Analysis_R_Scripts/HPRC_ATACseq/ComparePeaks.Rmd

---
title: "ATAC-seq peak comparison analysis"
author: "CIG @ MGI"
date: "`r Sys.Date()`"
output: html_document
---

```{r setup, include=FALSE}
knitr::opts_chunk$set(echo = TRUE)
knitr::opts_knit$set(root.dir = "/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/PeakComparison/")

# Set seed
set.seed(0)

# Load packages
library(ggplot2)
require(cowplot)
library(viridis)
library(tidyr)
library(dplyr)
library(ggpubr)

theme_set(theme_cowplot())

source("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Misc_Code/CS_Aesthetic.R")
```

```{r Import peak information}
All_Original<-read.delim("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/PeakComparison/ClusterPeaks/All_Combined_Peaks.txt", header = FALSE)
colnames(All_Original)<-c("Chromosome","Start","Stop","Name","Score","Strand","SignalValue","pValue","qValue","Peak")

# Read in pre-lift over data
All_Original_Query<-read.delim("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/PeakComparison/ClusterPeaks/All_Original_Query_peaks.narrowPeak", header = FALSE)
colnames(All_Original_Query)<-c("Chromosome","Start","Stop","Name","Score","Strand","SignalValue","pValue","qValue","PeakPosition")

All_Original$Run<-unlist(lapply(
  1:nrow(All_Original),
  function(INDEX) paste(strsplit(All_Original$Name[INDEX],split = "_")[[1]][c(3,4,5)],collapse = "_")
  ))

# subset out non-main chromosome peaks {chr1-chr22, chrX, chrY} specific to pan-genome
NonMainChromosome<-subset(All_Original, !(Chromosome %in% c("chr1","chr2","chr3","chr4","chr5","chr6","chr7","chr8","chr9","chr10","chr11","chr12","chr13","chr14","chr15","chr16","chr17","chr18","chr19","chr20","chr21","chr22","chrX","chrY","FAILEDLIFT")))
print(nrow(NonMainChromosome))

All_Original<-subset(All_Original, Chromosome %in% c("chr1","chr2","chr3","chr4","chr5","chr6","chr7","chr8","chr9","chr10","chr11","chr12","chr13","chr14","chr15","chr16","chr17","chr18","chr19","chr20","chr21","chr22","chrX","chrY","FAILEDLIFT"))

```

```{r How many peaks are called?, include=TRUE}
RunTable<-data.frame(table(All_Original$Run))

RunNumberOfPeaks<-data.frame(
Sample=unlist(lapply(as.character(RunTable$Var1), function(RUN) strsplit(RUN, split = "_")[[1]][1] )),
Replicate=unlist(lapply(as.character(RunTable$Var1), function(RUN) strsplit(RUN, split = "_")[[1]][2] )),
Genome=unlist(lapply(as.character(RunTable$Var1), function(RUN) strsplit(RUN, split = "_")[[1]][3] )),
NumberOfPeaks=RunTable$Freq
)

RunNumberOfPeaks$Genome[RunNumberOfPeaks$Genome %in% c("HG00621.maternal","HG00741.maternal","HG01952.maternal","HG01978.maternal","HG03516.maternal")]<-"Maternal"
RunNumberOfPeaks$Genome[RunNumberOfPeaks$Genome %in% c("HG00621.paternal.wMito","HG00741.paternal.wMito","HG01952.paternal.wMito","HG01978.paternal.wMito","HG03516.paternal.wMito")]<-"Paternal"
RunNumberOfPeaks$Genome[RunNumberOfPeaks$Genome == "hg38.LOCAL"]<-"hg38"
RunNumberOfPeaks$Genome[RunNumberOfPeaks$Genome == "pangenome.hg38"]<-"pangenome"

RunNumberOfPeaks
```

```{r Plot number of peaks called, fig.width=18, fig.height=4}
All_Original$LiftsOver<-All_Original$Chromosome!="FAILEDLIFT"
All_Original$LiftsOver[All_Original$LiftsOver==TRUE]<-"Yes"
All_Original$LiftsOver[All_Original$LiftsOver==FALSE]<-"No"
# Split Run field into Sample, Replicate, and Genome
All_Original$Sample<-unlist(lapply(as.character(All_Original$Run), function(RUN) strsplit(RUN, split = "_")[[1]][1] ))
All_Original$Replicate<-unlist(lapply(as.character(All_Original$Run), function(RUN) strsplit(RUN, split = "_")[[1]][2] ))
All_Original$Genome<-unlist(lapply(as.character(All_Original$Run), function(RUN) strsplit(RUN, split = "_")[[1]][3] ))

# Rename
All_Original$Genome[All_Original$Genome %in% c("HG00621.maternal","HG00741.maternal","HG01952.maternal","HG01978.maternal","HG03516.maternal")]<-"Maternal"
All_Original$Genome[All_Original$Genome %in% c("HG00621.paternal.wMito","HG00741.paternal.wMito","HG01952.paternal.wMito","HG01978.paternal.wMito","HG03516.paternal.wMito")]<-"Paternal"
All_Original$Genome[All_Original$Genome == "pangenome.hg38"]<-"pangenome"

# Add the original name as a column
All_Original$Genome.OriginalName<-unlist(lapply(as.character(All_Original$Run), function(RUN) strsplit(RUN, split = "_")[[1]][3] ))

PlotPeakCounts<-ggplot(subset(RunNumberOfPeaks, Genome != "hg38.NoBlackList"),aes(x=Genome, y=NumberOfPeaks/1000, fill=Replicate))+
  geom_bar(stat="identity", position = position_dodge())+
  ylab("Number of peaks (K)")+
  CS.THEME+
  scale_y_continuous(expand = c(0,0),limits = c(0,125))+
  facet_grid(~Sample)+
  theme(axis.text.x = element_text(angle = 30,hjust=1))+
  scale_fill_manual(values = c(CS.ColorPalette[11,1],CS.ColorPalette[12,1]))

ggsave2(filename = "PlotPeakCounts.png",plot = PlotPeakCounts, units = "in", width = 18, height = 4)
PlotPeakCounts
```

```{r Which peaks can lift over?, include=FALSE}
as.data.frame(subset(All_Original, LiftsOver=="Yes")$Name)->List_All_LiftedOver_Peak_Names 
colnames(List_All_LiftedOver_Peak_Names)<-"Peak"
```

```{r Which peaks cannot lift over?, include=FALSE}
as.data.frame(subset(All_Original, LiftsOver=="No")$Name)->List_All_CannotLiftOver_Peak_Names
colnames(List_All_CannotLiftOver_Peak_Names)<-"Peak"
```

```{r Check for shenanigans, include=TRUE}
#if there are no shenanigans these should all return 0
sum(List_All_LiftedOver_Peak_Names$Peak %in% List_All_CannotLiftOver_Peak_Names$Peak)
sum(List_All_CannotLiftOver_Peak_Names$Peak %in% List_All_LiftedOver_Peak_Names$Peak)
sum(!(List_All_LiftedOver_Peak_Names$Peak %in% All_Original$Name))
sum(!(List_All_CannotLiftOver_Peak_Names$Peak %in% All_Original$Name))
```
```{r list all runs, include=TRUE}
unique(All_Original$Run)
table(All_Original$LiftsOver)
```

```{r plot number of peaks that can lift over, fig.width=18, fig.height=4}
PlotPeakCountsCannotLiftOver<-ggplot(subset(All_Original,LiftsOver=="No"),aes(x=Genome, fill=Replicate))+
  geom_bar(stat = 'count', position = position_dodge())+
  ylab("Number of peaks\n cannot lift over")+
  CS.THEME+
  scale_y_continuous(expand = c(0,0),limits = c(0,500))+
  theme(axis.text.x = element_text(angle = 30,hjust=1))+
  facet_grid(~Sample)+
  scale_fill_manual(values = c(CS.ColorPalette[11,1],CS.ColorPalette[12,1]))

ggsave2(filename = "PlotPeakCountsCannotLiftOver.png",plot = PlotPeakCountsCannotLiftOver, units = "in", width = 18, height = 4)
PlotPeakCountsCannotLiftOver
```

```{r prepare preak threshold data, include=FALSE}
# Define buildThresholdedPeakCountsDataframes function
buildThresholdedPeakCountsDataframes<-function(THRESHOLDS.LIST,SAMPLE,REPLICATE,GENOME,LIFTSOVER){
  DATA<-lapply(
    THRESHOLDS.LIST,
    function(THRESHOLD) data.frame( Threshold=THRESHOLD, Count=nrow(subset(All_Original, Sample==SAMPLE & Replicate==REPLICATE & Genome==GENOME & LiftsOver %in% LIFTSOVER & SignalValue > THRESHOLD)) )
  ) %>% bind_rows()
  
  ## & LiftsOver %in% LIFTSOVER
  DATA$Percent<-DATA$Count/nrow(subset(All_Original, Sample==SAMPLE & Replicate==REPLICATE & Genome==GENOME ))
  DATA$Sample<-SAMPLE
  DATA$Replicate<-REPLICATE
  DATA$Genome<-GENOME
  DATA$LiftsOver<-LIFTSOVER
  return(DATA)
}

ListOfThresholds<-c(1,2,4,8,16,32)

PeakThresholdBreadown<-lapply(
  unique(All_Original$Sample),
  function(SAMPLE) rbind(
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","hg38.LOCAL","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","Maternal","Yes" ),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","Paternal","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","CHM13","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","pangenome","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","Maternal","No" ),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","Paternal","No"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"A","CHM13","No"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","hg38.LOCAL","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","Maternal","Yes" ),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","Paternal","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","CHM13","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","pangenome","Yes"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","Maternal","No" ),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","Paternal","No"),
    buildThresholdedPeakCountsDataframes(ListOfThresholds,SAMPLE,"B","CHM13","No")
  )
) %>% bind_rows()


PeakThresholdBreadown$Genome[PeakThresholdBreadown$Genome=="hg38.LOCAL"]<-"hg38"
```

```{r build thresholding plots, include=FALSE}
ThresholdBreakdown.plot.A<-ggplot(subset(PeakThresholdBreadown, LiftsOver=="Yes") ,aes(x=as.factor(Threshold),y=Count,fill=Genome))+
  geom_bar(stat = "identity", position = position_dodge())+
  facet_grid(Replicate~Sample)+
  CS.THEME+
  scale_fill_manual(values = CS.ColorPalette[c(28,7,20,4,26),1])+
  xlab("Signal value threshold")+
  ylab("Number of peaks above threshold")+
  ggtitle("Breakdown of peaks:\nCan lift over to hg38")

ThresholdBreakdown.plot.B<-ggplot(subset(PeakThresholdBreadown, LiftsOver=="No") ,aes(x=as.factor(Threshold),y=Count,fill=Genome))+
  geom_bar(stat = "identity", position = position_dodge())+
  facet_grid(Replicate~Sample)+
  CS.THEME+
  scale_fill_manual(values = CS.ColorPalette[c(28,20,4,26),1])+
  xlab("Signal value threshold")+
  ylab("Number of peaks above threshold")+
  ggtitle("Breakdown of peaks:\nCannot lift over to hg38")


ThresholdBreakdown.panel<-plot_grid(ThresholdBreakdown.plot.A,ThresholdBreakdown.plot.B, ncol=1)

ggsave2(filename = "ThresholdBreakdown.panel.png",plot = ThresholdBreakdown.panel,units = "in", height = 12, width = 12)
```

```{r build volcano plot, include=TRUE, fig.width=12, fig.height=12}
PeakVolcano.plot<-ggplot(All_Original, aes(x=SignalValue,y=qValue, color=Replicate) )+
  geom_point(size=0.1, alpha=0.5)+
  geom_vline(xintercept = 8)+
  geom_hline(yintercept = -log10(0.001), color="red")+
  scale_y_continuous(trans = "log10")+
  facet_grid(Genome~Sample)+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "cividis", begin = 0.9, end = 0.1)

ggsave2(filename = "PeakVolcano.plot.png",plot = PeakVolcano.plot,units = "in", height = 12, width = 12)
PeakVolcano.plot
```

```{r filter peaks by signalValue, include=FALSE}
All_Original.Filtered<-subset(All_Original, SignalValue >=8)
```

```{r plot localization of peaks which cannot lift over, include=FALSE}
# filter peaks by signalValue
All_Original_Query<-subset(All_Original_Query, SignalValue >=8)
# Make Genome.OriginalName column
All_Original_Query$Genome.OriginalName<-unlist(lapply(as.character(All_Original_Query$Name), function(RUN) strsplit(RUN, split = "_")[[1]][5] ))
# Make LiftsOver column
All_Original_Query$LiftsOver<-All_Original_Query$Name %in% List_All_CannotLiftOver_Peak_Names$Peak
All_Original_Query$LiftsOver[All_Original_Query$LiftsOver==TRUE]<-"No"
All_Original_Query$LiftsOver[All_Original_Query$LiftsOver==FALSE]<-"Yes"
# Make Sample column
All_Original_Query$Sample<-unlist(lapply(as.character(All_Original_Query$Name), function(RUN) strsplit(RUN, split = "_")[[1]][3] ))


library(circlize)
# Import genome sizes
GenomeSizes<-read.delim("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/HPRC_General/GenomeLengths.csv",sep = ",")
GenomeSizes<-subset(GenomeSizes,Chromsome != "chrM")
GenomeSizes$Chromsome<-factor(GenomeSizes$Chromsome, levels = c("chr1","chr2","chr3","chr4","chr5","chr6","chr7","chr8","chr9","chr10","chr11","chr12","chr13","chr14","chr15","chr16","chr17","chr18","chr19","chr20","chr21","chr22","chrX","chrY"))


# Define plotting function
PlotLocationThatCannotLiftOver<-function(GENOME,GENOME.ORIGINAL,SAMPLE,FILENAME){
  df = data.frame(
    sectors = subset(All_Original_Query,Genome.OriginalName==GENOME.ORIGINAL & LiftsOver=="No" & Sample==SAMPLE)$Chromosome,
    x = subset(All_Original_Query,Genome.OriginalName==GENOME.ORIGINAL & LiftsOver=="No" & Sample==SAMPLE)$Start,
    y = subset(All_Original_Query,Genome.OriginalName==GENOME.ORIGINAL & LiftsOver=="No" & Sample==SAMPLE)$qValue
  )
  
  #print(unique(df$sectors))
  png(file = FILENAME, units = "in", width = 12, height = 12, res = 100)
  
  circos.par("track.height" = 0.2)
  circos.par(cell.padding = c(0.02, 0, 0.02, 0))
  
  GenomeSizes<-GenomeSizes[, colnames(GenomeSizes) %in% c("Chromsome",GENOME) ]
  GenomeSizes<-GenomeSizes[!is.na(GenomeSizes[,2]),]
  
  circos.initialize(c(GenomeSizes$Chromsome,GenomeSizes$Chromsome), x = c(GenomeSizes[,colnames(GenomeSizes)==GENOME], rep(0,length(GenomeSizes[,colnames(GenomeSizes)==GENOME]))))
  
  circos.track(df$sectors, y = df$y,
               panel.fun = function(x, y) {
                 circos.text(CELL_META$xcenter,
                             CELL_META$cell.ylim[2] + mm_y(5),
                             CELL_META$sector.index)
                 circos.axis(labels.cex = 0.05)
               },
               bg.col = viridis(24, alpha = 0.2),
  )
  
  
  circos.trackPoints(df$sectors, df$x, df$y, pch = 16, cex = 0.5)
  
  circos.par("track.height" = 0.3)
  circos.trackHist(df$sectors, df$x, bin.size = 1000000, bg.col = viridis(24, alpha = 0.2), col = NA)
  
  dev.off()
}

# Generate plots
PlotLocationThatCannotLiftOver("HG00621.paternal","HG00621.paternal.wMito","HG00621","CannotLiftOver_Locations_HG00621_Paternal.png")
PlotLocationThatCannotLiftOver("HG00621.maternal","HG00621.maternal","HG00621","CannotLiftOver_Locations_HG00621_Maternal.png")
PlotLocationThatCannotLiftOver("CHM13","CHM13","HG00621","CannotLiftOver_Locations_HG00621_CHM13.png")

PlotLocationThatCannotLiftOver("HG00741.paternal","HG00741.paternal.wMito","HG00741","CannotLiftOver_Locations_HG00741_Paternal.png")
PlotLocationThatCannotLiftOver("HG00741.maternal","HG00741.maternal","HG00741","CannotLiftOver_Locations_HG00741_Maternal.png")
PlotLocationThatCannotLiftOver("CHM13","CHM13","HG00741","CannotLiftOver_Locations_HG00741_CHM13.png")

PlotLocationThatCannotLiftOver("HG01952.paternal","HG01952.paternal.wMito","HG01952","CannotLiftOver_Locations_HG01952_Paternal.png")
PlotLocationThatCannotLiftOver("HG01952.maternal","HG01952.maternal","HG01952","CannotLiftOver_Locations_HG01952_Maternal.png")
PlotLocationThatCannotLiftOver("CHM13","CHM13","HG01952","CannotLiftOver_Locations_HG01952_CHM13.png")

PlotLocationThatCannotLiftOver("HG01978.paternal","HG01978.paternal.wMito","HG01978","CannotLiftOver_Locations_HG01978_Paternal.png")
PlotLocationThatCannotLiftOver("HG01978.maternal","HG01978.maternal","HG01978","CannotLiftOver_Locations_HG01978_Maternal.png")
PlotLocationThatCannotLiftOver("CHM13","CHM13","HG01978","CannotLiftOver_Locations_HG01978_CHM13.png")

PlotLocationThatCannotLiftOver("HG03516.paternal","HG03516.paternal.wMito","HG03516","CannotLiftOver_Locations_HG03516_Paternal.png")
PlotLocationThatCannotLiftOver("HG03516.maternal","HG03516.maternal","HG03516","CannotLiftOver_Locations_HG03516_Maternal.png")
PlotLocationThatCannotLiftOver("CHM13","CHM13","HG03516","CannotLiftOver_Locations_HG03516_CHM13.png")
```

```{r import peak cluster data, include=FALSE}
Clusters<-read.delim("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/PeakComparison/ClusterPeaks/PeakToClusterIntersect.txt",header = FALSE)
colnames(Clusters)<-c("Peak","Chromosome","Start","Stop")

Clusters$ClusterNumber<-unlist(lapply(1:nrow(Clusters), function(ROW) paste(Clusters[ROW,2],Clusters[ROW,3],Clusters[ROW,4], sep = "_") ))
```

```{r add cluster info to peaks, include=FALSE}
All_Original$Cluster<-Clusters$ClusterNumber[match(All_Original$Name,Clusters$Peak)]
All_Original.Filtered$Cluster<-Clusters$ClusterNumber[match(All_Original.Filtered$Name,Clusters$Peak)]

# For instances where the cluster is not found, use the peak name
All_Original$Cluster[is.na(All_Original$Cluster)]<-All_Original$Name[is.na(All_Original$Cluster)]
All_Original.Filtered$Cluster[is.na(All_Original.Filtered$Cluster)]<-All_Original.Filtered$Name[is.na(All_Original.Filtered$Cluster)]
```

```{r setup for upset plot, include=TRUE}
# Generate pre-upset datadrame. Exlcude hg38.NoBlackList
# Spread by genome and cluster
Sample.PreUpset.DF<-spread(unique(subset(All_Original.Filtered, Genome!="hg38.NoBlackList")[,c(13,14,12,17,15,17)]), Genome, Cluster)
colnames(Sample.PreUpset.DF)[colnames(Sample.PreUpset.DF)=="hg38.LOCAL"]<-"hg38"

# Make list of cluster names after filtering
ClusterNames<-Sample.PreUpset.DF$Cluster.1

# Remove the cluster column now that we have the names in a separate variable
#Sample.PreUpset.DF<-Sample.PreUpset.DF[,-4]

# Define list of genomes to compare
RunsToCompare<-colnames(Sample.PreUpset.DF)[5:9]

# For corresponding columns, if the value is NA, set to FALSE
Sample.PreUpset.DF[RunsToCompare] = !is.na(Sample.PreUpset.DF[RunsToCompare])

# Do the dimensions match? If not, there is a problem
print(length(ClusterNames)==nrow(Sample.PreUpset.DF))
```

```{r define upset plot function, include=TRUE}
library("ComplexUpset")

MakeUpsetPlot<-function(UPSET.DF,RUNSTOCOMPARE,LABEL){
  upset(
    UPSET.DF,
    RUNSTOCOMPARE,
    name=LABEL,
    width_ratio=0.1,
    set_sizes = FALSE,
    keep_empty_groups=TRUE,
    sort_sets=FALSE,
    sort_intersections_by=c('degree'),
    base_annotations=list(
      'Intersection size'=intersection_size(
        text_mapping=aes(
          label=paste0(
            round(
              !!get_size_mode('exclusive_intersection')/!!get_size_mode('inclusive_union') * 100,
              2
            ),
            '%'
          )                                                                                                  ),mapping=aes(fill=LiftsOver),text=list(
            vjust=-0.1,
            hjust=-0.1,
            angle=60,
            size=2.5
          )
      )+ scale_fill_manual(values=c('Yes'=CS.ColorPalette[11,1], 'No'=CS.ColorPalette[19,1]))
    )
  )+CS.THEME
}
```

```{r generate upset plots, include=FALSE}
# Generate individual upset plots
SampleUpsetPlot_HG00621_A<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG00621" & Replicate=="A"),
  RunsToCompare,
  'HG00621 A'
)

SampleUpsetPlot_HG00621_B<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG00621" & Replicate=="B"),
  RunsToCompare,
  'HG00621 B'
)

SampleUpsetPlot_HG00741_A<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG00741" & Replicate=="A"),
  RunsToCompare,
  'HG00741 A'
)

SampleUpsetPlot_HG00741_B<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG00741" & Replicate=="B"),
  RunsToCompare,
  'HG00741 B'
)

SampleUpsetPlot_HG01952_A<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG01952" & Replicate=="A"),
  RunsToCompare,
  'HG01952 A'
)

SampleUpsetPlot_HG01952_B<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG01952" & Replicate=="B"),
  RunsToCompare,
  'HG01952 B'
)

SampleUpsetPlot_HG01978_A<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG01978" & Replicate=="A"),
  RunsToCompare,
  'HG01978 A'
)

SampleUpsetPlot_HG01978_B<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG01978" & Replicate=="B"),
  RunsToCompare,
  'HG01978 B'
)

SampleUpsetPlot_HG03516_A<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG03516" & Replicate=="A"),
  RunsToCompare,
  'HG03516 A'
)

SampleUpsetPlot_HG03516_B<-MakeUpsetPlot(
  subset(Sample.PreUpset.DF,Sample=="HG03516" & Replicate=="B"),
  RunsToCompare,
  'HG03516 B'
)

# Look at with versus without black list for hg38
BL.PreUpset.DF<-spread(unique(subset(All_Original.Filtered, Genome=="hg38.LOCAL" | Genome=="hg38.NoBlackList")[,c(13,14,12,17,15,17)]), Genome, Cluster)

BL.PreUpset.DF<-BL.PreUpset.DF[,-4]

colnames(BL.PreUpset.DF)[colnames(BL.PreUpset.DF)=="hg38.LOCAL"]<-"With blacklist"
colnames(BL.PreUpset.DF)[colnames(BL.PreUpset.DF)=="hg38.NoBlackList"]<-"Without blacklist"

RunsToCompareBL<-colnames(BL.PreUpset.DF)[4:5]

BL.PreUpset.DF[RunsToCompareBL] = !is.na(BL.PreUpset.DF[RunsToCompareBL])
BlackListUpsetPlot<-MakeUpsetPlot(BL.PreUpset.DF,RunsToCompareBL,'Black list inclusion')

### Overall panel
SampleUpsetPanel<-plot_grid(SampleUpsetPlot_HG00621_A,
                            SampleUpsetPlot_HG00621_B,
                            SampleUpsetPlot_HG00741_A,
                            SampleUpsetPlot_HG00741_B,
                            SampleUpsetPlot_HG01952_A,
                            SampleUpsetPlot_HG01952_B,
                            SampleUpsetPlot_HG01978_A,
                            SampleUpsetPlot_HG01978_B,
                            SampleUpsetPlot_HG03516_A,
                            SampleUpsetPlot_HG03516_B,
                            BlackListUpsetPlot,
                            labels = "AUTO",
                            ncol = 4,
                            byrow = TRUE
)

ggsave2(filename = "SampleUpsetPanel_8.png",plot = SampleUpsetPanel, units = "in", height = 9.5, width = 30)
```

```{r plot upset plot HG00621 A, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG00621_A
```

```{r plot upset plot HG00621 B, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG00621_B
```

```{r plot upset plot HG00741 A, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG00741_A
```

```{r plot upset plot HG00741 B, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG00741_B
```

```{r plot upset plot HG01952 A, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG01952_A
```

```{r plot upset plot HG01952 B, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG01952_B
```

```{r plot upset plot HG01978 A, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG01978_A
```

```{r plot upset plot HG01978 B, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG01978_B
```

```{r plot upset plot HG03516 A, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG03516_A
```

```{r plot upset plot HG03516 B, include=TRUE, fig.width=8, fig.height=4}
SampleUpsetPlot_HG03516_B
```

```{r plot upset plot BlackList, include=TRUE, fig.width=4, fig.height=4}
BlackListUpsetPlot
```

```{r save list of peaks in individual assembles which are missing from hg38, include=FALSE}
NonReferenceIndividualAssemblyPeaks<-subset(All_Original, Cluster %in% ClusterNames[(Sample.PreUpset.DF$Maternal | Sample.PreUpset.DF$Paternal) & !Sample.PreUpset.DF$hg38] )
write.table(x = NonReferenceIndividualAssemblyPeaks, file = "NonReferenceIndividualAssemblyPeaks.tsv", quote = FALSE, row.names = FALSE, col.names = TRUE, sep = "\t")
```

```{r how many clusters, include=TRUE}
# How many clusters are there?
length(All_Original$Cluster)
# How many unique clusters are there?
length(unique(All_Original$Cluster))
```

```{r build fraction specific to individual dataframe, include=TRUE}
FractionSpecificToIndividual.DF_8<-rbind(
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & (Maternal==TRUE | Paternal==TRUE) & CHM13==FALSE & hg38==FALSE & pangenome==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & (Maternal==TRUE | Paternal==TRUE) )),
      Sample=SAMPLE,
      Replicate="A",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows(),
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & (Maternal==TRUE | Paternal==TRUE) & CHM13==FALSE & hg38==FALSE & pangenome==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & (Maternal==TRUE | Paternal==TRUE) )),
      Sample=SAMPLE,
      Replicate="B",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows()
)

FractionSpecificToIndividual.DF_8
```

```{r build fraction specific to non-linear reference dataframe, include=TRUE}
FractionSpecificToNonLinear.DF_8<-rbind(
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & CHM13==FALSE & hg38==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A")),
      Sample=SAMPLE,
      Replicate="A",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows(),
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & CHM13==FALSE & hg38==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B")),
      Sample=SAMPLE,
      Replicate="B",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B"))
    )
  ) %>% bind_rows()
)

FractionSpecificToNonLinear.DF_8
```

```{r build fraction specific to pangenome reference dataframe, include=TRUE}
FractionSpecificToPangenome.DF_8<-rbind(
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & CHM13==FALSE & hg38==FALSE & pangenome==TRUE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A")),
      Sample=SAMPLE,
      Replicate="A",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows(),
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & CHM13==FALSE & hg38==FALSE & pangenome==TRUE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B")),
      Sample=SAMPLE,
      Replicate="B",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B"))
    )
  ) %>% bind_rows()
)

FractionSpecificToPangenome.DF_8
```
```{r build fraction specific to chm13 reference dataframe, include=TRUE}
FractionSpecificToCHM13.DF_8<-rbind(
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & CHM13==TRUE & hg38==FALSE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A")),
      Sample=SAMPLE,
      Replicate="A",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows(),
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & CHM13==TRUE & hg38==FALSE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B")),
      Sample=SAMPLE,
      Replicate="B",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B"))
    )
  ) %>% bind_rows()
)

FractionSpecificToCHM13.DF_8
```

```{r build fraction specific to hg38 reference dataframe, include=TRUE}
FractionSpecificToHG38.DF_8<-rbind(
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A" & hg38==TRUE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A")),
      Sample=SAMPLE,
      Replicate="A",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="A"))
    )
  ) %>% bind_rows(),
  lapply(
    unique(Sample.PreUpset.DF$Sample),
    function(SAMPLE) data.frame(
      SpecificFraction=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B" & hg38==TRUE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE))/nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B")),
      Sample=SAMPLE,
      Replicate="B",
      NumberTotal=nrow(subset(Sample.PreUpset.DF, Sample==SAMPLE & Replicate=="B"))
    )
  ) %>% bind_rows()
)

FractionSpecificToHG38.DF_8
```

```{r build reproducibility function, include=FALSE}
makeReproducibilityPlot<-function(SAMPLE,THRESHOLD){
  TESTDF<-spread(unique(subset(All_Original, Sample==SAMPLE & SignalValue>=THRESHOLD & Genome!="hg38.NoBlackList")[,c(13,14,12,15,17,17)]), Replicate, Cluster)
  
  TESTDF<-TESTDF[,-4]
  
  RunsToCompare<-colnames(TESTDF)[4:5]
  
  TESTDF[RunsToCompare] = !is.na(TESTDF[RunsToCompare])
  
  ReproducibilityUpsetPlot.CHM13<-MakeUpsetPlot(subset(TESTDF,Genome=="CHM13"),RunsToCompare,paste("CHM13",SAMPLE,"reproducibilty. SignalThreshold>=",THRESHOLD,sep=" "))
  ReproducibilityUpsetPlot.CHM13
  
  ReproducibilityUpsetPlot.hg38<-MakeUpsetPlot(subset(TESTDF,Genome=="hg38.LOCAL"),RunsToCompare,paste("hg38",SAMPLE,"reproducibilty. SignalThreshold>=",THRESHOLD,sep=" "))
  ReproducibilityUpsetPlot.hg38
  
  ReproducibilityUpsetPlot.Maternal<-MakeUpsetPlot(subset(TESTDF,Genome=="Maternal"),RunsToCompare,paste("Maternal","reproducibilty. SignalThreshold>=",THRESHOLD,sep=" "))
  ReproducibilityUpsetPlot.Maternal
  
  ReproducibilityUpsetPlot.Paternal<-MakeUpsetPlot(subset(TESTDF,Genome=="Paternal"),RunsToCompare,paste("Paternal","reproducibilty. SignalThreshold>=",THRESHOLD,sep=" "))
  ReproducibilityUpsetPlot.Paternal
  
  Reproducibility.SampleUpsetPanel<-plot_grid(
    ReproducibilityUpsetPlot.CHM13,
    ReproducibilityUpsetPlot.hg38,
    ReproducibilityUpsetPlot.Maternal,
    ReproducibilityUpsetPlot.Paternal,
    labels = NULL,
    ncol = 4,
    byrow = TRUE
  )
  
  return(Reproducibility.SampleUpsetPanel)
}
```

```{r generate reproducibility plots, include=FALSE}
# HG01952
ReproducibilityPanel.HG01952<-plot_grid(
  makeReproducibilityPlot("HG01952",1),
  makeReproducibilityPlot("HG01952",2),
  makeReproducibilityPlot("HG01952",4),
  makeReproducibilityPlot("HG01952",8),
  makeReproducibilityPlot("HG01952",16),
  ncol=1,
  labels = "AUTO"
)

ggsave2(filename = "ReproducibilityPanel.HG01952.png", plot = ReproducibilityPanel.HG01952, units = "in", height = 16, width = 18)

# HG01978
ReproducibilityPanel.HG01978<-plot_grid(
  makeReproducibilityPlot("HG01978",1),
  makeReproducibilityPlot("HG01978",2),
  makeReproducibilityPlot("HG01978",4),
  makeReproducibilityPlot("HG01978",8),
  makeReproducibilityPlot("HG01978",16),
  ncol=1,
  labels = "AUTO"
)

ggsave2(filename = "ReproducibilityPanel.HG01978.png", plot = ReproducibilityPanel.HG01978, units = "in", height = 16, width = 18)

# HG03516
ReproducibilityPanel.HG03516<-plot_grid(
  makeReproducibilityPlot("HG03516",1),
  makeReproducibilityPlot("HG03516",2),
  makeReproducibilityPlot("HG03516",4),
  makeReproducibilityPlot("HG03516",8),
  makeReproducibilityPlot("HG03516",16),
  ncol=1,
  labels = "AUTO"
)

ggsave2(filename = "ReproducibilityPanel.HG03516.png", plot = ReproducibilityPanel.HG03516, units = "in", height = 16, width = 18)

# HG00621
ReproducibilityPanel.HG00621<-plot_grid(
  makeReproducibilityPlot("HG00621",1),
  makeReproducibilityPlot("HG00621",2),
  makeReproducibilityPlot("HG00621",4),
  makeReproducibilityPlot("HG00621",8),
  makeReproducibilityPlot("HG00621",16),
  ncol=1,
  labels = "AUTO"
)

ggsave2(filename = "ReproducibilityPanel.HG00621.png", plot = ReproducibilityPanel.HG00621, units = "in", height = 16, width = 18)

# HG00741
ReproducibilityPanel.HG00741<-plot_grid(
  makeReproducibilityPlot("HG00741",1),
  makeReproducibilityPlot("HG00741",2),
  makeReproducibilityPlot("HG00741",4),
  makeReproducibilityPlot("HG00741",8),
  makeReproducibilityPlot("HG00741",16),
  ncol=1,
  labels = "AUTO"
)

ggsave2(filename = "ReproducibilityPanel.HG00741.png", plot = ReproducibilityPanel.HG00741, units = "in", height = 16, width = 18)
```

```{r save list of peaks in specific to pangenome}
PangenomePeaks<-rbind(  
subset(All_Original, Sample=="HG00621" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00621" & Replicate=="A" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG00621" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00621" & Replicate=="B" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG00741" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00741" & Replicate=="A" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG00741" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00741" & Replicate=="B" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG01952" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01952" & Replicate=="A" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG01952" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01952" & Replicate=="B" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG01978" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01978" & Replicate=="A" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG01978" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01978" & Replicate=="B" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG03516" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG03516" & Replicate=="A" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1),
subset(All_Original, Sample=="HG03516" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG03516" & Replicate=="B" & pangenome ==TRUE & hg38==FALSE & CHM13==FALSE & Maternal==FALSE & Paternal==FALSE)$Cluster.1)
)

# Change hg38.LOCAL and hg38.NoBlackList to hg38 and "hg38 nb"
PangenomePeaks$Genome[PangenomePeaks$Genome=="hg38.LOCAL"]<-"hg38"
PangenomePeaks$Genome[PangenomePeaks$Genome=="hg38.NoBlackList"]<-"hg38 nbl"

write.table(x = PangenomePeaks, file = "PangenomeSpecificPeaks.tsv", quote = FALSE, row.names = FALSE, col.names = TRUE, sep = "\t")
```
```{r plot signal value distribution of pangenome specific peak calls, include=TRUE, fig.width=8.5, fig.height=4.5}
PangenomeSpecificPeaks_SignalValueDist<-ggplot(PangenomePeaks, aes(x=Genome, y=SignalValue))+
  geom_violin(bw=0.025)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "red")+
  #geom_jitter(width = 0.25, size=0.05)+
  CS.THEME+
  theme(axis.text.x = element_text(angle = 45, hjust = 1))+
  scale_y_continuous(trans = "log2")+
  facet_grid(Replicate~Sample)
# The points below the threshold for the pangenome given we are looking at pan genome specific peaks are isntances of multiple peaks for a given run within a cluster

# Save
ggsave2(filename = "PangenomeSpecificPeaks_SignalValueDist.png", plot = PangenomeSpecificPeaks_SignalValueDist, units = "in", height = 4.5, width = 8.5)

PangenomeSpecificPeaks_SignalValueDist
```

```{r plot positions of pangenome specific peaks, include=FALSE}
# make Start numeric
PangenomePeaks$Start<-as.numeric(PangenomePeaks$Start)

makeManhattenPlot<-function(dataObj,genomeSizeObj,Chrome,highlightDF=NULL){
  
  if(!is.null(highlightDF)){
  ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_point(size=1.5, alpha=0.75, stroke=0)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "black")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000))+
  facet_grid(Sample~Chromosome)+
  xlab("Postion (Mb)")
  }else{
  ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_point(size=1.5, alpha=0.75, stroke=0)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "black")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000))+
  facet_grid(Sample~Chromosome)+
  xlab("Postion (Mb)")
  }
  
}

PangenomePeaks_plot_list <- list(
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr1")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr2")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr3")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr4")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr5")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr6")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr7")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr8")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr9")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr10")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr11")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr12")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr13")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr14")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr15")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr16")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr17")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr18")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr19")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr20")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr21")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr22")+theme(legend.position = "none")
)
# Make panel
PangenomePeaks_ManhattenPanel<-plot_grid( plotlist = PangenomePeaks_plot_list, ncol = 11, nrow = 2)

# Extract legend
PangenomePeaks_ManhattenPanel.legendplot<-as_ggplot(get_legend(makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr1")+theme(legend.position = "bottom")))

# Add legend to plot
PangenomePeaks_ManhattenPanel.CombinedPlot<-plot_grid(PangenomePeaks_ManhattenPanel, PangenomePeaks_ManhattenPanel.legendplot, ncol=1, rel_heights = c(1, 0.05))

# Clean up
rm(PangenomePeaks_plot_list, PangenomePeaks_ManhattenPanel.legendplot)
```
```{r save and plot manhatten plot of pangenome specific peaks, include=TRUE, fig.width=45, fig.height=24}
ggsave2(filename = "PangenomePeaks_ManhattenPanel.png", plot = PangenomePeaks_ManhattenPanel.CombinedPlot, units = "in", height = 24, width = 45)
PangenomePeaks_ManhattenPanel.CombinedPlot
```

```{r generate cherry picked example chr14, fig.width=5, fig.height=10}
HGSVCdata<-read.delim("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/HGSVC_SV_Enrichment/HGSVC_SV_Hotspots.bed", header = TRUE)

PangenomePeaks_Manhatten_Chr14<-makeManhattenPlot(PangenomePeaks,GenomeSizes[c("Chromsome","hg38")],"chr14",subset(HGSVCdata, Chr=="chr14") )+theme(legend.position = "bottom")
ggsave2(filename = "PangenomePeaks_Manhatten_Chr14.png", plot = PangenomePeaks_Manhatten_Chr14, units = "in", height = 10, width = 5)

PangenomePeaks_Manhatten_Chr14
```


```{r save list of peaks in missing from pangenome}
PangenomeMissingPeaks<-rbind(  
subset(All_Original, Sample=="HG00621" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00621" & Replicate=="A" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG00621" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00621" & Replicate=="B" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG00741" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00741" & Replicate=="A" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG00741" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG00741" & Replicate=="B" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG01952" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01952" & Replicate=="A" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG01952" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01952" & Replicate=="B" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG01978" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01978" & Replicate=="A" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG01978" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG01978" & Replicate=="B" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG03516" & Replicate=="A" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG03516" & Replicate=="A" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1),
subset(All_Original, Sample=="HG03516" & Replicate=="B" & Cluster%in% subset(Sample.PreUpset.DF, Sample=="HG03516" & Replicate=="B" & pangenome ==FALSE & hg38==TRUE & CHM13==TRUE & Maternal==TRUE & Paternal==TRUE)$Cluster.1)
)

# Change hg38.LOCAL and hg38.NoBlackList to hg38 and "hg38 nb"
PangenomeMissingPeaks$Genome[PangenomeMissingPeaks$Genome=="hg38.LOCAL"]<-"hg38"
PangenomeMissingPeaks$Genome[PangenomeMissingPeaks$Genome=="hg38.NoBlackList"]<-"hg38 nbl"

write.table(x = PangenomeMissingPeaks, file = "PangenomeMissingPeaks.tsv", quote = FALSE, row.names = FALSE, col.names = TRUE, sep = "\t")
```
```{r plot signal value distribution of pangenome missing peak calls, include=TRUE, fig.width=8.5, fig.height=4.5}
PangenomeMissingPeaks_SignalValueDist<-ggplot(PangenomeMissingPeaks, aes(x=Genome, y=SignalValue))+
  geom_violin(bw=0.025)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "red")+
  #geom_jitter(width = 0.25, size=0.05)+
  CS.THEME+
  theme(axis.text.x = element_text(angle = 45, hjust = 1))+
  scale_y_continuous(trans = "log2")+
  facet_grid(Replicate~Sample)

# Save
ggsave2(filename = "PangenomeMissingPeaks_SignalValueDist.png", plot = PangenomeMissingPeaks_SignalValueDist, units = "in", height = 4.5, width = 8.5)

PangenomeMissingPeaks_SignalValueDist
```

```{r plot positions of pangenome missing peaks, include=FALSE}
# make Start numeric
PangenomeMissingPeaks$Start<-as.numeric(PangenomeMissingPeaks$Start)

PangenomeMissingPeaks_plot_list <- list(
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr1")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr2")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr3")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr4")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr5")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr6")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr7")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr8")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr9")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr10")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr11")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr12")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr13")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr14")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr15")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr16")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr17")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr18")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr19")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr20")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr21")+theme(legend.position = "none"),
  makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr22")+theme(legend.position = "none")
)

# Make panel
PangenomeMissingPeaks_ManhattenPanel<-plot_grid( plotlist = PangenomeMissingPeaks_plot_list, ncol = 11, nrow = 2)

# Extract legend
PangenomeMissingPeaks_ManhattenPanel.legendplot<-as_ggplot(get_legend(makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr1")+theme(legend.position = "bottom")))

# Add legend to plot
PangenomeMissingPeaks_ManhattenPanel.CombinedPlot<-plot_grid(PangenomeMissingPeaks_ManhattenPanel, PangenomeMissingPeaks_ManhattenPanel.legendplot, ncol=1, rel_heights = c(1, 0.05))

# Clean up
rm(PangenomeMissingPeaks_plot_list, PangenomeMissingPeaks_ManhattenPanel.legendplot)
```
```{r save and plot manhatten plot of pangenome missing peaks, include=TRUE, fig.width=45, fig.height=24}
ggsave2(filename = "PangenomeMissingPeaks_ManhattenPanel.png", plot = PangenomeMissingPeaks_ManhattenPanel.CombinedPlot, units = "in", height = 24, width = 45)
PangenomeMissingPeaks_ManhattenPanel.CombinedPlot
```

```{r generate cherry picked example of pangenome missing chr1, fig.width=5, fig.height=10}
PangenomeMissingPeaks_Manhatten_Chr1<-makeManhattenPlot(PangenomeMissingPeaks,GenomeSizes[c("Chromsome","hg38")],"chr1",subset(HGSVCdata, Chr=="chr1") )+theme(legend.position = "bottom")
ggsave2(filename = "PangenomeMissingPeaks_Manhatten_Chr1.png", plot = PangenomeMissingPeaks_Manhatten_Chr1, units = "in", height = 10, width = 5)

PangenomeMissingPeaks_Manhatten_Chr1
```

```{r load in gzipped bedgraph files}
# for examples of pangenome reads changing fate
# Load in bedgraph files

HG00621_A_Pangenome_hg38_fate_2_query <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_pangenome.hg38_fate_2_query.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_2_query)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_3_query <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_pangenome.hg38_fate_3_query.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_3_query)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_6_query <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_pangenome.hg38_fate_6_query.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_6_query)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_8_query <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_pangenome.hg38_fate_8_query.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_8_query)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_4_reference <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_hg38.LOCAL_fate_4_reference.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_4_reference)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_6_reference <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_hg38.LOCAL_fate_6_reference.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_6_reference)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_7_reference <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_hg38.LOCAL_fate_7_reference.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_7_reference)<-c("Chromosome","Start","End","Coverage")

HG00621_A_Pangenome_hg38_fate_8_reference <- read.table(gzfile("/Users/juanmacias/Library/CloudStorage/Box-Box/LawsonLab/JuanMacias/Postdoc/HPRC/ATACseq/AutomaticTesting/Latest/Pangenome_ReadTrace_fate_BedGraphs/BedGraphs/Renamed_sorted_step2.1_trimed_HG00621_A_hg38.LOCAL_fate_8_reference.bedgraph.gz"), header = FALSE)
colnames(HG00621_A_Pangenome_hg38_fate_8_reference)<-c("Chromosome","Start","End","Coverage")
```

```{r fate change manhatten life function}
makeFateChangeManhattenPlot<-function(dataObj,genomeSizeObj,Chrome,Fate2queryBedgrap,Fate3queryBedgrap,Fate6queryBedgrap,Fate8queryBedgrap,Fate4RefBedgrap,Fate6RefBedgrap,Fate7RefBedgrap,Fate8RefBedgrap,highlightDF=NULL){
  
  if(!is.null(highlightDF)){
  highlightDF<-subset(highlightDF, Chr==Chrome)
  
  Bottom<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_point(size=1.5, alpha=0.75, stroke=0)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "black")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  theme(legend.position = "none")
  
  
  Top<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate2queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  facet_grid(.~Chromosome)+
  xlab("Postion (Mb)")+
  ylab("Fate 2 Query\nCoverage")
  
  Top2<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate3queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 3 Query\nCoverage")

  Top3<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate6queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 6 Query\nCoverage")

  Top4<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate4RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 4 Ref\nCoverage")  

  Top5<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate6RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 6 Ref\nCoverage")    

  Top6<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate7RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 7 Ref\nCoverage")
  
  Top7<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate8RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 8 Ref\nCoverage")
  
  Top8<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_rect(data = highlightDF, inherit.aes = FALSE, aes(xmin = Start/1000000, xmax = End/1000000, ymin = -Inf, ymax = Inf), fill = "#55575725", alpha = 0.6)+
  geom_line(data = subset(Fate6queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 8 Query\nCoverage")
  
  plot_grid(Top, Top2, Top3, Top8, Top4, Top5, Top6, Top7, Bottom, ncol=1, labels = "AUTO")
  
  }else{
  
  
  Bottom<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_point(size=1.5, alpha=0.75, stroke=0)+
  geom_hline(yintercept = 8, linetype = "dashed", color = "black")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  theme(legend.position = "none")
  
  Top<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate2queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  facet_grid(.~Chromosome)+
  xlab("Postion (Mb)")+
  ylab("Fate 2 Query\nCoverage")
  
  Top2<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate3queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 3 Query\nCoverage")

  Top3<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate3queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 6 Query\nCoverage")

  Top4<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate4RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 4 Ref\nCoverage")
  
  Top5<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate6RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 6 Ref\nCoverage")

  Top6<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate7RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 7 Ref\nCoverage")

  Top7<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate8RefBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 8 Ref\nCoverage")

  Top8<-ggplot(subset(dataObj, Chromosome==Chrome), aes(x=Start/1000000,y=SignalValue, color=Genome) )+
  geom_line(data = subset(Fate8queryBedgrap, Chromosome==Chrome), aes(x=Start/1000000, y=Coverage), color = "red")+
  CS.THEME+
  scale_color_viridis(discrete = TRUE, option = "H")+
  scale_x_continuous(limits = c(0,genomeSizeObj[genomeSizeObj$Chromsome==Chrome,2]/1000000), n.breaks = 15)+
  xlab("Postion (Mb)")+
  ylab("Fate 8 Query\nCoverage")
  
  plot_grid(Top, Top2, Top3, Top8, Top4, Top5, Top6, Top7, Bottom, ncol=1, labels = "AUTO")
  
  }
  
}

```


```{r plot Chromosome 1 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make Start numeric
PangenomePeaks$Start<-as.numeric(PangenomePeaks$Start)

# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_1_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr1",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_1_plot
```

```{r plot Chromosome 2 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_2_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr2",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_2_plot
```

```{r plot Chromosome 3 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_3_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr3",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_3_plot
```

```{r plot Chromosome 4 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_4_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr4",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_4_plot
```

```{r plot Chromosome 5 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_5_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr5",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_5_plot
```

```{r plot Chromosome 6 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_6_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr6",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_6_plot
```

```{r plot Chromosome 7 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_7_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr7",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_7_plot
```

```{r plot Chromosome 8 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_8_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr8",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_8_plot
```

```{r plot Chromosome 9 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_9_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr9",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_9_plot
```

```{r plot Chromosome 10 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_10_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr10",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_10_plot
```

```{r plot Chromosome 11 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_11_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr11",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_11_plot
```

```{r plot Chromosome 12 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_12_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr12",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_12_plot
```

```{r plot Chromosome 13 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_13_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr13",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_13_plot
```

```{r plot Chromosome 14 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_14_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr14",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_14_plot
```

```{r plot Chromosome 15 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_15_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr15",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_15_plot
```

```{r plot Chromosome 16 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_16_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr16",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_16_plot
```

```{r plot Chromosome 17 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_17_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr17",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_17_plot
```

```{r plot Chromosome 18 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_18_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr18",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_18_plot
```

```{r plot Chromosome 19 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_19_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr19",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_19_plot
```

```{r plot Chromosome 20 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_20_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr20",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_20_plot
```

```{r plot Chromosome 21 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_21_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr21",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_21_plot
```

```{r plot Chromosome 22 HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_22_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chr22",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_22_plot
```

```{r plot Chromosome X HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_X_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chrX",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_X_plot
```

```{r plot Chromosome Y HG00621 pangenome specific peak locations compared to shifted fate coverage, include=TRUE, fig.height=25, fig.width=10}
# Make plot
HG00621_A_Pangenome_hg38_fate_specificity__chromosome_Y_plot<-makeFateChangeManhattenPlot(
  subset(PangenomePeaks, Sample=="HG00621" & Replicate=="A"),
  GenomeSizes[c("Chromsome","hg38")],
  "chrY",
  HG00621_A_Pangenome_hg38_fate_2_query,
  HG00621_A_Pangenome_hg38_fate_3_query,
  HG00621_A_Pangenome_hg38_fate_6_query,
  HG00621_A_Pangenome_hg38_fate_8_query,
  HG00621_A_Pangenome_hg38_fate_4_reference,
  HG00621_A_Pangenome_hg38_fate_6_reference,
  HG00621_A_Pangenome_hg38_fate_7_reference,
  HG00621_A_Pangenome_hg38_fate_8_reference,
  HGSVCdata
  )

HG00621_A_Pangenome_hg38_fate_specificity__chromosome_Y_plot
```

```{r prepare for accessability PCA, include=FALSE}
# Generate list of peaks shared by all genomes
ClusterNames.SharedAll<-ClusterNames[rowSums(Sample.PreUpset.DF[,5:9])==4]

# Filter for shared peaks
All_Original.Filtered.SharedAll<-subset(All_Original, Cluster %in% ClusterNames.SharedAll)

# Remove unneeded columns
All_Original.Filtered.SharedAll.PCA<-All_Original.Filtered.SharedAll[,c(13,14,15,7,17,11)]

# Mark peaks with multiple peaks in cluster from the same run
All_Original.Filtered.SharedAll.PCA$Duplicated<-duplicated(paste(All_Original.Filtered.SharedAll.PCA$Cluster,All_Original.Filtered.SharedAll.PCA$Run,sep="_"))

All_Original.Filtered.SharedAll.PCA$Duplicated

# I only included peaks which are not duplicated. I believe these duplication occur when in one run two peaks are called where in another run it's one large peak.
# Remove duplicated peaks and spread to wide format
All_Original.Filtered.SharedAll.PCA.Wide<-spread(subset(All_Original.Filtered.SharedAll.PCA,Duplicated==FALSE)[,c(4,5,6)], Cluster, SignalValue)

# How many peaks remain?
print(ncol(All_Original.Filtered.SharedAll.PCA.Wide))

# Check clusters for NAs
TestsForNAinPCAWide<-colSums(apply( All_Original.Filtered.SharedAll.PCA.Wide[,2:ncol(All_Original.Filtered.SharedAll.PCA.Wide)], MARGIN = 2, is.na ))==0

# Extract names of clusters without NAs
NamesofClustersWithoutNAs<-colnames(All_Original.Filtered.SharedAll.PCA.Wide[,2:ncol(All_Original.Filtered.SharedAll.PCA.Wide)][,TestsForNAinPCAWide])

# Remove clusters with NAs
All_Original.Filtered.SharedAll.PCA.Wide.NAremoved<-All_Original.Filtered.SharedAll.PCA.Wide[,colnames(All_Original.Filtered.SharedAll.PCA.Wide) %in% c("Run",NamesofClustersWithoutNAs)]
```

```{r perform PCA}
library(factoextra)
# Perform PCA
res.pca<-prcomp(All_Original.Filtered.SharedAll.PCA.Wide.NAremoved[,2:ncol(All_Original.Filtered.SharedAll.PCA.Wide.NAremoved)], scale=TRUE)

# Extract group information for plotting and partial eta squared estimation
groups.Sample <- as.factor( unlist(lapply(All_Original.Filtered.SharedAll.PCA.Wide.NAremoved[,1], function(X) strsplit(X,split = "_")[[1]][1])) )
groups.Replicate <- as.factor(unlist(lapply(All_Original.Filtered.SharedAll.PCA.Wide.NAremoved[,1], function(X) strsplit(X,split = "_")[[1]][2])))
groups.Genome <- unlist(lapply(All_Original.Filtered.SharedAll.PCA.Wide.NAremoved[,1], function(X) strsplit(X,split = "_")[[1]][3]))
groups.Genome[groups.Genome %in% c("HG00621.maternal","HG00741.maternal","HG01952.maternal","HG01978.maternal","HG03516.maternal")]<-"Maternal"
groups.Genome[groups.Genome %in% c("HG00621.paternal.wMito","HG00741.paternal.wMito","HG01952.paternal.wMito","HG01978.paternal.wMito","HG03516.paternal.wMito")]<-"Paternal"
groups.Genome[groups.Genome=="hg38.LOCAL"]<-"hg38"
groups.Genome[groups.Genome=="hg38.NoBlackList"]<-"hg38 nb"
groups.Genome[groups.Genome=="pangenome.hg38"]<-"pangenome"
groups.Genome<-as.factor(groups.Genome)
```

```{r perform partial eta square estimation, include=TRUE}
# Generate variance partitioning object
PCA.VarObject<-cbind(res.pca$x,data.frame(Sample=groups.Sample),data.frame(Replicate=groups.Replicate),data.frame(Genome=groups.Genome))

# Perform MANOVA
manova_model<-manova(cbind(PC1,PC2,PC3,PC4,PC5,PC6,PC7,PC8,PC9,PC10,PC11,PC12)~Sample*Genome+Replicate,PCA.VarObject)
manova_model.Summary<-summary(manova_model)
aov_results <- summary.aov(manova_model)

# print the MANOVA results
aov_results

# Define the number of PCs consider for partial eta squared estimation
NUM.PCs<-12

# Estimate partial eta squareds
PC.PartialEtaSquareds<-lapply(1:NUM.PCs,
                              function(PC){aov_results[[PC]][[2]][1:5]/sum(aov_results[[PC]][[2]])}
) %>% do.call(rbind,.) %>% as.data.frame 
colnames(PC.PartialEtaSquareds)<-c("Sample","Genome","Sample:Genome","Replicate","Residual")

# Extract statistics
PC.Statistics<-cbind(as.factor(1:NUM.PCs),get_eig(res.pca)[1:NUM.PCs,],PC.PartialEtaSquareds)
colnames(PC.Statistics)<-c("PC","Eigenvalue","VariancePercent","CumulativeVariancePercent","PartialEtaSquared.Sample","PartialEtaSquared.Genome","PartialEtaSquared.Sample:Genome","PartialEtaSquared.Replicate","PartialEtaSquared.Residual")
rownames(PC.Statistics)<-NULL

# Calculate %variance accounted for by each factor
PC.Statistics$VariancePercent.Sample<-PC.Statistics$VariancePercent*PC.Statistics$PartialEtaSquared.Sample
PC.Statistics$VariancePercent.Genome<-PC.Statistics$VariancePercent*PC.Statistics$PartialEtaSquared.Genome
PC.Statistics$VariancePercent.Sample.Genome<-PC.Statistics$VariancePercent*PC.Statistics$`PartialEtaSquared.Sample:Genome`
PC.Statistics$VariancePercent.Replicate<-PC.Statistics$VariancePercent*PC.Statistics$PartialEtaSquared.Replicate
PC.Statistics$VariancePercent.Residual<-PC.Statistics$VariancePercent*PC.Statistics$PartialEtaSquared.Residual

# Save the PC statistics
write.table(PC.Statistics, file = "PC.Statistics.txt", sep = "\t", row.names = FALSE, quote = FALSE)

# Make long df to plot variance percents
PC.Statistics.VariancePercent.Long<-gather(PC.Statistics[,c(1,10:14)],key="VarianceType",value="VariancePercent",VariancePercent.Sample:VariancePercent.Residual)
# clean up names
PC.Statistics.VariancePercent.Long$VarianceType<-gsub("VariancePercent.","",PC.Statistics.VariancePercent.Long$VarianceType)
PC.Statistics.VariancePercent.Long$VarianceType<-gsub("Sample.Genome","Sample:Genome",PC.Statistics.VariancePercent.Long$VarianceType)

# Order factor levels
PC.Statistics.VariancePercent.Long$VarianceType<-factor(PC.Statistics.VariancePercent.Long$VarianceType, levels = c("Sample","Genome","Sample:Genome","Replicate","Residual"), ordered = TRUE)
```

```{r plot variance partitioning, include=TRUE, fig.width=9, fig.height=6}
# Generate plot
Plot.PCs<-ggplot(PC.Statistics.VariancePercent.Long, aes(fill=VarianceType, y=VariancePercent, x=PC)) + 
  geom_bar(position="stack", stat="identity")+
  scale_fill_manual(values = c("#ff7f5d","#2d5879","#b2823f","#aaaaaa","#333434"))+
  #scale_fill_manual(values = c("#2d5879","#aaaaaa","#333434","#ff7f5d","#b2823f"))+
  ylab("Percent of variance")+
  xlab("Principal component")+
  ggtitle("ATACseq - Acessibility\n%Variance captured by PCs partitioned by factor")+
  CS.THEME+
  theme(legend.position="bottom")+
  scale_y_continuous(limits = c(0,round(max(PC.Statistics$VariancePercent)*1.05)), expand = c(0,0))+
  theme(legend.key.size = unit(0.2, "cm"))

# Save
ggsave2(filename = "Peaks_PCs.png",plot = Plot.PCs,units = "in",width = 9, height = 6)

# Print
Plot.PCs
```

```{r generate plot accessability PCA, include=FALSE}
# Color coded by Sample
PCA.Plot.Sample<-fviz_pca_ind(res.pca,
                              col.ind = groups.Sample,
                              palette = viridis(5, end=0.9),
                              repel = TRUE,
                              addEllipses = TRUE,
                              ellipse.type = "convex",
                              title="Accessibility - Sample"
)+
  CS.THEME

# Color coded by Genome
PCA.Plot.Genome<-fviz_pca_ind(res.pca,
                              col.ind = groups.Genome,
                              palette = viridis(6,option = "magma", end = 0.8),
                              repel = TRUE,
                              title="Accessibility - Genome"
)+
  CS.THEME

# Color coded by Replicate
PCA.Plot.Replicate<-fviz_pca_ind(res.pca,
                                 col.ind = groups.Replicate,
                                 palette = viridis(2,option = "cividis", end = 0.8),
                                 repel = TRUE,
                                 title="Accessibility - Replicate"
)+
  CS.THEME

# Combine plots
PCA.Panel<-plot_grid(PCA.Plot.Sample,PCA.Plot.Genome,PCA.Plot.Replicate,labels = c("A","B","C"),ncol=3)

# Save plot
ggsave2(filename = "All.Shared.Peaks.PCA.Panel.png",plot = PCA.Panel, units = "in", width = 17*1, height = 6*0.75)
```

```{r plot accessability PCA, include=TRUE, fig.width=17, fig.height=4.5}
PCA.Panel
```