sangeranalyseR: Simple and Interactive Processing of Sanger Sequencing Data in R

sangeranalyseR is feature-rich, free, and open-source R package for processing Sanger sequencing data. It allows users to go from loading reads to saving aligned contigs in a fewlines of R code by using sensible defaults for most actions. It also provides complete flexibility for determining how individual reads and contigs are processed, both at the command-line in R and via interactive Shiny applications. sangeranalyseR provides a wide range of options for all steps in Sanger processing pipelines including trimming reads, detecting secondary peaks, viewing chromatograms, detecting indels and stop codons, aligning contigs, estimating phylogenetic trees, and more. Input data can be in either ABIF or FASTA format. sangeranalyseR comes with extensive online documentation and outputs aligned and unaligned reads and contigs in FASTA format, along with detailed interactive HTML reports. sangeranalyseR supports the use of colorblind-friendly palettes for viewing alignments and chromatograms. It is released under anMIT licence and available for all platforms on Bioconductor (https://bioconductor.org/packages/sangeranalyseR, last accessed February 22,2021) and on Github (https://github.com/roblanf/sangeranalyseR, last accessed February 22, 2021).

Automated summary

sangeranalyseR is a feature-rich, free, and open-source R package for processing Sanger sequencing data, providing users with flexibility in handling individual reads and contigs. It offers a wide range of options for all steps in Sanger processing pipelines and supports the use of colorblind-friendly palettes for viewing alignments and chromatograms.