# An Introduction to sangeranalyseR

Author: Kuan-Hao Chao (u7022787@anu.edu.au)

#### Last update: 19 May, 2021

    library(sangeranalyseR)

# 1 Introduction

sangeranalyseR is an R package for analysing Sanger sequencing reads, especially those from ABIF platform, in pure R environment. There are three levels in sangeranalyseR which are ‘SangerRead’, ‘SangerContig’ and ‘SangerAlignment’. Users can choose which level to start the analysis. In this documentation, we intoduce analysis workflow step by step in these three levels with examples.

# 2 SangerRead

‘SangerRead’ extends from ‘sangerseq’ class and stores ‘abif’ class in sangerseqR as well as essential information including quality trimming and chromatogram parameters. It corresponds to a single ABIF file in Sanger sequencing.

## 2.1 Create SangerRead Instance

First step is to create a ‘SangerRead’ instance. Here, we find the the abosulte file path and assign it to `A_chloroticaFdReadFN`.

    inputFilesPath <- system.file("extdata/", package = "sangeranalyseR")

    A_chloroticaFdReadFN <- file.path(inputFilesPath,
                              "Allolobophora_chlorotica",
                              "RBNII",
                              "Achl_RBNII396-13_1_F.ab1")

Now we can create a ‘SangerRead’ instance by running `SangerRead` constructor function.

    singleRead <- SangerRead(readFeature   = "Forward Read",
                             readFileName  = A_chloroticaFdReadFN)

## 2.2 Visualize Trimmed Read

Second step is to visualize the trimmed read. `qualityBasePlot` triggers a plot_ly interactive plot for users to check the result of the trimmed read.

    qualityBasePlot(singleRead)

## 2.3 Update Trimming Parameters

Third step is to change trimming parameters. `SangerRead` constructor function uses default trimming parameters. If users are not satisfied with the trimming result, they can run `updateQualityParam` function to change the trimming parameters inside the ‘SangerRead’ instance.

    updateQualityParam(singleRead,
                       TrimmingMethod         = "M1",
                       M1TrimmingCutoff       = 0.0003,
                       M2CutoffQualityScore   = NULL,
                       M2SlidingWindowSize    = NULL)

## 2.4 Write FASTA file

Fourth step is to export DNA sequence to FATA file. `writeFastaSR` let users to write read in ‘SangerRead’ instance to file in FASTA format.

    writeFastaSR(singleRead)

    ## [1] "D:\\biocbuild\\bbs-3.13-bioc\\tmpdir\\Rtmpk7Bnay/Achl_RBNII396-13_1_F.fa"

## 2.5 Generate Report

Fifth step is to create a static html report for ‘SangerRead’ instance by running `generateReportSR` function

    generateReportSR(singleRead)

# 3 SangerContig

‘SangerContig’ contains two lists of ‘SangerRead’ which are forward and reverse read list. It also contains alignment results and consensus read. It corresponds to a contig in Sanger sequencing.

## 3.1 Create SangerContig Instance

First step is to prepare all reads in the same directory and define the project parameters.

- `inputFilesParentDir` is the directory storing all raw ABIF files.
- `contigName` is the name of contigs. All targets share the same contig name.
- `suffixForwardRegExp` is the regular expression for forward read suffix.
- `suffixReverseRegExp` is the regular expression for reverse read suffix.

    rawDataDir <- system.file("extdata", package = "sangeranalyseR")
    inputFilesParentDir <- file.path(rawDataDir, "Allolobophora_chlorotica", "ACHLO")
    contigName <- "Achl_ACHLO006-09"
    suffixForwardRegExp <- "_[0-9]*_[F].ab1"
    suffixReverseRegExp <- "_[0-9]*_[R].ab1"

After defining parameters, users can create ‘SangerContig’ instance by running `SangerContig` constructor function.

    sangerContig <- SangerContig(parentDirectory      = inputFilesParentDir,
                                 contigName           = contigName,
                                 suffixForwardRegExp  = suffixForwardRegExp,
                                 suffixReverseRegExp  = suffixReverseRegExp)

## 3.2 Launch Shiny App

Second step is to trigger ‘SangerContig’ Shiny app. In `SangerContig` constructor function, all forward and reverse reads in this contig share the same trimming parameter by default. It is inconvenient for users to check reads one by one through R command; therefore, we provide a local Shiny app to let users easily browse and change parameters in each read in the ‘SangerContig’ instance.

    launchAppSC(sangerContig)

## 3.3 Write FASTA file

Third step is to export DNA sequence to FATA file. After changing trimming parameters in each read, users can run `writeFastaSC` function to write results into text file in FASTA format.

    writeFastaSC(sangerContig)

## 3.4 Generate Report

Fourth step is to create a report. Users can create a static html report for the ‘SangerContig’ instance by running `generateReportSC` function.

    generateReportSC(sangerContig)

# 4 SangerAlignment

‘SangerAlignment’ contains a list of ‘SangerContig’ and the alignment results for all contigs. It corresponds to a rebuild DNA sequence fragment in Sanger sequencing.

## 4.1 Create SangerAlignment Instance

First step is to prepare all reads in the same directory and define the project parameters.

- `inputFilesParentDir` is the directory storing all raw ABIF files.
- `suffixForwardRegExp` is the regular expression for forward read suffix.
- `suffixReverseRegExp` is the regular expression for reverse read suffix.

    rawDir <- system.file("extdata", package="sangeranalyseR")
    parentDir <- file.path(rawDir, "Allolobophora_chlorotica", "RBNII")
    suffixForwardRegExp <- "_[F]_[0-9]*.ab1"
    suffixReverseRegExp <- "_[R]_[0-9]*.ab1"

Users can create ‘SangerAlignment’ instance by running `SangerAlignment` constructor function.

    sangerAlignment <-
            SangerAlignment(parentDirectory = parentDir,
                            suffixForwardRegExp = suffixForwardRegExp,
                            suffixReverseRegExp = suffixReverseRegExp,)

## 4.2 Launch Shiny App

Second step is to run `launchAppSA` to trigger the local ‘SangerAlignment’ Shiny app. Users can easily browse all ‘SangerContig’ instance in ‘SangerAlignment’ and change ‘SangerRead’ trimming parameters in each ‘SangerContig’ instance.

    launchAppSA(sangerAlignment)

## 4.3 Write FASTA file

Third step is to run `writeFastaSC` function to write results into text file in FASTA format.

    writeFastaSA(sangerAlignment)

## 4.4 Generate Report

Fourth step is to create a report. Users can create a static html report for the ‘SangerAlignment’ instance by running `generateReportSA` function.

    generateReportSA(sangerAlignment)