sangerseqR

DOI: 10.18129/B9.bioc.sangerseqR    

Tools for Sanger Sequencing Data in R

Bioconductor version: Release (3.6)

This package contains several tools for analyzing Sanger Sequencing data files in R, including reading .scf and .ab1 files, making basecalls and plotting chromatograms.

Author: Jonathon T. Hill, Bradley Demarest

Maintainer: Jonathon Hill <jhill at byu.edu>

Installation

To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("sangerseqR")

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("sangerseqR")

 

PDF	R Script	sangerseqR
PDF		Reference Manual

Details

biocViews	SNP, Sequencing, Software, Visualization
Version	1.14.0
In Bioconductor since	BioC 2.14 (R-3.1) (4 years)
License	GPL-2
Depends	R (>= 3.0.2), Biostrings
Imports	methods, shiny
LinkingTo
Suggests	BiocStyle, knitr, RUnit, BiocGenerics
SystemRequirements
Enhances
URL
Depends On Me
Imports Me
Suggests Me	CrispRVariants
Build Report

Package Archives

Follow Installation instructions to use this package in your R session.

Source Package	sangerseqR_1.14.0.tar.gz
Windows Binary	sangerseqR_1.14.0.zip
Mac OS X 10.11 (El Capitan)	sangerseqR_1.14.0.tgz
Source Repository	git clone https://git.bioconductor.org/packages/sangerseqR
Package Short Url	http://bioconductor.org/packages/sangerseqR/
Package Downloads Report	Download Stats