---
title: "Quality Check Report"
subtitle: "<h4>GWASinspector package</h4>"
output:
  html_document:
    css: styles_extra.css
---






```{r, echo=FALSE}
htmltools::img(src = knitr::image_uri(system.file("extdata", "DNA.png", package = "GWASinspector")), 
               alt = 'logo', 
               style = 'position:absolute; top:0; right:20%; padding:10px;')
```

***

<br/>
QC start time:		**`r format(.QC$thisStudy$starttime, "%b %d %Y - %X")`**

QC end time:		**`r format( .QC$thisStudy$endtime, "%b %d %Y - %X")`**

Script version: **`r .QC$script.version`**

System information : **`r .QC$r.version`**

<br/>


<h3 class="header1">User preferences</h3>
Alterative header file:		**`r basename(.QC$config$supplementaryFiles$header_translations)`**

Allele frequency standard reference dataset:		**`r basename(.QC$config$supplementaryFiles$allele_ref_std)`**

`r if(!is.na(.QC$config$supplementaryFiles$allele_ref_alt)){ 
			paste(sprintf("Allele frequency alternative reference dataset:\t**%s**" , 
			basename(.QC$config$supplementaryFiles$allele_ref_alt)))
			}

`

`r if(!is.na(.QC$config$supplementaryFiles$beta_ref_std)){ 
			paste(sprintf("Effect-size reference dataset:\t**%s**" , 
			basename(.QC$config$supplementaryFiles$beta_ref_std)))
			}

`





<h4 class="header2">Filter values for selecting High-Quality (HQ) variants</h4>

`r 

  filter.table <- data.table(
    "<span class='mainItem'>Allele frequency</span>" =  format(.QC$config$filters$HQfilter_FRQ,
                                 scientific = FALSE))

  ifelse("HWE_PVAL" %in% .QC$thisStudy$renamed.File.Columns.sorted,
    filter.table <- cbind(filter.table, "<span class='mainItem'>HWE p-value</span>" = format(.QC$config$filters$HQfilter_HWE,
                          scientific = FALSE)),
    filter.table <- cbind(filter.table, "<span class='mainItem'>HWE p-value</span>" = "Not included"))

  ifelse("CALLRATE" %in% .QC$thisStudy$renamed.File.Columns.sorted,
    filter.table <- cbind(filter.table, "<span class='mainItem'>Call-rate</span>" =  format(.QC$config$filters$HQfilter_cal,
                          scientific = FALSE)),
    filter.table <- cbind(filter.table, "<span class='mainItem'>Call-rate</span>" = "Not included"))


  ifelse("IMP_QUALITY" %in% .QC$thisStudy$renamed.File.Columns.sorted,
    filter.table <- cbind(filter.table, "<span class='mainItem'>Imputation quality</span>" = format(.QC$config$filters$HQfilter_imp,
                                  scientific = FALSE)),
    filter.table <- cbind(filter.table, "<span class='mainItem'>Imputation quality</span>" = "Not included"))

                                  
  filter.table <- t(filter.table)

  colnames(filter.table) <- 'Value'
  kable(filter.table,escape='FALSE', align = "c",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em") %>%
		kableExtra::column_spec(2, width="10em")
`







<h3 class="header1">Input File Description</h3>


Input file:		**`r basename(.QC$thisStudy$file.path)`**

Input file line count (including header):		**`r .QC$thisStudy$file.line.count`**

Input file ends with a new line:		**`r .QC$thisStudy$file.endsWithNewLine`**



<br/>

<h4 class="header2">Column names</h4>

`r column.tbl <- rbind(.QC$thisStudy$original.File.Columns.sorted,
.QC$thisStudy$renamed.File.Columns.sorted)
rownames(column.tbl) <- c('Original', 'Renamed')

kable(column.tbl, align = "c" , format = "html") %>% 
kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
full_width = F, 
position = "left") %>%
kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
kableExtra::column_spec(2, width = "10em") %>%
kableExtra::scroll_box(width = "100%")
`
<div class="footnote1">
*Header values are translated according to 'header_translations' file.*
</div>

* missing columns = <span  class="redStar">**`r paste(.QC$thisStudy$missing.Columns,collapse = ' | ')`**</span>

<br/>


<h4 class="header2">Column report</h4>

`r b <- t(data.frame('CHR' = c(abs(study$column.NA.list$CHR - study$column.INVALID.list$CHR) ,
                              paste(study$column.INVALID.list$CHR, kableExtra::footnote_marker_symbol(6)),
                              ' '),

                    'POSITION' = c(abs(study$column.NA.list$POSITION - study$column.INVALID.list$POSITION) ,
                                   paste(study$column.INVALID.list$POSITION, kableExtra::footnote_marker_symbol(1), kableExtra::footnote_marker_symbol(2)),
                                   ' '),

                    'EFFECT_ALL' = c(abs(study$column.NA.list$EFFECT_ALL - study$column.INVALID.list$EFFECT_ALL) ,
                                     study$column.INVALID.list$EFFECT_ALL,
                                     ' '),

                    'OTHER_ALL' = c(abs(study$column.NA.list$OTHER_ALL - study$column.INVALID.list$OTHER_ALL) ,
                                    study$column.INVALID.list$OTHER_ALL,
                                    ' '),

                    'EFFECT' = c(abs(study$column.NA.list$EFFECT - study$column.INVALID.list$EFFECT) ,
                                 ' ',
                                 ' '),

                    'STDERR' = c(abs(study$column.NA.list$STDERR - study$column.INVALID.list$STDERR - study$column.INVALID.list$zero.STDERR) ,
                                 paste(study$column.INVALID.list$STDERR,kableExtra::footnote_marker_symbol(1)),
                                 paste(study$column.INVALID.list$zero.STDERR,kableExtra::footnote_marker_symbol(2))),

                    'EFF_ALL_FREQ' = c(abs(study$column.NA.list$EFF_ALL_FREQ - study$column.INVALID.list$EFF_ALL_FREQ - study$column.INVALID.list$minusone.EFF_ALL_FREQ),                                       paste(study$column.INVALID.list$EFF_ALL_FREQ,kableExtra::footnote_marker_symbol(1),kableExtra::footnote_marker_symbol(4)),
                                       paste(study$column.INVALID.list$minusone.EFF_ALL_FREQ,kableExtra::footnote_marker_symbol(3))),

                    'HWE_PVAL' = c(abs(study$column.NA.list$HWE_PVAL - study$column.INVALID.list$HWE_PVAL - study$column.INVALID.list$minusone.HWE_PVAL) ,
                                   paste(study$column.INVALID.list$HWE_PVAL,
                                         kableExtra::footnote_marker_symbol(1),
                                         kableExtra::footnote_marker_symbol(2),
                                         kableExtra::footnote_marker_symbol(4)),
                                  paste(study$column.INVALID.list$minusone.HWE_PVAL,
                                        kableExtra::footnote_marker_symbol(3))),

                    'PVALUE' = c(abs(study$column.NA.list$PVALUE - study$column.INVALID.list$PVALUE - study$column.INVALID.list$minusone.PVALUE) ,
                                 paste(study$column.INVALID.list$PVALUE,kableExtra::footnote_marker_symbol(1),kableExtra::footnote_marker_symbol(2),kableExtra::footnote_marker_symbol(4)),
                                 paste(study$column.INVALID.list$minusone.PVALUE,kableExtra::footnote_marker_symbol(3))),

                    'IMPUTED' = c(abs(study$column.NA.list$IMPUTED - study$column.INVALID.list$IMPUTED),
                                  study$column.INVALID.list$IMPUTED,
                                  ' '),

                    'IMP_QUALITY' = c(abs(study$column.NA.list$IMP_QUALITY - study$column.INVALID.list$IMP_QUALITY) ,
                                      paste(study$column.INVALID.list$IMP_QUALITY,kableExtra::footnote_marker_symbol(5)),
                                      ' '),

                    'MARKER' = c(abs(study$column.NA.list$MARKER - study$column.INVALID.list$MARKER) ,
                                ' ',
                                 ' '),

                    'N_TOTAL' = c(abs(study$column.NA.list$N_TOTAL - study$column.INVALID.list$N_TOTAL) ,
                                  paste(study$column.INVALID.list$N_TOTAL,
                                        kableExtra::footnote_marker_symbol(1),
                                        kableExtra::footnote_marker_symbol(2)),
                                  ' '),

                    'STRAND' = c(abs(study$column.NA.list$STRAND - study$column.INVALID.list$STRAND) ,
                                 study$column.INVALID.list$STRAND,
                                 ' '),

                    'CALLRATE' = c(abs(study$column.NA.list$CALLRATE - study$column.INVALID.list$CALLRATE - study$column.INVALID.list$minusone.CALLRATE),
                                   paste(study$column.INVALID.list$CALLRATE,
                                         kableExtra::footnote_marker_symbol(1),
                                         kableExtra::footnote_marker_symbol(4)),
                                   paste(study$column.INVALID.list$minusone.CALLRATE,
                                         kableExtra::footnote_marker_symbol(3)))


  ))

colnames(b) <- c('NA values','Invalid values','Uncertain values')

kable(b, align = "c", escape= FALSE ,format = "html") %>% 
kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
full_width = F, 
position = "left") %>%
kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
kableExtra::column_spec(2, width = "15em", border_right = T )  %>%
kableExtra::column_spec(3, width = "15em", border_right = T ) %>%
	kableExtra::footnote(general = ' ', symbol = c( 
                      "< 0",
                      "= 0",
                      "= -1",
                      "> 1",
                      sprintf("valid range is between %s and %s",.QC$config$filters$minimal_impQ_value,.QC$config$filters$maximal_impQ_value),
                      "valid range is between 1 and 26"))

`







<h4 class="header2">Variant processing</h4>


`r count.table <- t(data.table(
    "input variant count" = format(.QC$thisStudy$input.data.rowcount, big.mark="," , scientific = FALSE),
    "<span class='item'>Missing crucial variable</span>" = calculatePercent(.QC$thisStudy$missing.crucial.rowcount,
                                                  .QC$thisStudy$input.data.rowcount,
                                                  pretty = T),
    "<span class='item'>Duplicated variants</span>" = calculatePercent(.QC$thisStudy$duplicate.count,
                                             .QC$thisStudy$input.data.rowcount,
                                             pretty = T),
    "variant count after step 1"= calculatePercent(.QC$thisStudy$rowcount.step1,
                                                     .QC$thisStudy$input.data.rowcount,
                                                     decimal.place=3,
                                                     pretty = T),
    "<span class='item'>Monomorphic variants</span>" = calculatePercent(.QC$thisStudy$monomorphic.count,
                                              .QC$thisStudy$input.data.rowcount,
                                              pretty = T)))											


  colnames(count.table) <- 'Count'
  rownames(count.table)[1] <- "<span class='mainItem'>Input variant count</span>"
  rownames(count.table)[4] <- sprintf("<span class='mainItem'>Variant count after step 1 %s</span>",kableExtra::footnote_marker_symbol(1))
  
  
  
  if (.QC$thisStudy$x.chr.count.removed > 0) 
	count.table <- rbind(count.table, t(data.table("<span class='item'>Removed X variants</span>" = calculatePercent(.QC$thisStudy$x.chr.count.removed,
                                                                                                       .QC$thisStudy$input.data.rowcount,
                                                                                                       pretty = T))))
																									   
if (.QC$thisStudy$y.chr.count.removed > 0) 
	count.table <- rbind(count.table, t(data.table("<span class='item'>Removed Y variants</span>" = calculatePercent(.QC$thisStudy$y.chr.count.removed,
                                                                                                       .QC$thisStudy$input.data.rowcount,
                                                                                                       pretty = T))))
if (.QC$thisStudy$xy.chr.count.removed > 0) 
	count.table <- rbind(count.table, t(data.table("<span class='item'>Removed XY variants</span>" = calculatePercent(.QC$thisStudy$xy.chr.count.removed,
                                                                                                       .QC$thisStudy$input.data.rowcount,
                                                                                                       pretty = T))))
if (.QC$thisStudy$m.chr.count.removed > 0) 
	count.table <- rbind(count.table, t(data.table("<span class='item'>Removed M variants</span>" = calculatePercent(.QC$thisStudy$m.chr.count.removed,
                                                                                                       .QC$thisStudy$input.data.rowcount,
                                                                                                       pretty = T))))																									   
count.table2 <- t(data.table(
      "variant count after step 2" = calculatePercent(.QC$thisStudy$rowcount.step2,
                                                      .QC$thisStudy$input.data.rowcount,
                                                      decimal.place=3,
                                                      pretty = T),
    "variant count after step 3"= calculatePercent(.QC$thisStudy$rowcount.step3,
                                                       .QC$thisStudy$input.data.rowcount,
                                                       decimal.place=3,
                                                       pretty = T)))
											 
		

  rownames(count.table2)[1] <- sprintf("<span class='mainItem'>Variant count after step 2 %s</span>",kableExtra::footnote_marker_symbol(2))
  rownames(count.table2)[2] <- sprintf("<span class='mainItem'>Variant count after step 3 %s</span>",kableExtra::footnote_marker_symbol(3))

  count.table <- rbind(count.table,count.table2)
  
  kable(count.table,escape='FALSE', align = "l",format = "html") %>% 
	kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
	full_width = F, 
	position = "left") %>%
	kableExtra::column_spec(1, bold = F, border_right = T  )  %>%
	kableExtra::footnote(general = ' ', symbol = c( 
                      "step1: removing variants with missing crucial values and duplicated lines.",
                      "step2: removing monomorphic variants and specified chromosomes.",
                      "step3: removing mismatched, ambiguous and multi-allelic variants that could not be verified."))
					  
					  

`




<span class = 'important'>All further reports are based on variants after step3 (which will be saved as output file).</span>


<h3 class="header1">Description of variants</h3>


<br/>

<span class='mainItem'>Negative strand variants</span> : **`r .QC$thisStudy$neg.strand.count`**


<span class='mainItem'>Allele frequency = 0</span> : **`r .QC$thisStudy$column.INVALID.list$zero.EFF_ALL_FREQ`**


<span class='mainItem'>Allele frequency = 1</span> : **`r .QC$thisStudy$column.INVALID.list$one.EFF_ALL_FREQ`**




<br/>


`r count.table <- t(data.table(
    "<span class='mainItem'>High Quality variants</span>" = calculatePercent(.QC$thisStudy$HQ.count,
                                               .QC$thisStudy$rowcount.step3,
                                               pretty = T),
    "<span class='mainItem'>Low Quality variants</span>" = calculatePercent(.QC$thisStudy$LQ.count,
                                              .QC$thisStudy$rowcount.step3,
                                              pretty = T),
    "<span class='mainItem'>Palindromic variants*</span>" = calculatePercent(.QC$thisStudy$palindromic.rows,
                                              .QC$thisStudy$rowcount.step3,
                                              pretty = T),
    "<span class='mainItem'>Non-Palindromic variants</span>" = calculatePercent(.QC$thisStudy$non.palindromic.rows,
                                                  .QC$thisStudy$rowcount.step3,
                                                  pretty = T),
    "<span class='mainItem'>Palindromic variants with high allele frequency difference (> 0.15)</span>" = calculatePercent(.QC$thisStudy$palindormicHighDiffEAF,
                                    .QC$thisStudy$palindromic.rows,
                                    pretty = T),
	"<span class='mainItem'>Non-palindromic variants with high allele frequency difference (> 0.15)</span>" = calculatePercent(.QC$thisStudy$nonpalindormicHighDiffEAF ,
                                      .QC$thisStudy$non.palindromic.rows,
                                      pretty = T),
    "<span class='mainItem'>Palindromic variants with opposite allele frequency \"compared to the reference\" (> 0.65 for the input file and < 0.35 for the reference, or vice versa)</span>" =  calculatePercent(.QC$thisStudy$palindormicExtremeDiffEAF ,
                                      .QC$thisStudy$palindromic.rows,
                                      pretty = T)))

  colnames(count.table) <- 'Count'
  
	kable(count.table,escape='FALSE', align = "l",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T, width= "40em")%>%
		kableExtra::footnote(general = ' ', symbol = c( 
                      "Palindromic variants are variants with strand-independent allele-configurations (A/T and C/G)"))
`

<br/>
<span class='mainItem'>Imputation status</span>
`r tbl = .QC$thisStudy$tables$imputed.tbl

colnames(tbl) <- c('','Count')


kable(tbl, align = "c",format = "html") %>% 
kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
full_width = F, 
position = "left") %>%
kableExtra::column_spec(1, bold = T, border_right = T ,width = "15em" ) %>%
kableExtra::column_spec(2, width = "10em")

`


<br/>


<span class='mainItem'>Variant count for each chromosome</span>
`r 

if(!is.na(study$tables$CHR.tbl))
  {
	tbl = t(.QC$thisStudy$tables$CHR.tbl)
	rownames(tbl) <- c('Chromosome','Count')


	kable(tbl, align = "c",format = "html") %>% 
	kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
	full_width = F, 
	position = "left") %>%
	kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
	kableExtra::column_spec(2, width = "10em") %>%
	kableExtra::scroll_box(width = "100%", height = "80%")
	} else{ paste('CHR column not found!')}
`

`r 
if(length(study$missing_chromosomes) >0 )
sprintf('* Missing chromosome(s) number <span  class="redStar">**%s**</span>', paste(.QC$thisStudy$missing_chromosomes,collapse = ', '))

`

<br/>


<h3 class="header1">Result from matching variants with reference datasets</h3>


<h4 class="header2">Variant types after matching with standard reference datasets</h4>

`r 
if(nrow(.QC$thisStudy$tables$multi_allele_count_preProcess) > 1)
  kable(.QC$thisStudy$tables$multi_allele_count_preProcess,escape='FALSE', align = "l",format = "html") %>% 
  		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
  		full_width = F, 
  		position = "left") %>%
  		kableExtra::column_spec(1, bold = T, border_right = T)
`

 <h4 class="header2">Result of matching with standard reference dataset</h4>

 
`r  count.table1 <- t(data.table(
    "<span class='mainItem'>Verified variants</span>" = calculatePercent(.QC$thisStudy$found.rows.std,
                                        .QC$thisStudy$rowcount.step2,
                                        decimal.place=3,
                                        pretty=TRUE),
    "<span class='mainItem'>Not-found variants</span>" = calculatePercent(.QC$thisStudy$not.found.rows.std,
                                            .QC$thisStudy$rowcount.step2,
                                            decimal.place=3,
                                            pretty=TRUE),
    "<span class='mainItem'>Flipped variants</span>" = calculatePercent(.QC$thisStudy$flipped.rows.std,
                                          .QC$thisStudy$found.rows.std,
                                          pretty=TRUE),
    "<span class='mainItem'>Switched variants</span>" = calculatePercent(.QC$thisStudy$switched.rows.std,
                                           .QC$thisStudy$found.rows.std,
                                           pretty=TRUE),
    "<span class='mainItem'>Allele frequency correlation</span>" = '',
    "<span class='item'>r (all variants)</span>" = .QC$thisStudy$AFcor.std_ref,
    "<span class='item'>r (palindromic)</span>" = .QC$thisStudy$AFcor.palindromic.std_ref,
    "<span class='item'>r (non-palindromic)</span>" = .QC$thisStudy$AFcor.non.palindromic.std_ref,
	"<span class='item'>r (INDEL)</span>" = .QC$thisStudy$AFcor.std_ref.indel))

  colnames(count.table1) <- 'Count'
  kable(count.table1,escape='FALSE', align = "c",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em") %>%
		kableExtra::column_spec(2, width="10em")
`

<br/>


`r 
if(file.exists(.QC$thisStudy$stdMafPlotPath) & .QC$graphic.device != 'tiff')
{
paste(' <h4 class="header2">Standard reference allele-frequency comparison plot</h4>')
	htmltools::img(src = knitr::image_uri(.QC$thisStudy$stdMafPlotPath), 
               alt = 'MAF', 
               style = 'width:100%')
}
`



***




`r if(!is.na(.QC$config$supplementaryFiles$allele_ref_alt))
  paste('<h4 class="header2">Result of matching with alternative reference dataset</h4>')
`

`r if(!is.na(.QC$config$supplementaryFiles$allele_ref_alt)){
 
 count.table2 <- t(data.table(
      "<span class='mainItem'>Verified variants</span>" = calculatePercent(.QC$thisStudy$found.rows.alt ,
                                          .QC$thisStudy$not.found.rows.std,
                                          decimal.place=3,
                                          pretty=TRUE),
      "<span class='mainItem'>Not-found variants</span>" = calculatePercent(.QC$thisStudy$not.found.rows.alt ,
                                              .QC$thisStudy$not.found.rows.std,
                                              decimal.place=3,
                                              pretty=TRUE),
      "<span class='mainItem'>Flipped variants</span>" = calculatePercent(.QC$thisStudy$flipped.rows.alt ,
                                            .QC$thisStudy$found.rows.alt,
                                            pretty=TRUE),
      "<span class='mainItem'>Switched variants</span>" = calculatePercent(.QC$thisStudy$switched.rows.alt ,
                                             .QC$thisStudy$found.rows.alt,
                                             pretty=TRUE),
      "<span class='mainItem'>Allele frequency correlation</span>" = '',
      "<span class='item'>r (all variants)</span>" = .QC$thisStudy$AFcor.alt_ref,
      "<span class='item'>r (palindromic)</span>" = .QC$thisStudy$AFcor.palindromic.alt_ref,
      "<span class='item'>r (non-palindromic)</span>" = .QC$thisStudy$AFcor.non.palindromic.alt_ref))

    colnames(count.table2) <- 'Count'
	
	  kable(count.table2,escape='FALSE', align = "c",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em") %>%
		kableExtra::column_spec(2, width="10em")	
 }
`

<br/>


`r 
if(file.exists(.QC$thisStudy$altMafPlotPath) & .QC$graphic.device != 'tiff')
{
paste(' <h4 class="header2">Standard reference allele-frequency comparison plot</h4>')
	htmltools::img(src = knitr::image_uri(.QC$thisStudy$altMafPlotPath), 
               alt = 'MAF', 
               style = 'width:100%')
}
`


<h3 class="header1">QC summary statistics</h3>


  

 <h4 class="header2">P-value correlation (observed vs expected)</h4>
 <div><strong>Note:</strong> Only variants with a valid P-value are used for P-value correlation calculation.</div>
  `r  count.table1 <- t(data.table(
    "<span class='mainItem'>Included variants</span>" = calculatePercent(.QC$thisStudy$rownum.PVcor,
                                           .QC$thisStudy$rowcount.step3,
                                           pretty = T),
    "<span class='item'>r</span>" = .QC$thisStudy$PVcor))
	
	  colnames(count.table1) <- 'Value'  
    
  kable(count.table1,escape='FALSE', align = "c",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em") %>%
		kableExtra::column_spec(2, width="10em")
`


<br/>

`r 
if(file.exists(.QC$thisStudy$pvalCorPlotPath) & .QC$graphic.device != 'tiff')
{
  paste('<h4 class="header2">P-value correlation plot</h4>')

  if(.QC$thisStudy$PVcor > 0.95)
  {
  	htmltools::img(src = knitr::image_uri(.QC$thisStudy$pvalCorPlotPath), 
                 alt = 'MAF', 
                 style = 'width:50%')
  }
  else
  {
  	htmltools::img(src = knitr::image_uri(.QC$thisStudy$pvalCorPlotPath), 
                 alt = 'MAF', 
                 style = 'width:100%')
  }
}
`

***


 <h4 class="header2">Distribution statistics [1]</h4>

`r 	count.table2 <- t(data.table(
    "<span class='mainItem'>Skewness</span>" = .QC$thisStudy$skewness,
    "<span class='mainItem'>Skewness (HQ)</span>" = .QC$thisStudy$skewness.HQ,
    "<span class='mainItem'>Kurtosis</span>" = .QC$thisStudy$kurtosis,
    "<span class='mainItem'>Kurtosis (HQ)</span>" = .QC$thisStudy$kurtosis.HQ,
    "<span class='mainItem'>Visscher's stat</span>" = .QC$thisStudy$Visschers.stat ,
    "<span class='mainItem'>Visscher's stat (HQ)</span>" = .QC$thisStudy$Visschers.stat.HQ,
    "<span class='mainItem'>Lambda - total</span>" = .QC$thisStudy$lambda ,
    "<span class='mainItem'>Lambda - genotyped</span>" = .QC$thisStudy$lambda.gen,
    "<span class='mainItem'>Lambda - imputed</span>" = .QC$thisStudy$lambda.imp,
	"<span class='mainItem'>Sample Size (max)</span>" = .QC$thisStudy$MAX_N_TOTAL,
    "<span class='mainItem'>Fixed HWE P-value</span>" = .QC$thisStudy$fixed.hwep,
    "<span class='mainItem'>Fixed Imputation Quality</span>" = .QC$thisStudy$fixed.impq,
    "<span class='mainItem'>Fixed Call Rate</span>" = .QC$thisStudy$fixed.callrate,
    "<span class='mainItem'>Fixed Sample Size</span>" = .QC$thisStudy$fixed.n_total))
	
	  colnames(count.table2) <- 'Value'
	 		
		kable(count.table2,escape='FALSE', align = "c",format = "html") %>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em") %>%
		kableExtra::column_spec(2, width="10em") %>%
		kableExtra::footnote(general = ' ', symbol = c( 
                      "**HQ** = High-Quality variants"))
`

***
 <h4 class="header2">Distribution statistics [2]</h4>
 
 <h5>All variants</h5>
`r 
kable(t(.QC$thisStudy$tables$variable.summary), format = "html")%>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em")
`


`r if(nrow(.QC$thisStudy$tables$variable.summary.HQ ) > 0 & .QC$thisStudy$HQ.count != .QC$thisStudy$rowcount.step3){ 
      paste('<hr/><h5>HQ variants</h5>')
}
`


`r if(nrow(.QC$thisStudy$tables$variable.summary.HQ ) > 0 & .QC$thisStudy$HQ.count != .QC$thisStudy$rowcount.step3)
  {
    kable(t(.QC$thisStudy$tables$variable.summary.HQ), format = "html")%>% 
		kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "condensed", "responsive"), 
		full_width = F, 
		position = "left") %>%
		kableExtra::column_spec(1, bold = T, border_right = T,width="15em")
  }
`





<h4 class="header2">Effect allele distribution in SNP variants</h4>
`r 

tbl = merge(.QC$thisStudy$tables$EFFECT_ALL.tbl,
.QC$thisStudy$tables$EFFECT_ALL.post.matching.tbl,
by="EFFECT_ALL",
all = T)
tbl = t(tbl)

rownames(tbl) <- c('Allele','Count (input file)','Count (post-matching)')

kable(tbl, align = "c",format = "html") %>%
kableExtra::kable_styling(bootstrap_options = c("striped", "hover",  "responsive"),
full_width = F,
position = "left") %>%
kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
kableExtra::column_spec(2, width = "10em")`




<h4 class="header2">Other allele distribution in SNP variants</h4>
`r 

tbl = merge(.QC$thisStudy$tables$OTHER_ALL.tbl,
.QC$thisStudy$tables$OTHER_ALL.post.matching.tbl,
by="OTHER_ALL",
all = T)
tbl = t(tbl)

rownames(tbl) <- c('Allele','Count (input file)','Count (post-matching)')

kable(tbl, align = "c",format = "html") %>%
kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "responsive"),
full_width = F,
position = "left") %>%
kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
kableExtra::column_spec(2, width = "10em")`



`r if(!is.null(.QC$thisStudy$tables$betaCor.tbl)  & !is.na(.QC$config$supplementaryFiles$beta_ref_std)){ 
      paste('<h3 class="header1">Effect-size correlation</h3>')
}
`

`r if(!is.null(.QC$thisStudy$tables$betaCor.tbl)  & !is.na(.QC$config$supplementaryFiles$beta_ref_std)){ 
      kable(.QC$thisStudy$tables$betaCor.tbl, align = "c",format = "html") %>%
      kableExtra::kable_styling(bootstrap_options = c("striped", "hover", "responsive"),
      full_width = F,
      position = "left") %>%
      kableExtra::column_spec(1, bold = T, border_right = T  ) %>%
      kableExtra::column_spec(2, width = "10em")%>%
		  kableExtra::footnote(general = c(  
                      "* = Data is presented as r(N). Variants were filtered on reference data P-values.",
                      "** = Data is presented as r(N). Variants were filtered on input result file P-values."))
			}
`


`r 
if(!is.null(.QC$thisStudy$tables$betaCor.tbl)  & file.exists(.QC$thisStudy$effPlotPath) & .QC$graphic.device != 'tiff')
{

	htmltools::img(src = knitr::image_uri(.QC$thisStudy$effPlotPath), 
               alt = 'MAF', 
               style = 'width:50%')
}

`





`r if(file.exists(.QC$thisStudy$histPlotPath) & .QC$graphic.device != 'tiff')
  paste('<h3 class="header1">Plots</h3>')
`



`r 
if(file.exists(.QC$thisStudy$histPlotPath) & .QC$graphic.device != 'tiff')
{
	htmltools::img(src = knitr::image_uri(.QC$thisStudy$histPlotPath), 
               alt = 'MAF', 
               style = 'width:100%')
}
`


***


`r 
if(file.exists(.QC$thisStudy$QQPlotPath) & .QC$graphic.device != 'tiff'){
	htmltools::img(src = knitr::image_uri(.QC$thisStudy$QQPlotPath), 
               alt = 'MAF', 
               style = 'width:100%')
}

`

***

`r 
if(file.exists(.QC$thisStudy$manPlotPath) & .QC$graphic.device != 'tiff')
{
	htmltools::img(src = knitr::image_uri(.QC$thisStudy$manPlotPath), 
               alt = 'MAF', 
               style = 'width:100%')
}

`
