Last updated: 2019-04-24

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File Version Author Date Message
Rmd 4febc15 brimittleman 2019-04-24 return to original SAF
html 627fc45 brimittleman 2019-04-24 Build site.
html dd07ef7 brimittleman 2019-04-24 Build site.
Rmd 6dc25d8 brimittleman 2019-04-24 update after SAF bug
html 26058a5 brimittleman 2019-04-24 Build site.
Rmd 76900e4 brimittleman 2019-04-24 add plots after parsing for 1 site per
html 12d1cb0 brimittleman 2019-04-23 Build site.
Rmd e985ecd brimittleman 2019-04-23 add initial plot
html 214c05c brimittleman 2019-04-23 Build site.
Rmd 27b11e3 brimittleman 2019-04-23 start signal site analysis

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
library(reshape2)

Attaching package: 'reshape2'
The following object is masked from 'package:tidyr':

    smiths

In this analysis I will plot the distribution of signal sites upstream of the PAS I have found.

First I use a python script to make a bed file with the 100 base pairs upsream of the PAS:

module load Anaconda3
source activate three-prime-env
mkdir ../data/SignalSiteFiles
python Upstream100Bases_general.py ../data/PAS/APAPAS_GeneLocAnno.5perc.bed ../data/SignalSiteFiles/APAPAS_100up.bed

Now I use bedtools nuc to get the sequence for each of these regions:

sbatch getSeq100up.sh 

I can now run the DistPAS2Sig.py which will give me the location for the signal site for each PAS.I am running this with the 12 most common PAS signal sites.

sbatch run_distPAS2Sig.sh

Upload all of the results:

Loc_AATAAA= read.table("../data/SignalSiteFiles/Loc_AATAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AATAAA")
Loc_AAAAAG= read.table("../data/SignalSiteFiles/Loc_AAAAAG_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AAAAAG")
Loc_AATACA= read.table("../data/SignalSiteFiles/Loc_AATACA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AATACA")
Loc_AATAGA= read.table("../data/SignalSiteFiles/Loc_AATAGA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AATAGA")
Loc_AATATA= read.table("../data/SignalSiteFiles/Loc_AATATA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AATATA")
Loc_ACTAAA= read.table("../data/SignalSiteFiles/Loc_ACTAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="ACTAAA")
Loc_AGTAAA= read.table("../data/SignalSiteFiles/Loc_AGTAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AGTAAA")
Loc_ATTAAA= read.table("../data/SignalSiteFiles/Loc_ATTAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="ATTAAA")
Loc_CATAAA= read.table("../data/SignalSiteFiles/Loc_CATAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="CATAAA")
Loc_GATAAA= read.table("../data/SignalSiteFiles/Loc_GATAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="GATAAA")
Loc_TATAAA= read.table("../data/SignalSiteFiles/Loc_TATAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="TATAAA")
Loc_AAAAAA= read.table("../data/SignalSiteFiles/Loc_AAAAAA_Distance2end.txt", header=F, col.names =c( "PAS", "Distance2PAS")) %>% mutate(Site="AAAAAA")

Join these together:

AllsiteDF=as.data.frame(rbind(Loc_AATAAA,Loc_AAAAAG,Loc_AATACA,Loc_AATAGA,Loc_AATATA,Loc_ACTAAA,Loc_AGTAAA,Loc_ATTAAA, Loc_GATAAA,Loc_TATAAA,Loc_CATAAA, Loc_AAAAAA))
AllsiteDF_sep = AllsiteDF %>% separate(PAS, int=c("GenePeak", "Location"), sep="_")
ggplot(AllsiteDF_sep, aes(x=Distance2PAS, by=Site, col=Site)) + stat_ecdf() + facet_wrap(~Location)

Version Author Date
dd07ef7 brimittleman 2019-04-24
12d1cb0 brimittleman 2019-04-23

Check to see if any PAS have more than one signal site detected:

AllsiteDFmultsites=AllsiteDF %>% group_by(PAS) %>% mutate(nSites=n()) %>% filter(nSites>1)

First take the perfect match within 50 bp then use the closest.

Write out the AllSite in order to use it in the chooseSignalSite.py script:

write.table(AllsiteDF, file="../data/SignalSiteFiles/AllSignalSite.txt", quote=F, col.names = F, row.names = F, sep="\t")
python chooseSignalSite.py ../data/SignalSiteFiles/AllSignalSite.txt ../data/SignalSiteFiles/AllSignalSite_1perPAS.txt
AllsiteDF_1per=read.table(file="../data/SignalSiteFiles/AllSignalSite_1perPAS.txt", col.names = colnames(AllsiteDF)) %>% mutate(NegCount=-1*as.integer(as.character(Distance2PAS)))

Plot

dist2signalsiteplot=ggplot(AllsiteDF_1per, aes(group=Site, x=NegCount, fill=Site)) + geom_histogram(position="stack",bins=50 ) + labs(x="Distance from PAS", y="N annotated Sites", title="Location of annotated signal sites")
dist2signalsiteplot

Version Author Date
dd07ef7 brimittleman 2019-04-24
ggsave(dist2signalsiteplot, file="../output/SignalSitePlot.png")
Saving 7 x 5 in image

Seperate by location:

AllsiteDF_1per_sep= AllsiteDF_1per %>%separate(PAS, int=c("GenePeak", "Location"), sep="_")
dist2signalsiteplot_byloc=ggplot(AllsiteDF_1per_sep, aes(group=Site, x=NegCount, fill=Site)) + geom_histogram(position="stack",bins=50 ) + labs(x="Distance from PAS", y="N annotated Sites", title="Location of annotated signal sites") + facet_wrap(~Location)

dist2signalsiteplot_byloc

Version Author Date
dd07ef7 brimittleman 2019-04-24
ggsave(dist2signalsiteplot_byloc, file="../output/SignalSitePlotbyLoc.png")
Saving 7 x 5 in image

.

Signal site and usage relationship

Next plot: look at presence of signal site compared to PAS usage

I need to look at the mean usage and fraction it by if the peak has a signal site.


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] reshape2_1.4.3  workflowr_1.3.0 forcats_0.3.0   stringr_1.3.1  
 [5] dplyr_0.8.0.1   purrr_0.3.2     readr_1.3.1     tidyr_0.8.3    
 [9] tibble_2.1.1    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   modelr_0.1.2     magrittr_1.5    
[37] whisker_0.3-2    backports_1.1.2  scales_1.0.0     htmltools_0.3.6 
[41] rvest_0.3.2      assertthat_0.2.0 colorspace_1.3-2 labeling_0.3    
[45] stringi_1.2.4    lazyeval_0.2.1   munsell_0.5.0    broom_0.5.1     
[49] crayon_1.3.4