Entering edit mode
7.1 years ago
ropolocan
▴
830
Hello,
I have been assembling mitochondrial genomes with SPAdes, and I have been getting good assemblies. However, someone brought to my attention that SPAdes is optimized for bacterial genomes. I have also assembled viral genomes with SPAdes.
Is SPAdes optimized for bacterial genomes? If it is, how so? Is it appropriate to use it for assembling mitochondrial and viral genomes?
Thanks.
I have always used SPAdes for viral genomes and it has produced good assemblies.
You can try
tadpole.sh
from BBMap for small (viral) genomes. Guide here.I will consider it, thanks. Do you think it would be appropriate to use
tadpole.sh
for mitochondrial genomes? The mitogenomes I am working with are ~17Kb.Sure. It should be fast as well. Make sure your input are not contaminated with other data.
Thanks for your answer, @genomax!
Hi! I'm assembling a mitogenome of 569,630 bp. I'm using SPAdes with 60x coverage and k-mers 47,57,67,77. I got 46 contigs. Then I used tadpole with 100x coverage and k=100 and got 222 contigs. I think that my main problem is that I'm not using the correct values for coverage and kmers.
Does anyone has some advice about this? Thanks a lot in advance :)