annotate fastqc_report.Rmd @ 3:1ed094d8871c draft

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author mingchen0919
date Mon, 07 Aug 2017 21:48:49 -0400
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children e629c2288316
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1 ---
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2 title: "Fastqc report: short reads quality evaluation"
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3 author: "Ming Chen"
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4 output: html_document
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5 ---
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6
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7 ```{r setup, include=FALSE}
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8 knitr::opts_chunk$set(echo=ECHO, warning=FALSE, message=FALSE)
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9 library(plyr)
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10 library(stringr)
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11 library(dplyr)
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12 library(highcharter)
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13 library(DT)
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14 library(reshape2)
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15 # library(Kmisc)
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16 library(plotly)
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17 library(formattable)
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18 library(htmltools)
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19 ```
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20
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21
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22 ```{bash 'create output directory', echo=FALSE}
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23 # create extra files directory. very important!
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24 mkdir REPORT_OUTPUT_DIR
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25 ```
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26
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27 # Fastqc analysis
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28 ```{bash 'copy data to working directory', echo=FALSE}
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29 # Copy uploaded data to the working directory
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30 for f in $(echo READS | sed "s/,/ /g")
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31 do
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32 cp $f ./
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33 done
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34 ```
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35
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36
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37 ```{bash 'run fastqc', echo=FALSE}
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38 for r in $(ls *.dat)
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39 do
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40 fastqc -o REPORT_OUTPUT_DIR $r > /dev/null 2>&1
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41 done
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42 ```
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43
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44 ## Fastqc html reports
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45
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46 Below are links to ***Fastqc*** original html reports.
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47 ```{r 'html report links'}
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48 html_report_list = list()
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49 html_files = list.files('REPORT_OUTPUT_DIR', pattern = '.*html')
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50 for (i in html_files) {
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51 html_report_list[[i]] = tags$li(tags$a(href=i, i))
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52 }
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53 tags$ul(html_report_list)
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54 ```
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55
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56
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57 ## Parsing fastqc data
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58
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59 ```{bash echo=FALSE}
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60 ##==== copy fastqc generated zip files from report output directory to job work directory ==
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61 cp -r REPORT_OUTPUT_DIR/*zip ./
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62
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63 # create a file to store data file paths
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64 echo "sample_id,file_path" > PWF_file_paths.txt # Pass, Warning, Fail
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65 echo "sample_id,file_path" > PBQS_file_paths.txt # Per Base Quality Score
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66 echo "sample_id,file_path" > PSQS_file_paths.txt # Per Sequence Quality Score
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67 echo "sample_id,file_path" > PSGC_file_paths.txt # Per Sequence GC Content
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68 echo "sample_id,file_path" > PBSC_file_paths.txt # Per Base Sequence Content
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69 echo "sample_id,file_path" > PBNC_file_paths.txt # Per Base N Content
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70 echo "sample_id,file_path" > SDL_file_paths.txt # Sequence Duplication Level
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71 echo "sample_id,file_path" > SLD_file_paths.txt # Sequence Length Distribution
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72 echo "sample_id,file_path" > KMC_file_paths.txt # Kmer Content
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73
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74 for i in $(ls *.zip)
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75 do
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76 BASE=$(echo $i | sed 's/\(.*\)\.zip/\1/g')
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77 echo $BASE
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78 unzip ${BASE}.zip > /dev/null 2>&1
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79
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80 ##====== pass,warning,fail (WSF) =============
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81 awk '/^>>/ {print}' "$BASE"/fastqc_data.txt | grep -v 'END_MODULE' | sed 's/>>//' > "$BASE"-PWF.txt
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82 echo "${BASE},${BASE}-PWF.txt" >> PWF_file_paths.txt
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83
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84 ##====== per base quality scores (PBQS) ======
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85 awk '/^>>Per base sequence quality/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-PBQS.txt
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86 echo "${BASE},${BASE}-PBQS.txt" >> PBQS_file_paths.txt
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87
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88 ##====== per sequence quality scores (PSQS)
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89 awk '/^>>Per sequence quality scores/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-PSQS.txt
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90 echo "${BASE},${BASE}-PSQS.txt" >> PSQS_file_paths.txt
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91
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92 ##====== Per sequence GC content (PSGC)
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93 awk '/^>>Per sequence GC content/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-PSGC.txt
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94 echo "${BASE},${BASE}-PSGC.txt" >> PSGC_file_paths.txt
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95
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96 ##====== Per Base Sequence Content (PBSC)
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97 awk '/^>>Per base sequence content/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-PBSC.txt
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98 echo "${BASE},${BASE}-PBSC.txt" >> PBSC_file_paths.txt
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99
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100 ##====== Per Base N Content (PBNC)
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101 awk '/^>>Per base N content/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-PBNC.txt
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102 echo "${BASE},${BASE}-PBNC.txt" >> PBNC_file_paths.txt
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103
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104 ##====== Sequence Duplication Level (SDL)
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105 awk '/^>>Sequence Duplication Levels/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-SDL.txt
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106 echo "${BASE},${BASE}-SDL.txt" >> SDL_file_paths.txt
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107
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108 ##====== Sequence Length Distribution (SLD)
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109 awk '/^>>Sequence Length Distribution/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-SLD.txt
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110 echo "${BASE},${BASE}-SLD.txt" >> SLD_file_paths.txt
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111
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112 ##====== Kmer Content ============
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113 awk '/^>>Kmer Content/ {flag=1; next} /END_MODULE/ {flag=0} flag' "$BASE"/fastqc_data.txt >"$BASE"-KMC.txt
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114 echo "${BASE},${BASE}-KMC.txt" >> KMC_file_paths.txt
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115
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116 done
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117 ```
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118
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119
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120 ## Evaluation Overview
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121
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122 ```{r 'overview'}
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123 PWF_file_paths = read.csv('PWF_file_paths.txt',
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124 header = TRUE, stringsAsFactors = FALSE)
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125 rm('PWF_df')
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126 for(i in 1:nrow(PWF_file_paths)) {
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127 file_path = PWF_file_paths[i,2]
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128 pwf_df = read.csv(file_path,
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129 sep='\t', header=FALSE, stringsAsFactors = FALSE)
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130 colnames(pwf_df) = c('item', PWF_file_paths[i,1])
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131 if (!exists('PWF_df')) {
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132 PWF_df = pwf_df
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133 } else {
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134 PWF_df = cbind(PWF_df, pwf_df[,2,drop=FALSE])
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135 }
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136 }
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137 ```
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138
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139 ```{r}
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140 my_icon = c('ok', 'remove', 'star')
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141 names(my_icon) = c('pass', 'fail', 'warn')
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142 evaluate_list = list()
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143 for (i in colnames(PWF_df)[-1]) {
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144 evaluate_list[[i]] = formatter(
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145 "span",
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146 style = x ~ style("background-color" = ifelse(x =='pass', '#9CD027', ifelse(x == 'fail', '#CC0000', '#FF4E00')),
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147 "color" = "white",
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148 "width" = "50px",
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149 "float" = "left",
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150 "padding-right" = "5px")
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151 )
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152 }
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153
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154 formattable(PWF_df, evaluate_list)
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155 ```
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156
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157
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158 ## Per Base Quality Scores
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159
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160 ```{r}
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161 PBQS_df = data.frame()
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162 PBQS_file_paths = read.csv('PBQS_file_paths.txt',
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163 header = TRUE, stringsAsFactors = FALSE)
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164 for(i in 1:nrow(PBQS_file_paths)) {
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165 # file_path = paste0('REPORT_OUTPUT_DIR/', PBQS_file_paths[i,2])
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166 file_path = PBQS_file_paths[i,2]
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167 pbqs_df = read.csv(file_path,
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168 sep='\t', header=TRUE, stringsAsFactors = FALSE) %>%
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169 mutate(Base1=as.numeric(str_split_fixed(X.Base, '-', 2)[,1]),
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170 Base2=as.numeric(str_split_fixed(X.Base, '-', 2)[,2])) %>%
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171 (function (df) {
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172 df1 = select(df, -Base2)
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173 df2 = select(df, -Base1) %>% filter(Base2 != '')
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174 colnames(df1) = c(colnames(df1)[1:7], 'Base')
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175 colnames(df2) = c(colnames(df2)[1:7], 'Base')
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176 res = rbind(df1, df2) %>% arrange(Base)
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177 return(res)
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178 })
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179 pbqs_df$sample_id = rep(PBQS_file_paths[i,1], nrow(pbqs_df))
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180 PBQS_df = rbind(PBQS_df, pbqs_df)
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181 }
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182 ```
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183
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184
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185 ```{r}
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186 # datatable(PBQS_df)
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187 max_phred = max(PBQS_df$Mean) + 10
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188 hchart(PBQS_df, "line", hcaes(x = Base, y = Mean, group = sample_id)) %>%
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189 hc_title(
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190 text = "Per Base Quality Score"
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191 ) %>%
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192 hc_yAxis(
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193 title = list(text = "Mean Base Quality Score"),
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194 min = 0,
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195 max = max_phred,
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196 plotLines = list(
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197 list(label = list(text = "Phred Score = 27"),
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198 width = 2,
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199 dashStyle = "dash",
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parents:
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200 color = "green",
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parents:
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201 value = 27),
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202 list(label = list(text = "Phred Score = 20"),
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203 width = 2,
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parents:
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204 color = "red",
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parents:
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205 value = 20)
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206 )
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207 ) %>%
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208 hc_exporting(enabled = TRUE)
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209 ```
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parents:
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210
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211
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212 ## Per Base N Content
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213
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214 ```{r}
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215 PBNC_df = data.frame()
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216 PBNC_file_paths = read.csv('PBNC_file_paths.txt',
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217 header = TRUE, stringsAsFactors = FALSE)
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218 for(i in 1:nrow(PBNC_file_paths)) {
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219 # file_path = paste0('REPORT_OUTPUT_DIR/', PBNC_file_paths[i,2])
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220 file_path = PBNC_file_paths[i,2]
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221 pbnc_df = read.csv(file_path,
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222 sep='\t', header=TRUE, stringsAsFactors = FALSE) %>%
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223 mutate(Base1=as.numeric(str_split_fixed(X.Base, '-', 2)[,1]),
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224 Base2=as.numeric(str_split_fixed(X.Base, '-', 2)[,2])) %>%
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225 (function (df) {
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226 df1 = select(df, -Base2)
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227 df2 = select(df, -Base1) %>% filter(Base2 != '')
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228 colnames(df1) = c(colnames(df1)[1:2], 'Base')
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229 colnames(df2) = c(colnames(df2)[1:2], 'Base')
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230 res = rbind(df1, df2) %>% arrange(Base)
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231 return(res)
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232 })
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233 pbnc_df$sample_id = rep(PBNC_file_paths[i,1], nrow(pbnc_df))
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234 PBNC_df = rbind(PBNC_df, pbnc_df)
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235 }
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236 ```
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237
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238
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239 ```{r}
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240 PBNC_df$N.Count = PBNC_df$N.Count * 100
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241 max_phred = max(PBNC_df$N.Count) + 5
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242 hchart(PBNC_df, "line", hcaes(x = as.character(Base), y = N.Count, group = sample_id)) %>%
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243 hc_title(
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244 text = "Per Base N Content"
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245 ) %>%
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246 hc_xAxis(
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247 title = list(text = "Base Position")
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248 ) %>%
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249 hc_yAxis(
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250 title = list(text = "N %"),
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251 plotLines = list(
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252 list(label = list(text = "N = 5%"),
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253 width = 2,
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254 dashStyle = "dash",
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parents:
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255 color = "red",
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256 value = 5)
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257 )
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258 ) %>%
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259 hc_exporting(enabled = TRUE)
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260 ```
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parents:
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261
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parents:
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262
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263
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264
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265 ## Per Sequence Quality Scores
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266
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267 ```{r}
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268 PSQS_df = data.frame()
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269 PSQS_file_paths = read.csv('PSQS_file_paths.txt',
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270 header = TRUE, stringsAsFactors = FALSE)
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271 for(i in 1:nrow(PSQS_file_paths)) {
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272 # file_path = paste0('REPORT_OUTPUT_DIR/', PSQS_file_paths[i,2])
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273 file_path = PSQS_file_paths[i,2]
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274 psqs_df = read.csv(file_path,
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275 sep='\t', header=TRUE, stringsAsFactors = FALSE)
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276 psqs_df$sample_id = rep(PSQS_file_paths[i,1], nrow(psqs_df))
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277 PSQS_df = rbind(PSQS_df, psqs_df)
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278 }
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279 ```
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280
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281
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282 ```{r}
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283 max_phred = max(PSQS_df$X.Quality) + 5
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284 hchart(PSQS_df, "line", hcaes(x = X.Quality, y = Count, group = sample_id)) %>%
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285 hc_title(
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286 text = "Per Sequence Quality Score"
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287 ) %>%
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288 hc_xAxis(
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289 title = list(text = "Mean Sequence Quality Score"),
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parents:
diff changeset
290 min = 0,
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291 max = max_phred,
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292 plotLines = list(
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diff changeset
293 list(label = list(text = "Phred Score = 27"),
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parents:
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294 width = 2,
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parents:
diff changeset
295 dashStyle = "dash",
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parents:
diff changeset
296 color = "green",
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parents:
diff changeset
297 value = 27),
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parents:
diff changeset
298 list(label = list(text = "Phred Score = 20"),
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parents:
diff changeset
299 width = 2,
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parents:
diff changeset
300 color = "red",
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parents:
diff changeset
301 value = 20)
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parents:
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302 )
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parents:
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303 ) %>%
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304 hc_exporting(enabled = TRUE)
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305 ```
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parents:
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306
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307
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308 ## Per Sequence GC Content
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parents:
diff changeset
309
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parents:
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310
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311 ```{r}
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312 PSGC_df = data.frame()
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313 PSGC_file_paths = read.csv('PSGC_file_paths.txt',
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314 header = TRUE, stringsAsFactors = FALSE)
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315 for(i in 1:nrow(PSGC_file_paths)) {
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316 # file_path = paste0('REPORT_OUTPUT_DIR/', PSGC_file_paths[i,2])
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317 file_path = PSGC_file_paths[i,2]
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318 psgc_df = read.csv(file_path,
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parents:
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319 sep='\t', header=TRUE, stringsAsFactors = FALSE)
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320 psgc_df$sample_id = rep(PSGC_file_paths[i,1], nrow(psgc_df))
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321 PSGC_df = rbind(PSGC_df, psgc_df)
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322 }
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323 ```
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parents:
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324
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parents:
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325
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326 ```{r}
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327 max_phred = max(PSGC_df$Count) + 5
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328 hchart(PSGC_df, "line", hcaes(x = X.GC.Content, y = Count, group = sample_id)) %>%
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329 hc_title(
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330 text = "Per Sequence GC Content"
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331 ) %>%
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332 hc_xAxis(
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333 title = list(text = "% GC")
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334 ) %>%
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335 hc_exporting(enabled = TRUE)
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336 ```
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parents:
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337
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338
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339 ## Per Base Sequence Content
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parents:
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340
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341 ```{r}
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342 PBSC_df = data.frame()
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parents:
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343 PBSC_file_paths = read.csv('PBSC_file_paths.txt',
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344 header = TRUE, stringsAsFactors = FALSE)
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345 for(i in 1:nrow(PBSC_file_paths)) {
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346 # file_path = paste0('REPORT_OUTPUT_DIR/', PBSC_file_paths[i,2])
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347 file_path = PBSC_file_paths[i,2]
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348 pbsc_df = read.csv(file_path,
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349 sep='\t', header=TRUE, stringsAsFactors = FALSE) %>%
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350 mutate(Base1=as.numeric(str_split_fixed(X.Base, '-', 2)[,1]),
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351 Base2=as.numeric(str_split_fixed(X.Base, '-', 2)[,2])) %>%
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352 (function (df) {
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353 df1 = select(df, -Base2)
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354 df2 = select(df, -Base1) %>% filter(Base2 != '')
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355 colnames(df1) = c(colnames(df1)[1:5], 'Base')
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356 colnames(df2) = c(colnames(df2)[1:5], 'Base')
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357 res = rbind(df1, df2) %>% arrange(Base)
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358 return(res)
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359 })
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360 pbsc_df$sample_id = rep(PBSC_file_paths[i,1], nrow(pbsc_df))
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361 PBSC_df = rbind(PBSC_df, pbsc_df)
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362 }
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363 ```
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364
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parents:
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365
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366 ```{r out.width="100%"}
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367 PBSC_df_2 = select(PBSC_df, -X.Base) %>%
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368 melt(id = c('Base', 'sample_id'), value.name = 'base_percentage')
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369 p = ggplot(data = PBSC_df_2, aes(x = Base, y = base_percentage, group = variable, color = variable)) +
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370 geom_line() +
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parents:
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371 facet_wrap(~ sample_id)
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parents:
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372 ggplotly(p)
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373 ```
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parents:
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374
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parents:
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375
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376 ## References
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parents:
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377
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parents:
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378 * Andrews, Simon. "FastQC: a quality control tool for high throughput sequence data." (2010): 175-176.
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379 * Goecks, Jeremy, Anton Nekrutenko, and James Taylor. "Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences." Genome biology 11.8 (2010): R86.
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380 * Afgan, Enis, et al. "The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update." Nucleic acids research (2016): gkw343.
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381 * Highcharts. https://www.highcharts.com/. (access by May 26, 2017).
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parents:
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382 * R Core Team (2017). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/.
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parents:
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383 * Joshua Kunst (2017). highcharter: A Wrapper for the 'Highcharts' Library. R package version 0.5.0. https://CRAN.R-project.org/package=highcharter
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parents:
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384 * Carson Sievert, Chris Parmer, Toby Hocking, Scott Chamberlain, Karthik Ram, Marianne Corvellec and Pedro Despouy (2017). plotly: Create Interactive Web Graphics via 'plotly.js'. R package version 4.6.0. https://CRAN.R-project.org/package=plotly