Last updated: 2019-05-01
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 3153f49 | brimittleman | 2019-05-01 | old hists |
html | 15e195f | brimittleman | 2019-05-01 | Build site. |
Rmd | f5e6fd6 | brimittleman | 2019-05-01 | add random 15 ind hists |
html | 9ccb06e | brimittleman | 2019-04-30 | Build site. |
Rmd | eb0bd95 | brimittleman | 2019-04-30 | add write out step |
html | ac656aa | brimittleman | 2019-04-30 | Build site. |
Rmd | f9b8195 | brimittleman | 2019-04-30 | understand usage of new pas |
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────── tidyverse 1.2.1 ──
✔ ggplot2 3.1.0 ✔ purrr 0.3.2
✔ tibble 2.1.1 ✔ dplyr 0.8.0.1
✔ tidyr 0.8.3 ✔ stringr 1.3.1
✔ readr 1.3.1 ✔ forcats 0.3.0
── Conflicts ───────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag() masks stats::lag()
library(workflowr)
This is workflowr version 1.3.0
Run ?workflowr for help getting started
These results have 30k more PAS than the previous runs. I also see a confusing shift in mean usage for all of the PAS. I want to compare the distribution of usage for different sets of individuals to see if there is something inherently different about the 15 new individuals.
I want to compare the usage of the new peaks compared to the overall mean usage. To do this I need to seperate the new and old PAS.
newPAS5perc=read.table("../data/PAS/APAPAS_GeneLocAnno.5perc.bed", stringsAsFactors = F, col.names = c("chr", "start","end", "ID", "score", "strand"))
oldPAS5perc=read.table("../../threeprimeseq/data/peaks4DT/APAPAS_5percCov_fixedStrand.bed", stringsAsFactors = F, col.names = c("chr", "start", "end", "ID", "score", "strand"))
uniqnew=newPAS5perc %>% semi_join(oldPAS5perc, by=c("chr", "start", "end"))
Pull in the usage of the peaks:
totalPeakUs=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Total.fc", header = T, stringsAsFactors = F) %>% separate(chrom, sep = ":", into = c("chr", "start", "end", "id")) %>% separate(id, sep="_", into=c("gene", "loc", "strand", "peak"))
Warning: Expected 4 pieces. Additional pieces discarded in 4 rows [14735,
14736, 14737, 14738].
ind=colnames(totalPeakUs)[8:dim(totalPeakUs)[2]]
totalPeakUs_CountNum=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Total.CountsOnlyNumeric", col.names = ind)
#numeric with anno
totalPeak=as.data.frame(cbind(totalPeakUs[,1:7], totalPeakUs_CountNum))
totalPeakUs_CountNum_mean=rowMeans(totalPeakUs_CountNum)
#append mean to anno
TotalPeakUSMean=as.data.frame(cbind(totalPeakUs[,1:7],mean=totalPeakUs_CountNum_mean))
uniqnewPasnum=uniqnew %>% separate(ID ,into=c("peaknum", "geneloc"),sep=":") %>% mutate(peak=paste("peak", peaknum, sep="")) %>% select(peak)
Filter these inthe mean usage:
TotalPeakUSMeanClass= TotalPeakUSMean %>% mutate(New=ifelse(peak %in% uniqnewPasnum$peak,"new", "original")) %>% mutate(Cutoff=ifelse(mean>=.05, "Yes", "No"))
mean(TotalPeakUSMean$mean)
[1] 0.2378282
Plot:
ggplot(TotalPeakUSMeanClass, aes(y=mean,x=New)) + geom_violin() + geom_hline(yintercept = mean(TotalPeakUSMean$mean), col="red") + facet_grid(~Cutoff)
Version | Author | Date |
---|---|---|
ac656aa | brimittleman | 2019-04-30 |
This shows me the new peaks are not the peaks that barely passed the cuttoff before. These peaks cover the distribution of usage.
write out file with information about new and old peaks
Peak_newOld=TotalPeakUSMeanClass %>% select(-mean)
write.table(Peak_newOld, file="../data/peaks_5perc/NewVOldPeaks.txt", col.names = T, row.names = F, quote=F)
I want to see if the new 15 individuals are driving the change in the peak mean distribution. I want to make a function that take a vector of individuals, filters the usage dataframe and plots the histogram.
First I will upload the usage dataframe.
totCounts=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Total.fc", stringsAsFactors = F, header = T)
ind=colnames(totCounts)[2:55]
totUsage=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Total.CountsOnlyNumeric", stringsAsFactors = F, header = F,col.names = ind)
batch1.2.3=read.table("../data/MetaDataSequencing.txt", header=T,stringsAsFactors = F)%>% filter(fraction=="total") %>% select(line, batch) %>% filter(batch != 4)
oldind=batch1.2.3$line
batch4=read.table("../data/MetaDataSequencing.txt", header=T,stringsAsFactors = F)%>% filter(fraction=="total") %>% select(line, batch) %>% filter(batch == 4)
newInd=batch4$line
UsageHist= function(indVec,title,totUsage=totUsage){
totUsage_ind=totUsage %>% select(indVec)
meanVec=rowMeans(totUsage_ind)
hist(meanVec, main=title,xlab="Mean Usage")
}
RUn this for different itterations of individuals:
Pick 15 random individuals from old:
sampl1=sample(oldind, 15)
sampl2=sample(oldind, 15)
sampl3=sample(oldind, 15)
sampl4=sample(oldind, 15)
par(mfrow=c(3,2))
UsageHist(indVec=newInd,title="Total Usage New",totUsage=totUsage)
UsageHist(indVec=oldind,title="Total Usage Old",totUsage=totUsage)
UsageHist(indVec=sampl1,title="Total Usage Sample 15 Old",totUsage=totUsage)
UsageHist(indVec=sampl2,title="Total Usage Sample 15 Old",totUsage=totUsage)
UsageHist(indVec=sampl3,title="Total Usage Sample 15 Old",totUsage=totUsage)
UsageHist(indVec=sampl4,title="Total Usage Sample 15 Old",totUsage=totUsage)
Version | Author | Date |
---|---|---|
15e195f | brimittleman | 2019-05-01 |
nucCounts=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Nuclear.fc", stringsAsFactors = F, header = T)
ind=colnames(nucCounts)[2:55]
nucUsage=read.table("../data/phenotype/APApeak_Phenotype_GeneLocAnno.Nuclear.CountsOnlyNumeric", stringsAsFactors = F, header = F,col.names = ind)
UsageHist_nuc= function(indVec,title,nucUsage=nucUsage){
nucUsage_ind=nucUsage %>% select(indVec)
meanVec=rowMeans(nucUsage_ind)
hist(meanVec, main=title,xlab="Mean Usage")
}
par(mfrow=c(3,2))
UsageHist_nuc(indVec=newInd,title="Nuclear Usage New",nucUsage=nucUsage)
UsageHist_nuc(indVec=oldind,title="Nuclear Usage Old",nucUsage=nucUsage)
UsageHist_nuc(indVec=sampl1,title="Nuclear Usage Sample 15 Old",nucUsage=nucUsage)
UsageHist_nuc(indVec=sampl2,title="Nuclear Usage Sample 15 Old",nucUsage=nucUsage)
UsageHist_nuc(indVec=sampl3,title="Nuclear Usage Sample 15 Old",nucUsage=nucUsage)
UsageHist_nuc(indVec=sampl4,title="Nuclear Usage Sample 15 Old",nucUsage=nucUsage)
Old
oldtotalCount=read.table("../../threeprimeseq/data/phenotypes_filtPeakTranscript_noMP_GeneLocAnno/filtered_APApeaks_merged_allchrom_refseqGenes.GeneLocAnno_NoMP_sm_quant.Total.fixed.pheno.fc",header=T,stringsAsFactors = F)
indOld=colnames(oldtotalCount)[2:56]
oldtotalUsage=read.table("../../threeprimeseq/data/phenotypes_filtPeakTranscript_noMP_GeneLocAnno/filtered_APApeaks_merged_allchrom_refseqGenes.GeneLocAnno_NoMP_sm_quant.Total.fixed.pheno.CountsOnlyNumeric.txt",col.names = indOld,stringsAsFactors = F)
par(mfrow=c(3,2))
UsageHist(indVec=newInd,title="Old total Usage",totUsage=oldtotalUsage)
UsageHist(indVec=oldind,title="Old total Usage (39ind)",totUsage=oldtotalUsage)
UsageHist(indVec=sampl1,title="Old total Usage sample 15 ind",totUsage=oldtotalUsage)
UsageHist(indVec=sampl2,title="Old total Usage sample 15 ind",totUsage=oldtotalUsage)
UsageHist(indVec=sampl3,title="Old total Usage sample 15 ind",totUsage=oldtotalUsage)
UsageHist(indVec=sampl4,title="Old total Usage sample 15 ind",totUsage=oldtotalUsage)
Version | Author | Date |
---|---|---|
15e195f | brimittleman | 2019-05-01 |
oldnuclearCount=read.table("../../threeprimeseq/data/phenotypes_filtPeakTranscript_noMP_GeneLocAnno/filtered_APApeaks_merged_allchrom_refseqGenes.GeneLocAnno_NoMP_sm_quant.Nuclear.fixed.pheno.fc",header=T,stringsAsFactors = F)
indOldN=colnames(oldnuclearCount)[2:56]
oldnuclearUsage=read.table("../../threeprimeseq/data/phenotypes_filtPeakTranscript_noMP_GeneLocAnno/filtered_APApeaks_merged_allchrom_refseqGenes.GeneLocAnno_NoMP_sm_quant.Nuclear.fixed.pheno.CountsOnlyNumeric.txt",col.names = indOldN,stringsAsFactors = F)
par(mfrow=c(3,2))
UsageHist_nuc(indVec=newInd,title="Old nuclear Usage",nucUsage=oldnuclearUsage)
UsageHist_nuc(indVec=oldind,title="Old nuclear Usage (39ind)",nucUsage=oldnuclearUsage)
UsageHist_nuc(indVec=sampl1,title="Old nuclear Usage sample 15 ind",nucUsage=oldnuclearUsage)
UsageHist_nuc(indVec=sampl2,title="Old nuclear Usage sample 15 ind",nucUsage=oldnuclearUsage)
UsageHist_nuc(indVec=sampl3,title="Old nuclear Usage sample 15 ind",nucUsage=oldnuclearUsage)
UsageHist_nuc(indVec=sampl4,title="Old nuclear Usage sample 15 ind",nucUsage=oldnuclearUsage)
sessionInfo()
R version 3.5.1 (2018-07-02)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Scientific Linux 7.4 (Nitrogen)
Matrix products: default
BLAS/LAPACK: /software/openblas-0.2.19-el7-x86_64/lib/libopenblas_haswellp-r0.2.19.so
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] workflowr_1.3.0 forcats_0.3.0 stringr_1.3.1 dplyr_0.8.0.1
[5] purrr_0.3.2 readr_1.3.1 tidyr_0.8.3 tibble_2.1.1
[9] ggplot2_3.1.0 tidyverse_1.2.1
loaded via a namespace (and not attached):
[1] Rcpp_1.0.0 cellranger_1.1.0 pillar_1.3.1 compiler_3.5.1
[5] git2r_0.23.0 plyr_1.8.4 tools_3.5.1 digest_0.6.18
[9] lubridate_1.7.4 jsonlite_1.6 evaluate_0.12 nlme_3.1-137
[13] gtable_0.2.0 lattice_0.20-38 pkgconfig_2.0.2 rlang_0.3.1
[17] cli_1.0.1 rstudioapi_0.10 yaml_2.2.0 haven_1.1.2
[21] withr_2.1.2 xml2_1.2.0 httr_1.3.1 knitr_1.20
[25] hms_0.4.2 generics_0.0.2 fs_1.2.6 rprojroot_1.3-2
[29] grid_3.5.1 tidyselect_0.2.5 glue_1.3.0 R6_2.3.0
[33] readxl_1.1.0 rmarkdown_1.10 reshape2_1.4.3 modelr_0.1.2
[37] magrittr_1.5 whisker_0.3-2 backports_1.1.2 scales_1.0.0
[41] htmltools_0.3.6 rvest_0.3.2 assertthat_0.2.0 colorspace_1.3-2
[45] labeling_0.3 stringi_1.2.4 lazyeval_0.2.1 munsell_0.5.0
[49] broom_0.5.1 crayon_1.3.4