Last updated: 2019-06-13
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Knit directory: apaQTL/analysis/
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Unstaged changes:
Modified: analysis/Readdistagainstfeatures.Rmd
Modified: analysis/index.Rmd
Modified: analysis/motifDisruption.Rmd
Modified: analysis/nascenttranscription.Rmd
Modified: analysis/nucintronicanalysis.Rmd
Modified: analysis/overlapapaqtlsandeqtls.Rmd
Modified: analysis/rna_netseq_h3k12ac.Rmd
Modified: code/BothFracDTPlotGeneRegions.sh
Modified: code/Snakefile
Deleted: code/Upstream10Bases_general.py
Modified: code/apaQTLCorrectPvalMakeQQ.R
Modified: code/apaQTL_Nominal.sh
Modified: code/apaQTL_permuted.sh
Modified: code/apaQTLsnake.err
Modified: code/bam2bw.sh
Modified: code/bed2saf.py
Modified: code/cluster.json
Modified: code/clusterfiltPAS.json
Modified: code/config.yaml
Modified: code/environment.yaml
Modified: code/makePheno.py
Deleted: code/test.txt
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File | Version | Author | Date | Message |
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Rmd | 2d7b2ec | brimittleman | 2019-06-13 | fix bug |
html | bf3a1e0 | brimittleman | 2019-05-14 | Build site. |
Rmd | 77ca26a | brimittleman | 2019-05-14 | results by logef |
library(workflowr)
This is workflowr version 1.3.0
Run ?workflowr for help getting started
library(tidyverse)
── Attaching packages ─────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──
✔ ggplot2 3.1.1 ✔ 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(reshape2)
Attaching package: 'reshape2'
The following object is masked from 'package:tidyr':
smiths
PAS=read.table("../data/peaks_5perc/APApeaks.ALLChrom.Filtered.Named.GeneLocAnnoPARSED.5percCov.bothfrac.SAF",stringsAsFactors = F,header = T) %>% separate(GeneID, into=c("num", "chr", "start", "end", "strand", "geneID"), sep=":") %>% separate(geneID, into=c("gene", "loc"),sep="_") %>% mutate(intron=paste("chr", Chr, ":", Start, ":", End, ":", gene,sep="")) %>% select(intron, loc)
PAS_loc =PAS%>% group_by(loc) %>% summarise(nloc=n())
effectsize=read.table("../data/DiffIso/TN_diff_isoform_allChrom.txt_effect_sizes.txt", stringsAsFactors = F, col.names=c('intron', 'logef' ,'Nuclear', 'Total','deltaPAU')) %>% filter(intron != "intron") %>% filter(logef>.5)
I want to create a data frame that has the location proportion distribution based on different \(\Delta\) PAU. 0-.1 .1-.2 .2-.3 .3-.4 .4-.5 >.5
First I will seperate the total and nuclear but the sign of the \(\Delta\) PAU.
Total_dpau= effectsize %>% filter(deltaPAU > 0) %>% inner_join(PAS, by="intron") %>% select(-logef, -Nuclear,-Total) %>% mutate(fraction="Total", PAU_Cat=ifelse(deltaPAU <.1, "<.1", ifelse(deltaPAU >=.1 & deltaPAU <.2, "<.2", ifelse(deltaPAU >=.2 & deltaPAU <.3, "<.3", ifelse(deltaPAU >=.3 & deltaPAU <.4, "<.4", "<.5")))))
Nuclear_dpau= effectsize %>% filter(deltaPAU <0) %>% inner_join(PAS, by="intron") %>% select(-logef,-Nuclear,-Total) %>% mutate(fraction="Nuclear", PAU_Cat=ifelse(deltaPAU >-.1, "<.1", ifelse(deltaPAU <=-.1 & deltaPAU > -.2, "<.2", ifelse(deltaPAU <=-.2 & deltaPAU >-.3, "<.3", ifelse(deltaPAU <=-.3 & deltaPAU >-.4, "<.4", "<.5")))))
Merge these together to start grouping:
allPAU=as.data.frame(rbind(Total_dpau, Nuclear_dpau)) %>% group_by(fraction, PAU_Cat, loc ) %>% summarise(nperLoc=n()) %>% full_join(PAS_loc, by ="loc") %>% mutate(Prop=nperLoc/nloc)
Proportion within group:
allPAU_ingroup= allPAU %>% mutate(nCat=sum(nperLoc),proppercat=nperLoc/nCat)
ggplot(allPAU_ingroup, aes(x=loc,y=proppercat, group=fraction, fill=fraction)) + geom_bar(stat="identity", position = "dodge") + facet_wrap(~PAU_Cat)+ scale_fill_manual(values=c("deepskyblue3","darkviolet")) + theme(axis.text.x = element_text(angle = 90, hjust = 1)) + labs(title="Proportion of PAS by location and delta PAU \n logef >.5")
Version | Author | Date |
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bf3a1e0 | brimittleman | 2019-05-14 |
I need to pull in the TSS information so I can look at the distance between the differentially used peaks and by distance .
tss=read.table("../../genome_anotation_data/refseq.ProteinCoding.bed",col.names = c("chrom", "start", "end", "gene", "score", "strand") ,stringsAsFactors = F) %>% mutate(TSS= ifelse(strand=="+", start, end)) %>% select(gene, TSS, strand)
Seperate effect size introns:
PAS base for + strand is end, PAS for neg stand in -
effectsize_TSS= effectsize %>% separate(intron, into=c("chrom", "start", "end", "gene"),sep=":") %>% mutate(fraction=ifelse(deltaPAU < 0, "nuclear", "total")) %>% inner_join(tss, by="gene") %>% mutate(dist2PAS=ifelse(strand=="+", as.numeric(end)-as.numeric(TSS), as.numeric(TSS)-as.numeric(start)))
effectsize_TSS_tot= effectsize_TSS %>% filter(fraction=="total") %>% mutate( PAU_Cat=ifelse(deltaPAU <.1, "<.1", ifelse(deltaPAU >=.1 & deltaPAU <.2, "<.2", ifelse(deltaPAU >=.2 & deltaPAU <.3, "<.3", ifelse(deltaPAU >=.3 & deltaPAU <.4, "<.4", "<.5")))))
effectsize_TSS_nuc=effectsize_TSS %>% filter(fraction=="nuclear") %>% mutate( PAU_Cat=ifelse(deltaPAU >-.1, "<.1", ifelse(deltaPAU <=-.1 & deltaPAU > -.2, "<.2", ifelse(deltaPAU <=-.2 & deltaPAU >-.3, "<.3", ifelse(deltaPAU <=-.3 & deltaPAU >-.4, "<.4", "<.5")))))
effectsize_TSS_cat=as.data.frame(rbind(effectsize_TSS_tot, effectsize_TSS_nuc)) %>% filter(dist2PAS >0)
ggplot(effectsize_TSS_cat, aes(x=log10(dist2PAS), by=fraction, fill=fraction))+ geom_density(alpha=.4) + facet_grid(~PAU_Cat) + labs(title="Distance to TSS for differentialy used PAS \n logef >.5")+scale_fill_manual(values=c("deepskyblue3","darkviolet"))
Warning: Groups with fewer than two data points have been dropped.
Version | Author | Date |
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bf3a1e0 | brimittleman | 2019-05-14 |
length=read.table("../../genome_anotation_data/refseq.ProteinCoding.bed",col.names = c("chrom", "start", "end", "gene", "score", "strand") ,stringsAsFactors = F) %>% mutate(length=abs(end-start)) %>% mutate(TSS= ifelse(strand=="+", start, end)) %>% select(gene, length,TSS, strand)
effectsize_length= effectsize %>% separate(intron, into=c("chrom", "start", "end", "gene"),sep=":") %>% mutate(fraction=ifelse(deltaPAU < 0, "nuclear", "total")) %>% inner_join(length, by="gene") %>% mutate(PercLength=ifelse(strand=="+", ((as.numeric(end)-as.numeric(TSS))/as.numeric(length)), (1-(as.numeric(start)-as.numeric(TSS))/as.numeric(length))))
effectsize_length_tot= effectsize_length %>% filter(fraction=="total") %>% mutate( PAU_Cat=ifelse(deltaPAU <.1, "<.1", ifelse(deltaPAU >=.1 & deltaPAU <.2, "<.2", ifelse(deltaPAU >=.2 & deltaPAU <.3, "<.3", ifelse(deltaPAU >=.3 & deltaPAU <.4, "<.4", "<.5")))))
effectsize_length_nuc=effectsize_length %>% filter(fraction=="nuclear") %>% mutate( PAU_Cat=ifelse(deltaPAU >-.1, "<.1", ifelse(deltaPAU <=-.1 & deltaPAU > -.2, "<.2", ifelse(deltaPAU <=-.2 & deltaPAU >-.3, "<.3", ifelse(deltaPAU <=-.3 & deltaPAU >-.4, "<.4", "<.5")))))
effectsize_length_cat=as.data.frame(rbind(effectsize_length_tot, effectsize_length_nuc)) %>% filter(PercLength<=1 & PercLength >0)
effectsize_length_catall=as.data.frame(rbind(effectsize_length_tot, effectsize_length_nuc))
ggplot(effectsize_length_cat, aes(x=PercLength, by=fraction, fill=fraction))+ geom_histogram(alpha=.4,bins=10) + facet_grid(~PAU_Cat) + labs(title="Location of differentially used PAS within a gene body \n logef >.5")+scale_fill_manual(values=c("deepskyblue3","darkviolet"))
Version | Author | Date |
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bf3a1e0 | brimittleman | 2019-05-14 |
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 forcats_0.3.0 stringr_1.3.1 dplyr_0.8.0.1
[5] purrr_0.3.2 readr_1.3.1 tidyr_0.8.3 tibble_2.1.1
[9] ggplot2_3.1.1 tidyverse_1.2.1 workflowr_1.3.0
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_0.25.2 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