Last updated: 2019-11-12
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Knit directory: apaQTL/analysis/
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Unstaged changes:
Modified: analysis/NuclearSpecIncludeNotTested.Rmd
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Modified: code/apaQTLsnake.err
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Deleted: reads_graphs.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.
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | d8c08ab | brimittleman | 2019-11-12 | add enrichment |
html | 8a3d1ea | brimittleman | 2019-11-08 | Build site. |
Rmd | d72c604 | brimittleman | 2019-11-08 | add first intron analysis |
Check for enrichment in first intron.
This uses files created in the verifyFirstintronresult analysis.
library(workflowr)
This is workflowr version 1.4.0
Run ?workflowr for help getting started
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──
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✔ tibble 2.1.1 ✔ dplyr 0.8.0.1
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── Conflicts ───────────────────────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
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library(reshape2)
Attaching package: 'reshape2'
The following object is masked from 'package:tidyr':
smiths
pas2intron= read.table( "../data/intron_analysis/NuclearIntronPASwithWhichintron.txt", stringsAsFactors = F, header = T)
I need to know how many 1st introns there are, how many second introns there are…
The number of introns in these genes is in the nintron column.
I can group the number of genes with each number of introns.
pas2intron_genes= pas2intron %>% select(gene, nintron) %>% unique() %>% group_by(nintron) %>% summarize(nGenes=n())
head(pas2intron_genes)
# A tibble: 6 x 2
nintron nGenes
<int> <int>
1 3 393
2 4 401
3 5 408
4 6 385
5 7 362
6 8 340
I want to add these numbers but only include below. For example, all of these have 1 intron, only those above 5 have 5 introns.
Do this manually for 1-10 first.
n1intron=sum(pas2intron_genes$nGenes)
n2intron=sum(pas2intron_genes$nGenes)
n3intron=sum(pas2intron_genes$nGenes)
n4intron= pas2intron_genes %>% filter(nintron >=4)
n5intron= pas2intron_genes %>% filter(nintron >=5)
n6intron= pas2intron_genes %>% filter(nintron >=6)
n7intron= pas2intron_genes %>% filter(nintron >=7)
n8intron= pas2intron_genes %>% filter(nintron >=8)
n9intron= pas2intron_genes %>% filter(nintron >=9)
n10intron= pas2intron_genes %>% filter(nintron >=10)
nGenesum=c(n1intron,n2intron,n3intron, sum(n4intron$nGenes),sum(n5intron$nGenes),sum(n6intron$nGenes),sum(n7intron$nGenes),sum(n8intron$nGenes),sum(n9intron$nGenes),sum(n10intron$nGenes))
pas2intron_intron_grouped=pas2intron %>% group_by(Intronid) %>% summarise(nBin=n(), meanSize=mean(intronLength)) %>% mutate(normNBin=nBin/meanSize)
pas2intron_intron_grouped_small=pas2intron_intron_grouped %>% filter(Intronid <=10)
pas2intron_intron_grouped_small_withnintron=as.data.frame(cbind(pas2intron_intron_grouped_small, nGenesum)) %>% mutate(NormbylengthandN=normNBin/nGenesum)
ggplot(pas2intron_intron_grouped_small_withnintron, aes(x=Intronid, y=NormbylengthandN)) +geom_bar(stat="identity") + labs(title="PAS by Intron \n normalized by intron mean length and number of introns tested", y="normalized number in intron category", x="intron category")
Version | Author | Date |
---|---|---|
8a3d1ea | brimittleman | 2019-11-08 |
Assess enrichment based on introns 1-10 with a uniform distribution:
I will need to sum the number of PAS in these introns and divide them evenily.
nIntron1.10=sum(pas2intron_intron_grouped_small_withnintron$nBin)
pas2intron_intron_grouped_small_withnintron_enrich=pas2intron_intron_grouped_small_withnintron %>% mutate(nUniform=nIntron1.10/10, UniformNormLength=nUniform/meanSize, UnformlengthandN=UniformNormLength/nGenesum)
Enrichment is the actual normalized number/uniform number:
pas2intron_intron_grouped_small_withnintron_enrich[1,6] / pas2intron_intron_grouped_small_withnintron_enrich[1,9]
[1] 2.688953
Look at just genes with 3 introns.
pas2intron_3introns=pas2intron %>% filter(nintron==3) %>% group_by(Intronid) %>% summarise(nBin=n(), meanSize=mean(intronLength)) %>% mutate(normNBin=nBin/meanSize)
ggplot(pas2intron_3introns,aes(y=normNBin,x=Intronid)) + geom_bar(stat = "identity") + labs(x="Intron in Gene",y="Number introns / average intron length", title="Intron position for genes with 3 introns")
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_1.4.0
loaded via a namespace (and not attached):
[1] Rcpp_1.0.2 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_0.4.0
[17] cli_1.1.0 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_1.3.1 rprojroot_1.3-2
[29] grid_3.5.1 tidyselect_0.2.5 glue_1.3.0 R6_2.3.0
[33] fansi_0.4.0 readxl_1.1.0 rmarkdown_1.10 modelr_0.1.2
[37] magrittr_1.5 whisker_0.3-2 backports_1.1.2 scales_1.0.0
[41] htmltools_0.3.6 rvest_0.3.2 assertthat_0.2.0 colorspace_1.3-2
[45] labeling_0.3 utf8_1.1.4 stringi_1.2.4 lazyeval_0.2.1
[49] munsell_0.5.0 broom_0.5.1 crayon_1.3.4