Last updated: 2018-10-18

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    File Version Author Date Message
    Rmd 38211a8 Peter Carbonetto 2018-10-18 wflow_publish(“chipseq.Rmd”)
    Rmd 90e3ac9 Peter Carbonetto 2018-10-18 wflow_publish(“chipseq.Rmd”)
    Rmd 1ef7492 Peter Carbonetto 2018-10-18 Working on chipseq R Markdown file.

An illustration of “smoothing via adaptive shrinkage” (SMASH) applied to chromatin immunoprecipitation sequencing (“ChIP-seq”) data. This implements the SMASH analysis presented in Sec. 5.2 of the manuscript.

Set up environment

We begin by loading the smashr, ggplot2 and cowplot packages, as well as some additional functions used to implement the analysis below.

source("../code/chipseq.functions.R")
library(smashr)
library(ggplot2)
library(cowplot)
# 
# Attaching package: 'cowplot'
# The following object is masked from 'package:ggplot2':
# 
#     ggsave

Load the ChIP-seq data

The ChIP-seq data are sequencing read counts for transcription factor YY1 in cell line GM12878, restricted to 880,001–1,011,072 bp on chromosome 1. These data were collected as part of the ENCODE (“Encyclopedia Of DNA Elements”) project.

load("../data/reg_880000_1011072.RData")
bppos  <- 880001:1011072
counts <- M[1,] + M[,2]

Note that there are two replicates of the GM12878 cell line, so we analyze the combined read counts from both replicates, stored in the counts vectors.

Run SMASH

Next, we apply SMASH to the read counts to estimate the mean and variance of the underlying signal. It may take several minutes to complete this step.

res <- smash.poiss(counts,post.var = TRUE)

Plot the SMASH estimates

To provide a “baseline” to compare against the SMASH estimates, we retrieve the peaks identified in the same ChIP-seq data using the MACS software.

macs.file <- "../data/Gm1287peaks_chr1_sorted.txt"
peaks <- read.macs.peaks(macs.file,min(bppos),max(bppos))

TO DO: Describe what is being shown in the plot.

create.chipseq.plot(bppos/1e6,counts,res$est,(peaks$start + peaks$end)/2e6,
                    nbreaks = 80) +
  scale_x_continuous(limits = c(0.88,1.02),breaks = seq(0.88,1.02,0.02)) +
  scale_y_continuous(limits = c(-1,9),breaks = seq(0,8,2))

Session information

sessionInfo()
# R version 3.4.3 (2017-11-30)
# Platform: x86_64-apple-darwin15.6.0 (64-bit)
# Running under: macOS High Sierra 10.13.6
# 
# Matrix products: default
# BLAS: /Library/Frameworks/R.framework/Versions/3.4/Resources/lib/libRblas.0.dylib
# LAPACK: /Library/Frameworks/R.framework/Versions/3.4/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] cowplot_0.9.3 ggplot2_3.0.0 smashr_1.2-0 
# 
# loaded via a namespace (and not attached):
#  [1] Rcpp_0.12.19      bindr_0.1.1       pillar_1.2.1     
#  [4] plyr_1.8.4        compiler_3.4.3    git2r_0.23.0     
#  [7] workflowr_1.1.1   R.methodsS3_1.7.1 R.utils_2.6.0    
# [10] bitops_1.0-6      iterators_1.0.9   tools_3.4.3      
# [13] digest_0.6.17     tibble_1.4.2      evaluate_0.11    
# [16] gtable_0.2.0      lattice_0.20-35   pkgconfig_2.0.2  
# [19] rlang_0.2.2       Matrix_1.2-12     foreach_1.4.4    
# [22] yaml_2.2.0        parallel_3.4.3    bindrcpp_0.2.2   
# [25] withr_2.1.2       dplyr_0.7.6       stringr_1.3.1    
# [28] knitr_1.20        REBayes_1.3       caTools_1.17.1   
# [31] tidyselect_0.2.4  rprojroot_1.3-2   grid_3.4.3       
# [34] glue_1.3.0        data.table_1.11.4 R6_2.2.2         
# [37] rmarkdown_1.10    purrr_0.2.5       ashr_2.2-19      
# [40] magrittr_1.5      whisker_0.3-2     backports_1.1.2  
# [43] scales_0.5.0      codetools_0.2-15  htmltools_0.3.6  
# [46] MASS_7.3-48       assertthat_0.2.0  colorspace_1.4-0 
# [49] labeling_0.3      wavethresh_4.6.8  stringi_1.2.4    
# [52] Rmosek_8.0.69     lazyeval_0.2.1    doParallel_1.0.11
# [55] pscl_1.5.2        munsell_0.4.3     truncnorm_1.0-8  
# [58] SQUAREM_2017.10-1 R.oo_1.21.0

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