Comments (4)
Hello,
for the polishing phase, we recommend the following:
- one time using Racon and Nanopore reads
- one time using Medaka and Nanopore reads
- two times using Hapog and Illumina reads
This gave us the best results on most genomes.
from hapo-g.
I will follow your recommendations. Thanks for your help.
Romulo
from hapo-g.
If one had Illumina and Hifi reads, do you have any recommendations on polishing round order and number? Based on your recommendation above, it seems plausible to run Racon with Hifi once then Hapog twice with Illumina. You also mention a 6 round polishing at the end of your manuscript, but I wasn't clear on the order (3 hifi rounds followed by 3 illumina round maybe?). Any help much appreciated. -ian
from hapo-g.
Hello,
if your assembly was made with hicanu or hifiasm, I don't think that a polishing step is required because your assembly will already reach Q45-Q50 with HiFi reads alone. I may be wrong there because we did not investigate the impact of polishing on HiFi assemblies but that is what I observe on our own data.
If you want to try it if you think that it could be beneficial for the quality of your assembly, I think that doing one polishing with hapog and Illumina reads and one polishing with hapog and HiFi reads would probably lead to the most results.
In the manuscript, we tried up to 6 rounds to see if there were any significant changes in quality but the only real gains occured before 2 rounds of polishing. I don't think that this amount of polishing steps (I mean the 6 rounds) will ever be needed to achieve a great genome assembly quality.
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Related Issues (20)
- Conda install fails HOT 3
- Polish before or after Redundans HOT 1
- ModuleNotFoundError HOT 1
- Error with --threads 1 HOT 1
- Minimum coverage for correction? HOT 2
- PackageNotFoundError HOT 4
- How do I get a vcf file? HOT 2
- ERRORs when using newest version on conda HOT 1
- hapog introduce non-codon character in the polished sequence HOT 13
- Question: how HAPO-G handles N in reads? HOT 4
- Question: how about polishing a phased diploid genome assembly? HOT 2
- Memory issue HOT 5
- Explanation of hapog.changes HOT 1
- TypeError issue HOT 12
- long and short reads HOT 1
- Does HAPO-G correct ambiguous bases in fasta
- Error with --threads 1 - persisting HOT 4
- Plant genome HOT 7
- High RAM consumption in plant genome HOT 10
- Phased assembly polishing
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