mirkocelii
mirkocelii
Hi @balwierz ! I guess you have already found a way in the meanwhile :D ! I had the same problem and I created two separate TxDb for "+ genes"...
This would be a great tool !
Hello, I'm interested in the filtering too.
@jwinternitz I think the .gfa file is reporting only the reads used to built the assembly. duplicated or completely overlapping reads are not present. I tried to draw a plot...
Me too! I was looking for that, we probably need to align the reads again on the assembly to get the detailed coverage base by base
I agree with you, detailed coverage information could be interesting for the analysis of tandem repeat regions and rDNA
If hap1 and hap2 are both duplicated, it must be a real tetraploid
I also run hifiasm with hifi reads only (no HiC, no ultra-long reads) with the polyploid parameters, but I only got hap1 and hap2, although my sample looks hexaploid/octaploid based...