Hi,
we've been playing around with successive rounds of gapfilling and scaffolding and we see a constant improvement of our genome stats. Basically we run several iterations of gapfilling which generates new ends with potential mapping sites for our mate-pair libraries and re-scaffold the genome. However, besides not being able to really assess the quality of these so generated new scaffolds, we wondered if re-scaffolding after gapfilling should be performed on contig level i.e. gapfilling, breaking down the scaffolds to contigs (now longer thanks to the gapfilling) and rescaffolding, or if it would be rather advisable to re-scaffold the gapfilled scaffolds. Theoretically, breaking down the scaffolds to contigs after gapfilling would allow to intercalate contigs that could not be mapped to the previously existing gaps due to the missing sequence at the end of the contigs before gap filling.
Has anyone played around with this and can share his experience?
Thanks,
Zapp
we've been playing around with successive rounds of gapfilling and scaffolding and we see a constant improvement of our genome stats. Basically we run several iterations of gapfilling which generates new ends with potential mapping sites for our mate-pair libraries and re-scaffold the genome. However, besides not being able to really assess the quality of these so generated new scaffolds, we wondered if re-scaffolding after gapfilling should be performed on contig level i.e. gapfilling, breaking down the scaffolds to contigs (now longer thanks to the gapfilling) and rescaffolding, or if it would be rather advisable to re-scaffold the gapfilled scaffolds. Theoretically, breaking down the scaffolds to contigs after gapfilling would allow to intercalate contigs that could not be mapped to the previously existing gaps due to the missing sequence at the end of the contigs before gap filling.
Has anyone played around with this and can share his experience?
Thanks,
Zapp
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