg2?
My another question is if I want to run the wtdbg2 with my CANU corrected.fasta file, should I use the "-x corrected" parameters mentioned in the wtdbg2 --help?
Thank you.
Best regards,
Teo
The text was updated successfully, but these errors were encountered: