Last updated: 2020-05-01

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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/ExploredAPA.Rmd
    Modified:   analysis/ExploredAPA_DF.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/establishCutoffs.Rmd
    Modified:   analysis/investigatePantro5.Rmd
    Modified:   analysis/mRNADecay.Rmd
    Modified:   analysis/multiMap.Rmd
    Modified:   analysis/pol2.Rmd
    Modified:   analysis/signalsites_doublefilter.Rmd
    Modified:   analysis/speciesSpecific.Rmd

Note that any generated files, e.g. HTML, png, CSS, etc., are not included in this status report because it is ok for generated content to have uncommitted changes.


These are the previous versions of the R Markdown and HTML files. If you’ve configured a remote Git repository (see ?wflow_git_remote), click on the hyperlinks in the table below to view them.

File Version Author Date Message
Rmd c78e612 brimittleman 2020-05-01 add dic with others

I used simpson to call differences in information content.

library(workflowr)
This is workflowr version 1.6.0
Run ?workflowr for help getting started
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────────── tidyverse 1.2.1 ──
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── Conflicts ───────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag()    masks stats::lag()

I want to look at DE, dP, dt, dAPA, and dIC. I will do simple 2by2 tables at first.

For each set I will only consider the genes that I can test for those analylsis.

Load all set:

APA

Meta=read.table("../data/PAS_doubleFilter/PAS_5perc_either_HumanCoord_BothUsage_meta_doubleFilter.txt", header = T, stringsAsFactors = F)  %>% dplyr::select(PAS, chr, start,end, loc)
DiffIso= read.table("../data/DiffIso_Nuclear_DF/AllPAS_withGeneSig.txt", header = T,stringsAsFactors = F) %>% inner_join(Meta, by=c("chr", 'start','end')) 

#gene level:  

SigGenesDI=read.table("../data/DiffIso_Nuclear_DF/SignifianceEitherGENES_Nuclear.txt",header = T,stringsAsFactors = F)
DiffIsoGene= DiffIso %>% select(gene) %>% unique() %>% mutate(dAPA=ifelse(gene %in% SigGenesDI$gene, "Yes", "No"))


DiffIsoGene %>% group_by(dAPA) %>% summarise(n())
# A tibble: 2 x 2
  dAPA  `n()`
  <chr> <int>
1 No     6717
2 Yes    1705

DE

nameID=read.table("../../genome_anotation_data/ensemble_to_genename.txt",sep="\t", header = T, stringsAsFactors = F) %>% dplyr::select(Gene_stable_ID, Gene.name)

DiffExp=read.table("../data/DiffExpression/DEtested_allres.txt",stringsAsFactors = F,header = F, col.names = c("Gene_stable_ID" ,"logFC" ,"AveExpr" , "t" ,  "P.Value" ,  "adj.P.Val", "B"  )) %>% inner_join(nameID,by="Gene_stable_ID") %>% dplyr::rename('gene'=Gene.name) %>% dplyr::select(-Gene_stable_ID) %>% mutate(DE=ifelse(adj.P.Val<.05, "Yes", "No"))


DiffExp %>% group_by(DE) %>% summarise(n())
# A tibble: 2 x 2
  DE    `n()`
  <chr> <int>
1 No     6356
2 Yes    3794
DiffExpSmall= DiffExp %>% select(gene,DE)

DTE

Ribo=read.table("../data/Wang_ribo/Additionaltable5_translationComparisons.txt",header = T, stringsAsFactors = F) %>% rename("Gene_stable_ID"= ENSG) %>% inner_join(nameID,by="Gene_stable_ID") %>% dplyr::select(Gene.name, HvC.beta, HvC.pvalue, HvC.FDR) %>% rename("gene"=Gene.name) %>% mutate(dTE=ifelse(HvC.FDR <0.05, "Yes","No"))


Ribo %>% group_by(dTE) %>% summarise(n())
# A tibble: 2 x 2
  dTE   `n()`
  <chr> <int>
1 No     7236
2 Yes    1993
RiboSmall= Ribo %>% select(gene,dTE)

DP
(pval is adjusted already)

Prot= read.table("../data/Khan_prot/ProtData_effectSize.txt",header = T)  %>% mutate(dP=ifelse(pval<0.05, "Yes", "No"))

Prot %>% group_by(dP) %>% summarise(n())
# A tibble: 2 x 2
  dP    `n()`
  <chr> <int>
1 No     2004
2 Yes    1266
ProtSmall=Prot %>% select(gene, dP)

Simpson Info Content

dICdata= read.table("../data/IndInfoContent/SimpsonMedianSignificance.txt", header = T, stringsAsFactors = F) %>% rename(dIC=sIC)

dICdata %>% group_by(dIC) %>% summarise(n())
# A tibble: 2 x 2
  dIC   `n()`
  <chr> <int>
1 No     7570
2 Yes     881
dICSmall=dICdata %>% select(gene, dIC)

dAPA and dIC

I will start with dIC and dAPA, I expect a pretty high overlap for this.

dICanddAPA= dICSmall %>% inner_join(DiffIsoGene, by="gene") 


dICanddAPA22=dICanddAPA %>% group_by(dIC, dAPA) %>% summarise(n=n()) %>% spread(dAPA, n) %>% column_to_rownames("dIC")
dICanddAPA22
      No  Yes
No  6291 1251
Yes  426  454
#top is dIC, side is dAPA

Do this with proportion:

dICanddAPA %>% group_by(dIC, dAPA) %>% summarise(n=n()) %>% mutate(nG=nrow(dICanddAPA),Prop=n/nG)  %>% select(dIC, dAPA, Prop) %>% spread(dAPA, Prop)
# A tibble: 2 x 3
# Groups:   dIC [2]
  dIC       No    Yes
  <chr>  <dbl>  <dbl>
1 No    0.747  0.149 
2 Yes   0.0506 0.0539

Enrichment:

x=nrow(dICanddAPA %>% filter(dIC=="Yes", dAPA=="Yes"))
m=nrow(dICanddAPA %>% filter(dAPA=="Yes"))
n=nrow(dICanddAPA %>% filter(dAPA=="No"))
k=nrow(dICanddAPA %>% filter(dIC=="Yes"))
N=nrow(dICanddAPA)
phyper(x-1,m,n,k,lower.tail=F)
[1] 1.812359e-108
(x/k)/(m/N)
[1] 2.548379

dE and dIC

I will start with dIC and dAPA, I expect a pretty high overlap for this.

dICanddE= dICSmall %>% inner_join(DiffExpSmall, by="gene") 


dICanddE22=dICanddE %>% group_by(dIC, DE) %>% summarise(n=n()) %>% spread(DE, n) %>% column_to_rownames("dIC")
dICanddE22
      No  Yes
No  4233 2464
Yes  466  317
#top is dIC, side is DE

Do this with proportion:

dICanddE %>% group_by(dIC, DE) %>% summarise(n=n()) %>% mutate(nG=nrow(dICanddE),Prop=n/nG)  %>% select(dIC, DE, Prop) %>% spread(DE, Prop)
# A tibble: 2 x 3
# Groups:   dIC [2]
  dIC       No    Yes
  <chr>  <dbl>  <dbl>
1 No    0.566  0.329 
2 Yes   0.0623 0.0424
x=nrow(dICanddE %>% filter(dIC=="Yes", DE=="Yes"))
m=nrow(dICanddE %>% filter(DE=="Yes"))
n=nrow(dICanddE %>% filter(DE=="No"))
k=nrow(dICanddE %>% filter(dIC=="Yes"))
N=nrow(dICanddE)
phyper(x-1,m,n,k,lower.tail=F)
[1] 0.02402776
(x/k)/(m/N)
[1] 1.088925

dT and dIC

I will start with dIC and dAPA, I expect a pretty high overlap for this.

dICanddT= dICSmall %>% inner_join(RiboSmall, by="gene") 


dICanddT22=dICanddT %>% group_by(dIC, dTE) %>% summarise(n=n()) %>% spread(dTE, n) %>% column_to_rownames("dIC")
dICanddT22
      No  Yes
No  4557 1241
Yes  504  185
#top is dIC, side is dTE

Do this with proportion:

dICanddT %>% group_by(dIC, dTE) %>% summarise(n=n()) %>% mutate(nG=nrow(dICanddT),Prop=n/nG)  %>% select(dIC, dTE, Prop) %>% spread(dTE, Prop)
# A tibble: 2 x 3
# Groups:   dIC [2]
  dIC       No    Yes
  <chr>  <dbl>  <dbl>
1 No    0.702  0.191 
2 Yes   0.0777 0.0285
x=nrow(dICanddT %>% filter(dIC=="Yes", dTE=="Yes"))
m=nrow(dICanddT %>% filter(dTE=="Yes"))
n=nrow(dICanddT %>% filter(dTE=="No"))
k=nrow(dICanddT %>% filter(dIC=="Yes"))
N=nrow(dICanddT)
phyper(x-1,m,n,k,lower.tail=F)
[1] 0.0008020285
(x/k)/(m/N)
[1] 1.221453

dP and dIC

I will start with dIC and dAPA, I expect a pretty high overlap for this.

dICanddP= dICSmall %>% inner_join(ProtSmall, by="gene") 
Warning: Column `gene` joining character vector and factor, coercing into
character vector
dICanddP22=dICanddP %>% group_by(dIC, dP) %>% summarise(n=n()) %>% spread(dP, n) %>% column_to_rownames("dIC")
dICanddP22
      No Yes
No  1386 909
Yes  224 124
#top is dIC, side is DP

Do this with proportion:

dICanddP %>% group_by(dIC, dP) %>% summarise(n=n()) %>% mutate(nG=nrow(dICanddP),Prop=n/nG)  %>% select(dIC, dP, Prop) %>% spread(dP, Prop)
# A tibble: 2 x 3
# Groups:   dIC [2]
  dIC       No    Yes
  <chr>  <dbl>  <dbl>
1 No    0.524  0.344 
2 Yes   0.0848 0.0469
x=nrow(dICanddP %>% filter(dIC=="Yes", dP=="Yes"))
m=nrow(dICanddP %>% filter(dP=="Yes"))
n=nrow(dICanddP %>% filter(dP=="No"))
k=nrow(dICanddP %>% filter(dIC=="Yes"))
N=nrow(dICanddP)
phyper(x-1,m,n,k,lower.tail=F)
[1] 0.9304879
(x/k)/(m/N)
[1] 0.9116734

Not enough power for this one.


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    ggplot2_3.1.1  
 [9] tidyverse_1.2.1 workflowr_1.6.0

loaded via a namespace (and not attached):
 [1] tidyselect_0.2.5 haven_1.1.2      lattice_0.20-38  colorspace_1.3-2
 [5] generics_0.0.2   htmltools_0.3.6  yaml_2.2.0       utf8_1.1.4      
 [9] rlang_0.4.0      later_0.7.5      pillar_1.3.1     glue_1.3.0      
[13] withr_2.1.2      modelr_0.1.2     readxl_1.1.0     plyr_1.8.4      
[17] munsell_0.5.0    gtable_0.2.0     cellranger_1.1.0 rvest_0.3.2     
[21] evaluate_0.12    knitr_1.20       httpuv_1.4.5     fansi_0.4.0     
[25] broom_0.5.1      Rcpp_1.0.4.6     promises_1.0.1   scales_1.0.0    
[29] backports_1.1.2  jsonlite_1.6     fs_1.3.1         hms_0.4.2       
[33] digest_0.6.18    stringi_1.2.4    grid_3.5.1       rprojroot_1.3-2 
[37] cli_1.1.0        tools_3.5.1      magrittr_1.5     lazyeval_0.2.1  
[41] crayon_1.3.4     whisker_0.3-2    pkgconfig_2.0.2  xml2_1.2.0      
[45] lubridate_1.7.4  assertthat_0.2.0 rmarkdown_1.10   httr_1.3.1      
[49] rstudioapi_0.10  R6_2.3.0         nlme_3.1-137     git2r_0.26.1    
[53] compiler_3.5.1