Hi,
I have a question about fragment size estimation during vg mpmap and rpvg using short-read RNA-seq data. Does the fragment size refer to the cDNA size in the library, rather than the size of a single read in a paired-end setup?
In my data, the single reads are 150 bp, and I estimate the fragment size to be around 300–500 bp. However, during vg mpmap, the fragment length was estimated to be approximately 200 bp. I wonder if this discrepancy could be related to the errors I reported in the rpvg GitHub issue.
Would it be better to set the mean and standard deviation of the fragment size during vg mpmap and rpvg?