Comments (7)
Could you please run hifiasm with '-l0' and see what the result looks like? Thanks in advance.
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Which tool are you using? Are you sure the tool itself is correct? How did you convert GFA to FASTA?
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Hi chhylp123,
This is my output with -I0 :
Main genome scaffold total: 928
Main genome contig total: 928
Main genome scaffold sequence total: 714.223 MB
Main genome contig sequence total: 714.223 MB 0.000% gap
Main genome scaffold N/L50: 11/23.151 MB
Main genome contig N/L50: 11/23.151 MB
Main genome scaffold N/L90: 45/1.178 MB
Main genome contig N/L90: 45/1.178 MB
Max scaffold length: 52.188 MB
Max contig length: 52.188 MB
Number of scaffolds > 50 KB: 342
% main genome in scaffolds > 50 KB: 97.19%
The genome size is bigger than i am expecting. My genome size is ~400MB. What would be the good way to work with this? Heterozygosity is ~3.5
Thank, happy holidays.
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Which tool are you using? Are you sure the tool itself is correct? How did you convert GFA to FASTA?
Thanks. As Heng said, which tool did you use to covert GFA to FASTA and calculate N50?
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awk '/^S/{print ">"$2;print $3}' PB4.asm.p_ctg.gfa > PB.asm.p_ctg.fa
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Interesting. Is it possible that you can share the bin files with us? If not, could you please try Purge_dups on -l0 assembly?
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Assembly problems aside, I suggest making a Hi-C heatmap against the contig to see if the assembly makes sense, or if it has concatenated several chromosomes together.
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Related Issues (20)
- Possible missing one haplotype in human assemblies HOT 2
- No haploid.gfa files output in trio-binning mode HOT 3
- Hifi + Hi-c + ONT assembly fails
- In Trio-binning, always more on hap1 despite (almost) same sequences for paternal and maternal
- discontinuous assembly with shorter pacbio hifi reads but high coverage HOT 2
- Is x20 of Hifi data enough to construct draft assembly of 6.5Gb genome? HOT 1
- 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 1
- 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
- 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
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