DOI: 10.18129/B9.bioc.sangerseqR    

This is the development version of sangerseqR; for the stable release version, see sangerseqR.

Tools for Sanger Sequencing Data in R

Bioconductor version: Development (3.9)

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>

Citation (from within R, enter citation("sangerseqR")):


To install this package, start R (version "3.6") and enter:

if (!requireNamespace("BiocManager", quietly = TRUE))
BiocManager::install("sangerseqR", version = "3.9")

For older versions of R, please refer to the appropriate Bioconductor release.


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



PDF R Script sangerseqR
PDF   Reference Manual


biocViews SNP, Sequencing, Software, Visualization
Version 1.19.0
In Bioconductor since BioC 2.14 (R-3.1) (5 years)
License GPL-2
Depends R (>= 3.0.2), Biostrings
Imports methods, shiny
Suggests BiocStyle, knitr, RUnit, BiocGenerics
Depends On Me
Imports Me
Suggests Me CrispRVariants
Links To Me
Build Report  

Package Archives

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

Source Package sangerseqR_1.19.0.tar.gz
Windows Binary (32- & 64-bit)
Mac OS X 10.11 (El Capitan) sangerseqR_1.19.0.tgz
Source Repository git clone
Source Repository (Developer Access) git clone
Package Short Url
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