Comments (2)
--n-hap
is used to determine the coverage of heterozygous nodes or contigs. For your sample, hifiasm thinks the homozygous coverage is 26, and the heterozygous coverages are 26/2 = 13 and 26/4 = 6 using --n-hap 2
and --n-hap 4
, respectively. Hifiasm keeps any node in the assembly graph with coverage above the heterozygous coverage threshold as a real node, instead of sequencing errors. This is why --n-hap 4
leads to a larger graph. Could you please have a try with --hom-cov 55
and --n-hap 2
? Since bv looking at the k-mer plot, there are only two peaks and the homozygous coverage should be 55.
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Dear author,
I tried your suggestions, and here are the results:
hifiasm --n-hap 2 -t 120 -l 0 --hom-cov 55 the generated .p_ctg.gfa file is of size 56G, and the .p_utg.gfa file is of size 66G.
Since mine is a homologous tetraploid, which form should I choose for assembly, p_ctg or p_utg?
p_ctg N50: 100MB
p_utg N50: 1MB
For the above question, could you provide some debugging suggestions? Thank you for your valuable time and assistance. I sincerely look forward to your response!
from hifiasm.
Related Issues (20)
- line 8: 110334 Aborted(core dumped) HOT 1
- Ultra Long intergration failed: no output for UL kmer counting HOT 3
- missing 8Mb sequences in the assembly HOT 5
- Empty haplotype 2 gfa files by ONT integration HOT 1
- Basic Question About HiFi Input HOT 3
- Spend too long times to run hifiasm HOT 4
- Switch error on X and Y chromosome HOT 2
- *.ovlp.bin file HOT 1
- Resolving switching error (?)
- Interchromosomal misjoin HOT 1
- Read error correction does not reduce the number of kmers present once, twice or three times
- Recreate p_ctg from p_utg HOT 3
- In the diploid assembly, hfiiasm identified a value that did not exist in the k-mer plot as the "homozygous read coverage threshold".
- fungi diploid assemble phasing errors
- What is the strategy for Ultra-long ONT integration? HOT 3
- No further progress after generating *bin files HOT 1
- Issues with Hexaploid Assembly
- Numerous spurious contig overlaps in assemblies HOT 1
- output GFA with J lines in scaffolding mode
- Output that maps repeat shrapnels to unitigs and to scaffolded chromsomes
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