hifiasm
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Unbalanced homeologous exchanges are collapsed
My allotetraploid genome has a few homeologous regions that are derived from the same diploid ancestral species (unbalanced homeologous exchanges). In the final primary assemblies (p_ctg, hap1.p_ctg and hap2.p_ctg), some of these regions are collapsed. How can I improve the completeness of these regions?
Whether this is resolvable highly depends on the length and sequence divergence of these regions. You have to analyze case by case.