Hello,
Thanks for a great and useful assembler. We got wonderful results on different plant genomes.
I am assembling the diploid plant genome of using Hifiasm. According to the documentation, Hifiasm purges haplotig duplications by default and generates a primary assembly (p_ctg) together with two phased haplotype assemblies (hap1 and hap2).
I obtained the following assembly statistics:
The default primary assembly is slightly larger than hap.2 and has a slightly lower L90, whereas hap.2 contains substantially fewer contigs and has a similar N50 and completeness.
My goal is to select a reference genome for downstream population genomic analyses using WGS data from different individuals.
In this situation:
- Would you recommend using the default primary assembly or hap.2 as the population genomics reference?
- Is the primary assembly generally a better haploid representation because it is constructed specifically as the primary output after haplotig purging?
Thank you.
Hello,
Thanks for a great and useful assembler. We got wonderful results on different plant genomes.
I am assembling the diploid plant genome of using Hifiasm. According to the documentation, Hifiasm purges haplotig duplications by default and generates a primary assembly (p_ctg) together with two phased haplotype assemblies (hap1 and hap2).
I obtained the following assembly statistics:
The default primary assembly is slightly larger than hap.2 and has a slightly lower L90, whereas hap.2 contains substantially fewer contigs and has a similar N50 and completeness.
My goal is to select a reference genome for downstream population genomic analyses using WGS data from different individuals.
In this situation:
Thank you.