Open RezwanCAAS opened 8 months ago
I have same issue with --n-hap 3. Only get two haploid genomes.
@tallnuttrbgv I have an idea from the previous publications. Just run the hifiasm with the default settings, e.g., --n-hap 2. Then use your primary assembly and perform the chromosomal scaffolding with Hi-C. RUN EDTA for repeating elements. Then collect a particular major repeating elements covering your all chromosomes. Afterward, perform the alignment among them and clustering will separate the subgenomes.
Unfortunately we will not have HiC for this data. Also HiC will not scaffold if homologous chromosomes have been concatenated as in our case. I need to manually break those contigs.
Sorry for the late reply since I was too busy during the last a few weeks. Right now only the Hi-C module could output more than 2 haplotypes. We would like to apply it to the non-Hi-C module soon as well.
Hi, I am using the allotetraploid plant species to assemble the genome. I have the 3 cells PacBio HiFi reads data to assemble the genome. I ran the code as given following using hifiasm/0.19.8 version
hifiasm -o axm_assembly -t 32 --n-hap 4 axmcell*
this code output is two hap1 and hap2 files, but I was expecting should have 4 hap files as per --n-hap 4 function.
Later i ran default code for hifiasm and this code produced same two hap1 and hap2 as I was expecting to have two hap files. hifiasm -o axm_assembly -t 32 axmcell*
is there something wrong here? or which code should I use for tetraploid? Please mention some suggestions for this. Looking forward.