Thank you for you suggestions. Would take these into consideration.
Hi,
I am going to do a hybrid assembly for a plant using Illumina and Nanopore reads with the help of the MasuRCA tool. Prior to this I would like to run Genomescope.
My doubt is which reads should I use to run Genomescope ? At first I did an assembly using only short reads and for that I had estimated a genome size using Genomescope. So would that value change now that I am doing hybrid assembly ?
Hope someone would help me.
Thank you.
1 answer
How big is your plant genome and how much coverage do you have ? Also what is your data quality (Q20 etc, or better percent alignment to a close reference genome ?). Or just pore eg 9.4.1 or 10.4.1 and sequencing date ?
I would use Shasta (if 20-60X) or Flye (if 20X +) depending on genome size, if you have enough coverage.Masurca is older,and slower I believe.
Use the Illumina reads for downstream polishing instead.
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