Hi everyone! I am trying to design Prime Editing gRNA. As described on the software package (CRISPRseek, Version 1.27.6) page 22, I've written the following:
inputFilePath<- ("/path/to/the/file.fasta")
pegRNA <- findgRNAs(inputFilePath,
pairOutputFile = "testpairedgRNAs1.xls",
PAM.size = 3L,
gRNA.size = 20L,
overlap.gRNA.positions = c(17L,18L),
PBS.length = 15,
corrected.seq = "C",
RT.template.pattern = "D$",
RT.template.length = 8:30,
targeted.seq.length.change = 0,
bp.after.target.end = 15,
target.start = 506,
target.end = 506,
paired.orientation = "PAMin", min.gap = 20, max.gap = 90,
primeEditing = TRUE,
findPairedgRNAOnly = TRUE,
)
But I get the following error message:
Error in findgRNAs(inputFilePath, pairOutputFile = "testpairedgRNAs1.xls", :
unused arguments (PBS.length = 15, corrected.seq = "C", RT.template.pattern = "D$", RT.template.length = 8:30, targeted.seq.length.change = 0, bp.after.target.end = 15, target.start = 506, target.end = 506, primeEditing = TRUE)
Does anyone have any idea of what I can do to fix this problem? Am I missing something? I want also to mention that "findgRNAs" function works pretty well in finding the regular gRNAs from the same input file.
Here is my session info:
> sessionInfo()
R version 3.6.3 (2020-02-29)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS High Sierra 10.13.6
I'd appreciate it!
Hi Julie,
As suggested, I installed R 4.0 and the right CRISPRseek package. The problem is solved and I could design the pegRNAs as I wanted. I greatly appreciate your help.
Best regards, Giti