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|
|Bioconductor views||SNP Sequencing Visualization|
|Maintainer||Jonathon Hill <email@example.com>|
|Package repository||View on Bioconductor|
Install the latest version of this package by entering the following in R:
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