Closed YiweiNiu closed 6 years ago
Thanks for interesting.
The inside consensus tool wtdbg-cns
aims to provide a quick way to reduce sequencing errors. It is suggested to use Quiver and/or Pilon to polish the consensus sequences after you feel happy with the assembly. Usually, wtdbg-cns
can reduce error rate down to less than 1%, which can be well-aligned by short reads.
BTW, the paper used strage parameters for wtdbg, limited to say wtdbg always ranked last, I had emailed the author just after its publish.
Thank you for your reply!
Good to know the error rate of the wtdbg-cns
results.
BTW, I know wtdbg
and smartdenovo
through this paper. After trying several pipelines (Canu, MECAT, miniasm, MaSuRCA, Flye etc.), wtdbg
is the fastest and the best (at least the most satisfying N50) so far. I will use the results of wtdbg
for downstream analysis.
Thank you for your great tools again!
Have a good luck!
Hi Jue,
I'm sorry to bother you once anain.
I found a evaluation paper and it says (paragraph 11 of "Discussion"):
So I'm wondering that if it is necessary to further run consensus tools after running
wtdbg1.1.006
,wtdbg1.2.8
andsmartdenovo
now, such as Racon? I know all three tools have consensus modules, and have been updated since this paper was published.I'm working on a de novo genome assemlby project and there are very limited genomic resources to evaluate the correctness. Except PacBio data, I also have several short reads libraries, so I want to perform scaffolding based on results of
wtdbg
. I don't know how the errors in contigs affect the scaffolding.Any suggestions or thoughts would be appreciated. Thank you!
Bests, Yiwei Niu