Last updated: 2020-01-15
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Knit directory: Comparative_APA/analysis/
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Unstaged changes:
Modified: analysis/OppositeMap.Rmd
Modified: analysis/annotationInfo.Rmd
Modified: analysis/investigatePantro5.Rmd
Modified: analysis/multiMap.Rmd
Modified: analysis/speciesSpecific.Rmd
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 446243e | brimittleman | 2020-01-16 | update issue |
html | 0a3545a | brimittleman | 2020-01-15 | Build site. |
Rmd | 5dd5e35 | brimittleman | 2020-01-15 | add code to viz nuclear dapa |
library(workflowr)
This is workflowr version 1.5.0
Run ?workflowr for help getting started
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──
✔ ggplot2 3.1.1 ✔ purrr 0.3.2
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── Conflicts ───────────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
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I want to write a loop that will create boxplots for all of the PAS in each gene. I need a script that takes one gene and then outputs the plot.
I want PAS:Location as the x axis. Usage as the y axis. I will seperate the plots by species.
I need a long dataframe with species, individual, PASid, gene, usage.
Pull in the usage numbers:
../data/Pheno_5perc_nuclear/ALLPAS_postLift_LocParsed_bothSpecies_pheno_5perc_Nuclear.txt.gz
I need to make these numeric.
mkdir ../data/files4viz_nuclear/
Vector with humans:
humans=c('NA18498', 'NA18499', 'NA18502' ,'NA18504', 'NA18510', 'NA18523')
chimps=c( 'NA18358', 'NA3622' ,'NA3659', 'NA4973', 'NApt30', 'NApt91')
LOC100288069_+_utr3-Both-human23
LOC107984841_+_utr3-Chimp-chimp242477 utr3-Chimp-chimp242477
NuclearUsage=read.table("../data/Pheno_5perc_nuclear/ALLPAS_postLift_LocParsed_bothSpecies_pheno_5perc_Nuclear.txt.gz", header = T)
Nuclear_gather=NuclearUsage %>% gather(key="Ind", value="Frac", -chrom) %>% separate(Frac, into=c("num", "denom"), sep="/") %>% mutate(numUsage=as.integer(num)/as.integer(denom)) %>% replace_na(list(numUsage=0)) %>% separate(Ind, into=c("sample", "fraction"), by="_") %>% mutate(species=ifelse(sample %in% humans, "Human","Chimp")) %>% separate(chrom, into=c("chr","start","end","PASid"), sep=":")%>% separate(PASid, into=c("Gene", "strand", "PASinf"), sep="_") %>% separate(PASinf, into=c("loc", "disc", "PASnum"), sep="-")%>% mutate(PAS=paste(PASnum,loc,sep="_")) %>% dplyr::select(chr,start,end, strand, PAS, species,Gene, sample,numUsage)
Warning: attributes are not identical across measure variables;
they will be dropped
example gene:
DFFB
Nuclear_gather_DFFB=Nuclear_gather %>% filter(Gene=="DFFB")
Nuclear_gather_DFFB$start=as.factor(as.integer(Nuclear_gather_DFFB$start))
ggplot(Nuclear_gather_DFFB,aes(x=start, y=numUsage, by=species, fill=species))+ geom_boxplot() + scale_fill_brewer(palette = "Dark2")+theme(axis.text.x = element_text(angle = 90)) + labs(y="Usage", title="Usage by species for DFFB")
Version | Author | Date |
---|---|---|
0a3545a | brimittleman | 2020-01-15 |
write.table(Nuclear_gather,"../data/files4viz_nuclear/NuclearPASUsage.txt", col.names = T, row.names = F, quote = F)
I will put this in an R script that takes a gene.
test on DFFB
Rscript PlotNuclearUsagebySpecies.R -g DFFB
This works, now I can make it for every gene that was called as DAPA. I will make a list of all of the genes.
genes are in ../data/DiffIso_Nuclear/SignifianceEitherGENES_Nuclear.txt
sed '1d' ../data/DiffIso_Nuclear/SignifianceEitherGENES_Nuclear.txt > ../data/DiffIso_Nuclear/SignifianceEitherGENES_Nuclear_noHead.txt
sbatch makeNuclearDapaplots.sh
Problem is with the order. The chimp PAS come before the other. This mean they are not in line. I need to pull the locations into the file and do some factor ordering.
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
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[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_1.5.0
loaded via a namespace (and not attached):
[1] tidyselect_0.2.5 haven_1.1.2 lattice_0.20-38
[4] colorspace_1.3-2 generics_0.0.2 htmltools_0.3.6
[7] yaml_2.2.0 rlang_0.4.0 later_0.7.5
[10] pillar_1.3.1 glue_1.3.0 withr_2.1.2
[13] RColorBrewer_1.1-2 modelr_0.1.2 readxl_1.1.0
[16] plyr_1.8.4 munsell_0.5.0 gtable_0.2.0
[19] cellranger_1.1.0 rvest_0.3.2 evaluate_0.12
[22] labeling_0.3 knitr_1.20 httpuv_1.4.5
[25] broom_0.5.1 Rcpp_1.0.2 promises_1.0.1
[28] scales_1.0.0 backports_1.1.2 jsonlite_1.6
[31] fs_1.3.1 hms_0.4.2 digest_0.6.18
[34] stringi_1.2.4 grid_3.5.1 rprojroot_1.3-2
[37] cli_1.1.0 tools_3.5.1 magrittr_1.5
[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