Dear Authors:
Here is my kmer distribution result from the hifiasm v0.15.4 on ccs hifi reads with default paras. There is no peak and I don't know why would this happen.
I use the hifi data run assembly, here is my code of ccs to hifi:
smrtlink/smrtcmds/bin/ccs -j 30 m64252e_210717_222335.subreads.bam hifi.bamsmrtlink/smrtcmds/bin/bam2fasta -o hifi hifi.bam
The genome size is about 670Mb, the coverage of hifi reads is around 33×.
Could you please give some tips about this ?
Hello,
It is better to give Hifiasm as input the Fasta or Fastq fromat. So first convert your data from .bam to .fq using bam2fastq tool and re-run hifiasm using the script in the tutorial.
goodluck
Dear Authors: Here is my kmer distribution result from the hifiasm v0.15.4 on ccs hifi reads with default paras. There is no peak and I don't know why would this happen. I use the hifi data run assembly, here is my code of ccs to hifi:
![3](https://user-images.githubusercontent.com/61385992/134839650-b17a45d1-5297-46c5-b748-b51f4c9a08e9.png)
smrtlink/smrtcmds/bin/ccs -j 30 m64252e_210717_222335.subreads.bam hifi.bam
smrtlink/smrtcmds/bin/bam2fasta -o hifi hifi.bam
The genome size is about 670Mb, the coverage of hifi reads is around 33×. Could you please give some tips about this ?