Package to design primers for RACE PCR

Description

You can use this package to design 3' and 5’primers for Race PCR. The design is based on the method described by Clonetech Race PCR manual. The resulting primers will have vector sequence automatically added to them. Source code is available on my Github page.

Installation

library(devtools)

install_github(“lrjoshi/RacepcR”)

Usage

getDNA(dnaseq) #enter DNA Sequence and check length

quality (dnaseq) #to see if your sequence contains character other than AGTC.

gcbarplot(dnaseq) #gives barplot of nucleotide content

get5prime(dnaseq,x) #gives you 5' primer

get3prime(dnaseq,y) #gives you 3' primer

Arguments

dnaseq : it is the sequence of your DNA. For eg : “aaggcctt”

x :position where you want to start your 5' primer

y :position where you want to start your 3' primer

Note

This package depends on Biostrings package. So, you should have already installed Biostrings package from Bioconductor.

Examples

library (RacepcR)

library(Biostrings)

getDNA(“aaggccttcc”)

quality (“aaggcct”)

gcbarplot(“aaaaagccggt”)

get5prime(“aaaggcggcggcttcggcgcgctcgtgctgctgctgcggcgctcctttcgctcgtcgctgctttctctcgct”,30)

get3prime(“aaaggcggccccctcttcggccttcgctgctgctgcggcgcggctcgcgctgctgctttgctgctcgggctcgt”,10)

Lok Raj Joshi
Lok Raj Joshi
Postdoctoral Research Fellow

My research interests include AAV gene therapy, vectored vaccine development, viral pathogenesis, diagnostic assay development,reverse genetics, viral bioinformatics.