Peak To Gene Assignment

Last updated: 2018-09-26

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Ignored files:
    Ignored:    .DS_Store
    Ignored:    .Rhistory
    Ignored:    .Rproj.user/
    Ignored:    output/.DS_Store

Untracked files:
    Untracked:  analysis/ncbiRefSeq_sm.sort.mRNA.bed
    Untracked:  analysis/snake.config.notes.Rmd
    Untracked:  analysis/verifyBAM.Rmd
    Untracked:  data/18486.genecov.txt
    Untracked:  data/APApeaksYL.total.inbrain.bed
    Untracked:  data/NuclearApaQTLs.txt
    Untracked:  data/RNAkalisto/
    Untracked:  data/TotalApaQTLs.txt
    Untracked:  data/Totalpeaks_filtered_clean.bed
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    Untracked:  data/combined_reads_mapped_three_prime_seq.csv
    Untracked:  data/filtered_APApeaks_merged_allchrom_refseqTrans.closest2End.bed
    Untracked:  data/filtered_APApeaks_merged_allchrom_refseqTrans.closest2End.noties.bed
    Untracked:  data/gencov.test.csv
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Unstaged changes:
    Modified:   analysis/28ind.peak.explore.Rmd
    Modified:   analysis/callMolQTLS.Rmd
    Modified:   analysis/cleanupdtseq.internalpriming.Rmd
    Modified:   analysis/dif.iso.usage.leafcutter.Rmd
    Modified:   analysis/diff_iso_pipeline.Rmd
    Modified:   analysis/explore.filters.Rmd
    Modified:   analysis/overlap_qtls.Rmd
    Modified:   analysis/peakOverlap_oppstrand.Rmd
    Modified:   analysis/pheno.leaf.comb.Rmd
    Modified:   analysis/test.max2.Rmd
    Modified:   code/Snakefile

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.

Expand here to see past versions:

File	Version	Author	Date	Message
Rmd	dd2b07d	Briana Mittleman	2018-09-26	account for ties
html	149d033	Briana Mittleman	2018-09-26	Build site.
html	aaed5fd	Briana Mittleman	2018-09-26	Build site.
Rmd	eda266e	Briana Mittleman	2018-09-26	test peak to gene transcript dist

library(tidyverse)

── Attaching packages ──────────────────────────────────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──

✔ ggplot2 3.0.0     ✔ purrr   0.2.5
✔ tibble  1.4.2     ✔ dplyr   0.7.6
✔ tidyr   0.8.1     ✔ stringr 1.3.1
✔ readr   1.1.1     ✔ forcats 0.3.0

── Conflicts ─────────────────────────────────────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag()    masks stats::lag()

library(workflowr)

This is workflowr version 1.1.1
Run ?workflowr for help getting started

I will use this analysis to investigate further the best way to assign the peaks to a gene. Right now I am using

Prepare referece

#!/bin/bash

#SBATCH --job-name=intGenes_combfilterPeaksOppStrand
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=intGenes_combfilterPeaksOppStrand.out
#SBATCH --error=intGenes_combfilterPeaksOppStrand.err
#SBATCH --partition=broadwl
#SBATCH --mem=12G
#SBATCH --mail-type=END

module load Anaconda3
source activate three-prime-env

bedtools intersect -wa -wb -sorted -S -a /project2/gilad/briana/threeprimeseq/data/mergedPeaks_comb/filtered_APApeaks_merged_allchrom.named.fixed.bed -b /project2/gilad/briana/genome_anotation_data/ncbiRefSeq_sm_noChr.sort.mRNA.bed > /project2/gilad/briana/threeprimeseq/data/mergedPeaks_comb/filtered_APApeaks_merged_allchrom_refseqGenes.OppStrand.bed

This results in peaks being mapped to multiple genes. I want to use a method where I look for the closest end of transcript to each peak then use that gene for the assignment. This would mean each peak is assigned to one gene.

Create a python script to process the NCBI file. I want protien coding transcript ends with the associated gene names. Original file: ncbiRefSeq.txt

Column 2 transcript name
Column 13 gene name
NM is protein coding

EndOfProCodTrans.py

def main(inF, outF):
  infile= open(inF, "r")
  fout = open(outF,'w')
  for line in infile:
      linelist=line.split()
      transcript=linelist[1]
      transcript_id=transcript.split("_")[0]
      if transcript_id=="NM":
          chr=linelist[2][3:]
          strand=linelist[3] 
          gene= linelist[12]
          if strand == "+" :
              end = int(linelist[7])
              end2= end - 1
              fout.write("%s\t%d\t%d\t%s:%s\t.\t%s\n"%(chr, end2, end, transcript,gene, strand))
          if strand == "-":
              end= int(linelist[4])
              end2= end + 1
              fout.write("%s\t%d\t%d\t%s:%s\t.\t%s\n"%(chr, end, end2, transcript,gene, strand))


if __name__ == "__main__":
    inF = "/project2/gilad/briana/genome_anotation_data/ncbiRefSeq.txt"
    outF= "/project2/gilad/briana/genome_anotation_data/ncbiRefSeq_endProtCodGenes.txt"
    main(inF, outF)

Find closest gene to each peak

bedtools closest

-A peaks /project2/gilad/briana/threeprimeseq/data/mergedPeaks_comb/filtered_APApeaks_merged_allchrom.named.fixed.bed -B transcript file /project2/gilad/briana/genome_anotation_data/ncbiRefSeq_endProtCodGenes_sort.txt -S (opposite strand) -D b (give distance wrt to gene strand)


#!/bin/bash

#SBATCH --job-name=TransClosest2End
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=TransClosest2End.out
#SBATCH --error=TransClosest2End.err
#SBATCH --partition=broadwl
#SBATCH --mem=12G
#SBATCH --mail-type=END

module load Anaconda3 

source activate three-prime-env


bedtools closest -S -D b -a /project2/gilad/briana/threeprimeseq/data/mergedPeaks_comb/filtered_APApeaks_merged_allchrom.named.fixed.bed -b  /project2/gilad/briana/genome_anotation_data/ncbiRefSeq_endProtCodGenes_sort.txt > /project2/gilad/briana/threeprimeseq/data/mergedPeaks_comb/filtered_APApeaks_merged_allchrom_refseqTrans.closest2End.bed

I will take a look at this file in R then I will process the file in python.

names=c("PeakChr", "PeakStart", "PeakEnd", "PeakName","PeakScore", "PeakStrand", "GeneChr", "GeneStart", "GeneEnd", "Transcript", "GeneScore", "GeneStrand", "Distance" )
peak2transDist=read.table("../data/filtered_APApeaks_merged_allchrom_refseqTrans.closest2End.bed", col.names = names, stringsAsFactors = F, header=F)

ggplot(peak2transDist, aes(x=abs(Distance)))+ geom_density() + scale_x_log10()

Warning: Transformation introduced infinite values in continuous x-axis

Warning: Removed 4362 rows containing non-finite values (stat_density).

Expand here to see past versions of unnamed-chunk-6-1.png:

Version	Author	Date
aaed5fd	Briana Mittleman	2018-09-26

peak2transDist0=peak2transDist %>% filter(Distance==0)
nrow(peak2transDist0)

[1] 4362

peak2transDist200=peak2transDist %>% filter(abs(Distance)<200)
nrow(peak2transDist200)

[1] 23778

summary(peak2transDist$Distance)

    Min.  1st Qu.   Median     Mean  3rd Qu.     Max. 
-5523243   -57698   -12830   -23711     3373  5592124

try adding the no ties flag -t first.

peak2transDist_noties=read.table("../data/filtered_APApeaks_merged_allchrom_refseqTrans.closest2End.noties.bed", col.names = names, stringsAsFactors = F, header=F)
ggplot(peak2transDist_noties, aes(x=abs(Distance)))+ geom_density() + scale_x_log10()

Warning: Transformation introduced infinite values in continuous x-axis

Warning: Removed 2044 rows containing non-finite values (stat_density).

peak2transDist0_noT=peak2transDist_noties%>% filter(Distance==0)
nrow(peak2transDist0_noT)

[1] 2044

peak2transDist200_noT=peak2transDist_noties %>% filter(abs(Distance)<200)
nrow(peak2transDist200_noT)

[1] 10488

summary(peak2transDist$Distance)

    Min.  1st Qu.   Median     Mean  3rd Qu.     Max. 
-5523243   -57698   -12830   -23711     3373  5592124

ggplot(peak2transDist_noties, aes(x=abs(Distance)))+ geom_histogram(binwidth = .5) + scale_x_log10()

Warning: Transformation introduced infinite values in continuous x-axis

Warning: Removed 2044 rows containing non-finite values (stat_bin).

Session information

sessionInfo()

R version 3.5.1 (2018-07-02)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS Sierra 10.12.6

Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/3.5/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/3.5/Resources/lib/libRlapack.dylib

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base     

other attached packages:
 [1] bindrcpp_0.2.2  workflowr_1.1.1 forcats_0.3.0   stringr_1.3.1  
 [5] dplyr_0.7.6     purrr_0.2.5     readr_1.1.1     tidyr_0.8.1    
 [9] tibble_1.4.2    ggplot2_3.0.0   tidyverse_1.2.1

loaded via a namespace (and not attached):
 [1] tidyselect_0.2.4  haven_1.1.2       lattice_0.20-35  
 [4] colorspace_1.3-2  htmltools_0.3.6   yaml_2.2.0       
 [7] rlang_0.2.2       R.oo_1.22.0       pillar_1.3.0     
[10] glue_1.3.0        withr_2.1.2       R.utils_2.7.0    
[13] modelr_0.1.2      readxl_1.1.0      bindr_0.1.1      
[16] plyr_1.8.4        munsell_0.5.0     gtable_0.2.0     
[19] cellranger_1.1.0  rvest_0.3.2       R.methodsS3_1.7.1
[22] evaluate_0.11     labeling_0.3      knitr_1.20       
[25] broom_0.5.0       Rcpp_0.12.18      scales_1.0.0     
[28] backports_1.1.2   jsonlite_1.5      hms_0.4.2        
[31] digest_0.6.16     stringi_1.2.4     grid_3.5.1       
[34] rprojroot_1.3-2   cli_1.0.0         tools_3.5.1      
[37] magrittr_1.5      lazyeval_0.2.1    crayon_1.3.4     
[40] whisker_0.3-2     pkgconfig_2.0.2   xml2_1.2.0       
[43] lubridate_1.7.4   assertthat_0.2.0  rmarkdown_1.10   
[46] httr_1.3.1        rstudioapi_0.7    R6_2.2.2         
[49] nlme_3.1-137      git2r_0.23.0      compiler_3.5.1

This reproducible R Markdown analysis was created with workflowr 1.1.1

Peak To Gene Assignment

Briana Mittleman

9/26/2018

Prepare referece

Find closest gene to each peak

Session information