I am currently working on simulating low coverage hifi reads to test my pipeline's performance on low coverage samples.
By using:
pbsim3 - simulate WGS 5X coverage 10 passes raw .sam from .fasta
samtools - convert to .bam
pbtk - merge multiple .bam into one
pbccs - conver .bam into (ccs).bam
pbtk - extract hifi from (ccs).bam
However, when I call variant using pbsv on both ccs.bam and hifi.bam; warning of detected ccs input are prompted in both .bam
Is there anything I have done wrongly? (it seemed the size of .ccs and .hifi are the same though)
Hi all,
I am currently working on simulating low coverage hifi reads to test my pipeline's performance on low coverage samples.
However, when I call variant using pbsv on both ccs.bam and hifi.bam; warning of detected ccs input are prompted in both .bam Is there anything I have done wrongly? (it seemed the size of .ccs and .hifi are the same though)
Code used
pbsim --strategy wgs --method errhmm --errhmm ~/miniconda3/pkgs/pbsim3-3.0.4-h4ac6f70_0/data/ERRHMM-SEQUEL.model --depth 5 --genome ~/HG002_BCM/hg002v1.1.fasta --pass-num 10
ccs 5X10P.bam 5X10P.ccs.bam
extracthifi 5X10P.ccs.bam 5X10P.hifi.bam