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mahulchak avatar mahulchak commented on August 19, 2024

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zmz1988 avatar zmz1988 commented on August 19, 2024

Hi,
Thanks for replying me. Yes, I found that lowering the cutoff 2M doesn't introduce more duplicated sequence. So it's fine. But I recently realised that those places that can't be merged are mostly heterozygous places. For example, the reference assembly has seq1(haplotype A) + seq2(haplotype A) in one contig, however the query assembly has contig1(haplotype A) and contig2(haplotype B). Though the reference assembly remains the alternative allele of seq2 (could be aligned to contig2(haplotype B) in query assembly) in the whole genome file as a small contig, but the contig1 and contig2 from query assembly will still not be merged together, as it lacks hints where this haplotype B should be placed.

I'm not sure how I can solve this problem without generating a phased assembly (our species is highly inbred). But I do have quite some gaps because of this reason, though the reference genome are pretty gapless but not with high QV. Do you think whether we could employ gfa file in this case?

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mahulchak avatar mahulchak commented on August 19, 2024

I have not really experimented with gfa file in this context. I will have to think about it.

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