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For several assemblies we found better N50 metrics for bp.p_ctg.gfa than both bp.hap?.p_ctg.gfa.
Why are why losing continuity when separating haplotypes?
Is it pertinent to scaffold bp.hap?.p_ctg.gfa with bp.p_ctg.gfa?
The text was updated successfully, but these errors were encountered:
bp.hap?.p_ctg.gfa dose not join different haplotigs while bp.p_ctg.gfa joins some of them. Therefore bp.p_ctg.gfa usually has higher continuity at the expense of much fragmented a_ctg.gfa. We think fragmented a_ctg.gfa is not such useful so that half of information might be lost. Another difference is that bp.p_ctg.gfa tends to keep sex chromosomes at once. Just curious: how do you scaffold bp.hap?.p_ctg.gfa with bp.p_ctg.gfa?
By the way, version 0.15 has some minor bugs so that it's better to re-output assemblies with v0.15.1 or current github HEAD.
The easiest way is to align bp.hap?.p_ctg.gfa.fa on bp.p_ctg.gfa.fa with dgenies (http://dgenies.toulouse.inra.fr) and export the query organized as the reference.
Hi,
For several assemblies we found better N50 metrics for bp.p_ctg.gfa than both bp.hap?.p_ctg.gfa.
Why are why losing continuity when separating haplotypes?
Is it pertinent to scaffold bp.hap?.p_ctg.gfa with bp.p_ctg.gfa?
The text was updated successfully, but these errors were encountered: