Last updated: 2020-05-20

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Knit directory: Comparative_APA/analysis/

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Unstaged changes:
    Modified:   analysis/DeandNumPAS.Rmd
    Modified:   analysis/DiffTop2SecondDom.Rmd
    Modified:   analysis/DirSelectionKhan.Rmd
    Modified:   analysis/ExploredAPA.Rmd
    Modified:   analysis/MMExpreiment.Rmd
    Modified:   analysis/OppositeMap.Rmd
    Modified:   analysis/PTM_analysis.Rmd
    Modified:   analysis/TotalDomStructure.Rmd
    Modified:   analysis/TotalVNuclearBothSpecies.Rmd
    Modified:   analysis/annotationInfo.Rmd
    Modified:   analysis/changeMisprimcut.Rmd
    Modified:   analysis/comp2apaQTLPAS.Rmd
    Modified:   analysis/correlationPhenos.Rmd
    Modified:   analysis/dInforContent.Rmd
    Modified:   analysis/diffExpression.Rmd
    Modified:   analysis/establishCutoffs.Rmd
    Modified:   analysis/investigatePantro5.Rmd
    Modified:   analysis/mRNADecay.Rmd
    Modified:   analysis/miRNAanalysis.Rmd
    Modified:   analysis/multiMap.Rmd
    Modified:   analysis/phastCon.Rmd
    Modified:   analysis/pol2.Rmd
    Modified:   analysis/signalsites_doublefilter.Rmd
    Modified:   analysis/speciesSpecific.Rmd

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Rmd 193632e brimittleman 2020-05-20 add expression levels by dapa and direction 
library(workflowr)
This is workflowr version 1.6.0
Run ?workflowr for help getting started
library(ggpubr)
Loading required package: ggplot2
Loading required package: magrittr
library(tidyverse)
── Attaching packages ─────────────────────── tidyverse 1.2.1 ──
✔ tibble  2.1.1       ✔ purrr   0.3.2  
✔ tidyr   0.8.3       ✔ dplyr   0.8.0.1
✔ readr   1.3.1       ✔ stringr 1.3.1  
✔ tibble  2.1.1       ✔ forcats 0.3.0  
── Conflicts ────────────────────────── tidyverse_conflicts() ──
✖ tidyr::extract()   masks magrittr::extract()
✖ dplyr::filter()    masks stats::filter()
✖ dplyr::lag()       masks stats::lag()
✖ purrr::set_names() masks magrittr::set_names()

I want to characterize expression levels in general for the conserved and dAPA genes.

Meta=read.table("../data/PAS_doubleFilter/PAS_5perc_either_HumanCoord_BothUsage_meta_doubleFilter.txt", header = T, stringsAsFactors = F) 


Meta_genes= Meta %>% select(gene) %>% unique()

Meta_PAS=Meta %>%  select(PAS,gene)

dAPAGenes=read.table("../data/DiffIso_Nuclear_DF/SignifianceEitherGENES_Nuclear.txt", header = T, stringsAsFactors = F)
dAPAPAS=read.table("../data/DiffIso_Nuclear_DF/AllPAS_withGeneSig.txt", header = T, stringsAsFactors = F) %>% inner_join(Meta, by=c("chr","start", "end","gene")) %>% select(PAS,gene,SigPAU2 ) 

dAPAPAS_genes= dAPAPAS %>% select(gene) %>% unique()

dAPATestedGenes= dAPAPAS  %>% select(gene) %>% unique() %>% mutate(dAPA=ifelse(gene %in% dAPAGenes$gene,"Yes", "No"))
dICdata= read.table("../data/IndInfoContent/SimpsonMedianSignificance.txt", header = T, stringsAsFactors = F)%>% select(sIC,gene)
dICdata_sig= dICdata %>% filter(sIC=="Yes")
dAPAandDic= dICdata %>% inner_join(dAPATestedGenes,by="gene") %>% mutate(Both=ifelse(sIC=="Yes" & dAPA=="Yes", "Yes","No"),OnlyIC=ifelse(sIC=="Yes" & dAPA=="No", "Yes","No"),OnlyAPA=ifelse(sIC=="No" & dAPA=="Yes", "Yes","No"))


OnlyAPAGenes= dAPAandDic %>% filter(OnlyAPA=="Yes") %>% select(gene) %>% mutate(set="Site")
IsoformGenes=  dAPAandDic %>% filter(OnlyIC=="Yes") %>% select(gene) %>% mutate(set="Isoform")
BothGenes=  dAPAandDic %>% filter(Both=="Yes") %>% select(gene) %>% mutate(set="Both")
NoneGenes=dAPAandDic %>% filter(dAPA=="No" & sIC=="No" ) %>% select(gene) %>% mutate(set="Conserved")


CharacterizeAllGenes= OnlyAPAGenes %>% bind_rows(IsoformGenes) %>% bind_rows(BothGenes)%>% bind_rows(BothGenes) %>% bind_rows(NoneGenes)

Join with the expression data:

nameID=read.table("../../genome_anotation_data/ensemble_to_genename.txt",sep="\t", header = T, stringsAsFactors = F) %>% dplyr::select(Gene_stable_ID, Gene.name)
Expression=read.table("../data/DiffExpression/NoramalizedExpression.txt",stringsAsFactors = F,header = T, col.names = c("Gene_stable_ID" ,"Chimp", "Human" )) %>% inner_join(nameID,by="Gene_stable_ID") %>% dplyr::rename('gene'=Gene.name)  %>% select(-Gene_stable_ID)

CharacterizeAllGenesExp=CharacterizeAllGenes %>% inner_join(Expression, by="gene") %>% gather("Species", "Expression", -gene, -set ) %>% mutate(OverAllCons=ifelse(set=="Conserved", "Yes","No"))

Plot human:

ggplot(CharacterizeAllGenesExp, aes(x=set, y=Expression, fill=set))+geom_boxplot() + facet_grid(~Species) + stat_compare_means() + scale_fill_brewer(palette = "RdYlBu") +labs(x="APA conservation state", y="Normalized Expression")

ggplot(CharacterizeAllGenesExp, aes(x=OverAllCons, y=Expression, fill=OverAllCons))+geom_boxplot() + facet_grid(~Species) + stat_compare_means() + scale_fill_brewer(palette = "Set1") + labs(x="Is gene conserved on all APA levels", y="Normalized Expression") + theme(legend.position="none")


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] forcats_0.3.0   stringr_1.3.1   dplyr_0.8.0.1   purrr_0.3.2    
 [5] readr_1.3.1     tidyr_0.8.3     tibble_2.1.1    tidyverse_1.2.1
 [9] ggpubr_0.2      magrittr_1.5    ggplot2_3.1.1   workflowr_1.6.0

loaded via a namespace (and not attached):
 [1] tidyselect_0.2.5   reshape2_1.4.3     haven_1.1.2       
 [4] lattice_0.20-38    colorspace_1.3-2   generics_0.0.2    
 [7] htmltools_0.3.6    yaml_2.2.0         rlang_0.4.0       
[10] later_0.7.5        pillar_1.3.1       glue_1.3.0        
[13] withr_2.1.2        RColorBrewer_1.1-2 modelr_0.1.2      
[16] readxl_1.1.0       plyr_1.8.4         munsell_0.5.0     
[19] gtable_0.2.0       cellranger_1.1.0   rvest_0.3.2       
[22] evaluate_0.12      labeling_0.3       knitr_1.20        
[25] httpuv_1.4.5       broom_0.5.1        Rcpp_1.0.4.6      
[28] promises_1.0.1     scales_1.0.0       backports_1.1.2   
[31] jsonlite_1.6       fs_1.3.1           hms_0.4.2         
[34] digest_0.6.18      stringi_1.2.4      grid_3.5.1        
[37] rprojroot_1.3-2    cli_1.1.0          tools_3.5.1       
[40] lazyeval_0.2.1     crayon_1.3.4       whisker_0.3-2     
[43] pkgconfig_2.0.2    xml2_1.2.0         lubridate_1.7.4   
[46] assertthat_0.2.0   rmarkdown_1.10     httr_1.3.1        
[49] rstudioapi_0.10    R6_2.3.0           nlme_3.1-137      
[52] git2r_0.26.1       compiler_3.5.1