Last updated: 2020-03-23

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Knit directory: apaQTL/analysis/

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Unstaged changes:
    Modified:   analysis/NuclearSpecIncludeNotTested.Rmd
    Modified:   analysis/PASdescriptiveplots.Rmd
    Modified:   analysis/Readdistagainstfeatures.Rmd
    Modified:   analysis/TSS.Rmd
    Modified:   analysis/apabyeQTLstatus.Rmd
    Modified:   analysis/decayAndStability.Rmd
    Modified:   analysis/miRNAdisrupt.Rmd
    Modified:   analysis/nascenttranscription.Rmd
    Modified:   analysis/nucSpecinEQTLs.Rmd
    Modified:   analysis/overlapapaqtlsandeqtls.Rmd
    Modified:   analysis/pQTLexampleplot.Rmd
    Modified:   analysis/splicesitestrength.Rmd
    Modified:   analysis/version15bpfilter.Rmd
    Modified:   code/DistPAS2Sig.py
    Modified:   code/Script4NuclearQTLexamples.sh
    Modified:   code/Script4TotalQTLexamples.sh
    Modified:   code/apaQTLsnake.err
    Modified:   code/apaqtlfacetboxplots.R
    Modified:   code/environment.yaml
    Modified:   code/run_qtlFacetBoxplots.sh
    Deleted:    code/test.txt
    Deleted:    reads_graphs.Rmd

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File Version Author Date Message
Rmd 864dacc brimittleman 2020-03-23 change labels for supp
html 6cfa831 brimittleman 2019-09-11 Build site.
Rmd 74a6602 brimittleman 2019-09-11 add number or reads
html 3b25860 brimittleman 2019-09-04 Build site.
html 191d71f brimittleman 2019-08-07 Build site.
Rmd 01d0be5 brimittleman 2019-08-07 add reads_graph analysis

I first install and download all necessary libraries and packages

Then, I am reading in my file, and then only keeping the columns that I need: mapped, mapped no mispriming, reads, and the Sample Line ID.

df <- read.delim("../data/MetaDataSequencing.txt")
keeps <- c("line","fraction", "reads", "mapped", "Mapped_noMP")
frac_dif <- df[keeps]

Next, I am dividing the data set into it’s two categories: nuclear and total

nuclear <- subset(frac_dif, fraction == "nuclear", c(fraction, line, reads, mapped, Mapped_noMP))
total <- subset(frac_dif, fraction == "total", c(fraction, line, reads, mapped, Mapped_noMP))

Here, I create my data matrices. Each are proportions of reads. There is mapped, mapped with mispriming, mapped without mispriming, and unmapped. I do this for both nuclear and total.

#nuclear proportions
nuc_mapped_prop <- data.matrix(nuclear$mapped/nuclear$reads)
nuc_mapped_noMP_prop <- data.matrix(nuclear$Mapped_noMP/nuclear$reads)
nuc_mapped_MP <- nuc_mapped_prop - nuc_mapped_noMP_prop
nuc_none <- 1 - nuc_mapped_prop
nuc_lines <- data.matrix(nuclear$line)

#total proportions
total_mapped_prop <- data.matrix(total$mapped/total$reads)
total_mapped_noMP_prop <- data.matrix(total$Mapped_noMP/total$reads)
total_mapped_MP <-total_mapped_prop - total_mapped_noMP_prop
total_none <- 1 - total_mapped_prop
total_lines <- data.matrix(total$line)

Then, I combine these proportions into a large data frame called “combination”, which I can then easily create my plots.The gather() function tidies my data so that it is in the format that ggplot uses to create the bar plots. I then make the type column a factor with 3 levels. These levels allow me to order the stacks in the way I want them to.

nuc_combination <- data.frame(nuc_lines, nuc_mapped_noMP_prop, nuc_mapped_MP, nuc_none)
nuc_combination <- gather(nuc_combination, nuc_mapped_noMP_prop, nuc_mapped_MP, nuc_none, key = "type", value = "count")
nuc_combination$type <- factor(nuc_combination$type, levels=c("nuc_none", "nuc_mapped_MP", "nuc_mapped_noMP_prop"))

total_combination <- data.frame(total_lines, total_mapped_noMP_prop, total_mapped_MP, total_none)
total_combination <- gather(total_combination, total_mapped_noMP_prop, total_mapped_MP, total_none, key = "type", value = "count")
total_combination$type <- factor(total_combination$type, levels=c("total_none", "total_mapped_MP", "total_mapped_noMP_prop"))

Finally, I create my graphs, one for nuclear and the other for total. geom_col allows me to make bar graphs based off of heights in the data, instead of frequency, which geom_bar does. I stacked the bar plots using three proportions - mapped with mispriming, mapped without mispriming, and unmapped.

Version Author Date
3b25860 brimittleman 2019-09-04
191d71f brimittleman 2019-08-07

Version Author Date
3b25860 brimittleman 2019-09-04
191d71f brimittleman 2019-08-07

Note that the echo = FALSE parameter was added to the code chunk to prevent printing of the R code that generated the plot.

Plot the number of reads:

nuclear_melt=melt(nuclear,id.vars = c("fraction", "line"), variable.name = "read", value.name = "Number")
ggplot(nuclear_melt, aes(x=line, y=Number, fill=read))+ geom_bar(stat="identity")+ scale_fill_brewer(palette="Dark2", name = "", labels = c("unmapped", "Mapped", "Clean Mapped"))+  theme(axis.text.x = element_text( hjust = 0,vjust = 1, size = 6, angle = 90)) + labs(x="lines", y="Number of Reads", title="Number of reads mapped in Nuclear libraries")  

Version Author Date
6cfa831 brimittleman 2019-09-11
total_melt=melt(total,id.vars = c("fraction", "line"), variable.name = "read", value.name = "Number")
ggplot(total_melt, aes(x=line, y=Number, fill=read))+ geom_bar(stat="identity")+ scale_fill_brewer(palette="Dark2", name = "", labels = c("unmapped", "Mapped", "Clean Mapped"))+  theme(axis.text.x = element_text( hjust = 0,vjust = 1, size = 6, angle = 90)) + labs(x="lines", y="Number of Reads", title="Number of reads mapped in Total mRNA library")  

Version Author Date
6cfa831 brimittleman 2019-09-11

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 ggplot2_3.1.1  tidyr_0.8.3    dplyr_0.8.0.1 

loaded via a namespace (and not attached):
 [1] Rcpp_1.0.2         RColorBrewer_1.1-2 pillar_1.3.1      
 [4] compiler_3.5.1     later_0.7.5        git2r_0.26.1      
 [7] plyr_1.8.4         workflowr_1.6.0    tools_3.5.1       
[10] digest_0.6.18      evaluate_0.12      tibble_2.1.1      
[13] gtable_0.2.0       pkgconfig_2.0.2    rlang_0.4.0       
[16] yaml_2.2.0         withr_2.1.2        stringr_1.3.1     
[19] knitr_1.20         fs_1.3.1           rprojroot_1.3-2   
[22] grid_3.5.1         tidyselect_0.2.5   glue_1.3.0        
[25] R6_2.3.0           rmarkdown_1.10     purrr_0.3.2       
[28] magrittr_1.5       whisker_0.3-2      backports_1.1.2   
[31] scales_1.0.0       promises_1.0.1     htmltools_0.3.6   
[34] assertthat_0.2.0   colorspace_1.3-2   httpuv_1.4.5      
[37] labeling_0.3       stringi_1.2.4      lazyeval_0.2.1    
[40] munsell_0.5.0      crayon_1.3.4