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<title>Create Gviz genome track plots</title>

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<h1 class="title toc-ignore">Create Gviz genome track plots</h1>
<h4 class="author"><em>Briana Mittleman</em></h4>
<h4 class="date"><em>2017-12-13</em></h4>

</div>


<!-- The file analysis/chunks.R contains chunks that define default settings
shared across the workflowr files. -->
<!-- Update knitr chunk options -->
<!-- Insert the date the file was last updated -->
<p><strong>Last updated:</strong> 2017-12-19</p>
<!-- Insert the code version (Git commit SHA1) if Git repository exists and R
 package git2r is installed -->
<p><strong>Code version:</strong> 1d63e1d</p>
<!-- Add your analysis here -->
<p>The goal of this analysis is to create nice plots showing that we are getting as much information as the 1 lane from the Mayer sample. I will do this with our merged data vs. their 1 lane.</p>
<p>Genes from IGV that I want to use:</p>
<ul>
<li><p>HERPUD1 chr16:56,964,002-56,979,793</p></li>
<li><p>ACTB chr7:5,564,779-5,572,232</p></li>
<li><p>CCNB2 chr15:59,396,707-59,401,006</p></li>
<li><p>chr11:234,336-239,997</p></li>
<li><p>KIAA0100 chr17:26,968,078-26,974,887</p></li>
<li><p>HECTD1 chr14:31,672,040-31,681,043</p></li>
<li><p>STAG1 chr3:136,469,421-136,472,771</p></li>
<li><p>SRSF3</p></li>
<li><p>ENO1</p></li>
</ul>
<p>Load Packages:</p>
<pre class="r"><code>library(Gviz)</code></pre>
<pre><code>Loading required package: S4Vectors</code></pre>
<pre><code>Loading required package: stats4</code></pre>
<pre><code>Loading required package: BiocGenerics</code></pre>
<pre><code>Loading required package: parallel</code></pre>
<pre><code>
Attaching package: &#39;BiocGenerics&#39;</code></pre>
<pre><code>The following objects are masked from &#39;package:parallel&#39;:

    clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
    clusterExport, clusterMap, parApply, parCapply, parLapply,
    parLapplyLB, parRapply, parSapply, parSapplyLB</code></pre>
<pre><code>The following objects are masked from &#39;package:stats&#39;:

    IQR, mad, sd, var, xtabs</code></pre>
<pre><code>The following objects are masked from &#39;package:base&#39;:

    anyDuplicated, append, as.data.frame, cbind, colMeans,
    colnames, colSums, do.call, duplicated, eval, evalq, Filter,
    Find, get, grep, grepl, intersect, is.unsorted, lapply,
    lengths, Map, mapply, match, mget, order, paste, pmax,
    pmax.int, pmin, pmin.int, Position, rank, rbind, Reduce,
    rowMeans, rownames, rowSums, sapply, setdiff, sort, table,
    tapply, union, unique, unsplit, which, which.max, which.min</code></pre>
<pre><code>
Attaching package: &#39;S4Vectors&#39;</code></pre>
<pre><code>The following object is masked from &#39;package:base&#39;:

    expand.grid</code></pre>
<pre><code>Loading required package: IRanges</code></pre>
<pre><code>Loading required package: GenomicRanges</code></pre>
<pre><code>Loading required package: GenomeInfoDb</code></pre>
<pre><code>Loading required package: grid</code></pre>
<pre class="r"><code>library(GenomicRanges)
library(biomaRt)
library(TxDb.Hsapiens.UCSC.hg19.knownGene)</code></pre>
<pre><code>Loading required package: GenomicFeatures</code></pre>
<pre><code>Loading required package: AnnotationDbi</code></pre>
<pre><code>Loading required package: Biobase</code></pre>
<pre><code>Welcome to Bioconductor

    Vignettes contain introductory material; view with
    &#39;browseVignettes()&#39;. To cite Bioconductor, see
    &#39;citation(&quot;Biobase&quot;)&#39;, and for packages &#39;citation(&quot;pkgname&quot;)&#39;.</code></pre>
<pre class="r"><code>library(&quot;IRanges&quot;)
library(&quot;dplyr&quot;)</code></pre>
<pre><code>
Attaching package: &#39;dplyr&#39;</code></pre>
<pre><code>The following object is masked from &#39;package:AnnotationDbi&#39;:

    select</code></pre>
<pre><code>The following object is masked from &#39;package:Biobase&#39;:

    combine</code></pre>
<pre><code>The following object is masked from &#39;package:biomaRt&#39;:

    select</code></pre>
<pre><code>The following objects are masked from &#39;package:GenomicRanges&#39;:

    intersect, setdiff, union</code></pre>
<pre><code>The following object is masked from &#39;package:GenomeInfoDb&#39;:

    intersect</code></pre>
<pre><code>The following objects are masked from &#39;package:IRanges&#39;:

    collapse, desc, intersect, setdiff, slice, union</code></pre>
<pre><code>The following objects are masked from &#39;package:S4Vectors&#39;:

    first, intersect, rename, setdiff, setequal, union</code></pre>
<pre><code>The following objects are masked from &#39;package:BiocGenerics&#39;:

    combine, intersect, setdiff, union</code></pre>
<pre><code>The following objects are masked from &#39;package:stats&#39;:

    filter, lag</code></pre>
<pre><code>The following objects are masked from &#39;package:base&#39;:

    intersect, setdiff, setequal, union</code></pre>
<pre class="r"><code>library(&quot;data.table&quot;)</code></pre>
<pre><code>
Attaching package: &#39;data.table&#39;</code></pre>
<pre><code>The following objects are masked from &#39;package:dplyr&#39;:

    between, first, last</code></pre>
<pre><code>The following object is masked from &#39;package:GenomicRanges&#39;:

    shift</code></pre>
<pre><code>The following object is masked from &#39;package:IRanges&#39;:

    shift</code></pre>
<pre><code>The following objects are masked from &#39;package:S4Vectors&#39;:

    first, second</code></pre>
<pre class="r"><code>library(&quot;GenomicAlignments&quot;)</code></pre>
<pre><code>Loading required package: SummarizedExperiment</code></pre>
<pre><code>Loading required package: DelayedArray</code></pre>
<pre><code>Loading required package: matrixStats</code></pre>
<pre><code>
Attaching package: &#39;matrixStats&#39;</code></pre>
<pre><code>The following object is masked from &#39;package:dplyr&#39;:

    count</code></pre>
<pre><code>The following objects are masked from &#39;package:Biobase&#39;:

    anyMissing, rowMedians</code></pre>
<pre><code>
Attaching package: &#39;DelayedArray&#39;</code></pre>
<pre><code>The following objects are masked from &#39;package:matrixStats&#39;:

    colMaxs, colMins, colRanges, rowMaxs, rowMins, rowRanges</code></pre>
<pre><code>The following object is masked from &#39;package:base&#39;:

    apply</code></pre>
<pre><code>Loading required package: Biostrings</code></pre>
<pre><code>Loading required package: XVector</code></pre>
<pre><code>
Attaching package: &#39;Biostrings&#39;</code></pre>
<pre><code>The following object is masked from &#39;package:DelayedArray&#39;:

    type</code></pre>
<pre><code>The following object is masked from &#39;package:base&#39;:

    strsplit</code></pre>
<pre><code>Loading required package: Rsamtools</code></pre>
<pre><code>
Attaching package: &#39;GenomicAlignments&#39;</code></pre>
<pre><code>The following object is masked from &#39;package:data.table&#39;:

    last</code></pre>
<pre><code>The following object is masked from &#39;package:dplyr&#39;:

    last</code></pre>
<p>Upload data:</p>
<pre class="r"><code>chr= &quot;chr7&quot;
gen= &quot;hg19&quot;

merged_data_7= DataTrack(range = &quot;../data/bam_files_chr/merged_Net1_chr.bam&quot;, genome = gen, type = &quot;h&quot;, name = &quot;Merged&quot;, window = -1, chromosome = &quot;chr7&quot;)
mayer_data_7= DataTrack(range = &quot;../data/bam_files_chr/mayer_chr.bam&quot;, genome = gen, type = &quot;h&quot;, name = &quot;Mayer&quot;, window = -1, chromosome = &quot;chr7&quot;)



refGenes &lt;- UcscTrack(genome= gen, chromosome=chr, 
     track=&quot;RefSeq Genes&quot;, from = 5555158, to = 5581854, 
     trackType=&quot;GeneRegionTrack&quot;, rstarts=&quot;exonStarts&quot;, 
     rends=&quot;exonEnds&quot;, gene=&quot;name&quot;, symbol=&quot;name2&quot;, 
     transcript=&quot;name&quot;, strand=&quot;strand&quot;, fill=&quot;#800000&quot;, name=&quot;RefSeq Genes&quot;, showId=TRUE)
gtrack = GenomeAxisTrack()


itrack= IdeogramTrack(genome = gen, chromosome = chr)


#plots
plotTracks(list(itrack,gtrack, merged_data_7, mayer_data_7, refGenes), from = 5555158, to = 5581854,  background.title=&quot;darkblue&quot;,  background.panel = &quot;#FFFEDB&quot;)</code></pre>
<p><img src="figure/gviz_plots.Rmd/unnamed-chunk-2-1.png" width="672" style="display: block; margin: auto;" /></p>
<pre class="r"><code>merged_anno_7= AnnotationTrack(range = &quot;../data/bam_files_chr/merged_Net1_chr.bam&quot;, genome = gen, name = &quot;Merged&quot;, window = -1, chromosome = chr)
mayer_anno_7= AnnotationTrack(range = &quot;../data/bam_files_chr/mayer_chr.bam&quot;, genome = gen, name = &quot;Mayer&quot;, window = -1, chromosome = chr)
plotTracks(list(merged_data_7, merged_anno_7), from = 5564779, to = 5572232)</code></pre>
<p><img src="figure/gviz_plots.Rmd/unnamed-chunk-3-1.png" width="672" style="display: block; margin: auto;" /></p>
<pre class="r"><code>plotTracks(list(mayer_data_7,mayer_anno_7), from = 5564779, to = 5572232)</code></pre>
<p><img src="figure/gviz_plots.Rmd/unnamed-chunk-3-2.png" width="672" style="display: block; margin: auto;" /></p>
<div id="create-a-function-for-the-plots" class="section level3">
<h3>Create a function for the plots</h3>
<pre class="r"><code>track_plot=function(chrom, from, to){
  gen= &quot;hg19&quot;
  chr= chrom
  merged_data= DataTrack(range = &quot;../data/bam_files_chr/merged_Net1_chr.bam&quot;, genome = gen, type = &quot;h&quot;, name = &quot;Merged&quot;, window = -1, chromosome = chr)
  mayer_data= DataTrack(range = &quot;../data/bam_files_chr/mayer_chr.bam&quot;, genome = gen, type = &quot;h&quot;, name = &quot;Mayer&quot;, window = -1, chromosome = chr)
  refGenes &lt;- UcscTrack(genome= gen, chromosome=chr, 
     track=&quot;RefSeq Genes&quot;, from = from, to = to, 
     trackType=&quot;GeneRegionTrack&quot;, rstarts=&quot;exonStarts&quot;, 
     rends=&quot;exonEnds&quot;, gene=&quot;name&quot;, symbol=&quot;name2&quot;, 
     transcript=&quot;name&quot;, strand=&quot;strand&quot;, fill=&quot;#800000&quot;, name=&quot;RefSeq Genes&quot;, showId=TRUE)
  gtrack = GenomeAxisTrack()
  itrack= IdeogramTrack(genome = gen, chromosome = chr)
  plot= plotTracks(list(itrack,gtrack, merged_data, mayer_data, refGenes), from = from, to = to,  background.title=&quot;darkblue&quot;,  background.panel = &quot;#FFFEDB&quot;)
  return(plot)
}</code></pre>
<pre class="r"><code>#plot_SRSF3= track_plot(&quot;chr6&quot;,36564332,36571507)</code></pre>
<pre class="r"><code>#plot_ENO1=track_plot(&quot;chr1&quot;,8919652,8940558 )</code></pre>
<pre class="r"><code>#plot_tars=track_plot(&quot;chr5&quot;,33438802,33468000)</code></pre>
<pre class="r"><code>#plot_CAXN= track_plot(&quot;chr5&quot;,179123129,179159838)
#future: change track size with sizes=c(5,1,5) commpand in plot track
#plot_ALDOA= track_plot(&quot;chr16&quot;,30080421,30082314)
  
#plot_XRCC5= track_plot(&quot;chr2&quot;, 216968869,217009667)

#plot_TUBB= track_plot(&quot;chr6&quot;,30684274,30698626)</code></pre>
<div id="fix-in-terminal" class="section level4">
<h4>Fix in terminal</h4>
<p>Add the chr tag to the bam files.</p>
<pre class="bash"><code>samtools view -h SRR1575922-sort.bam | awk &#39;BEGIN{FS=OFS=&quot;\t&quot;} (/^@/ &amp;&amp; !/@SQ/){print $0} $2~/^SN:[1-9]|^SN:X|^SN:Y|^SN:MT/{print $0}  $3~/^[1-9]|X|Y|MT/{$3=&quot;chr&quot;$3; print $0} &#39; | sed &#39;s/SN:/SN:chr/g&#39; | sed &#39;s/chrMT/chrM/g&#39; | samtools view -bS - &gt; mayer_chr.bam

samtools view -h merged_Net1.bam | awk &#39;BEGIN{FS=OFS=&quot;\t&quot;} (/^@/ &amp;&amp; !/@SQ/){print $0} $2~/^SN:[1-9]|^SN:X|^SN:Y|^SN:MT/{print $0}  $3~/^[1-9]|X|Y|MT/{$3=&quot;chr&quot;$3; print $0} &#39; | sed &#39;s/SN:/SN:chr/g&#39; | sed &#39;s/chrMT/chrM/g&#39; | samtools view -bS - &gt; merged_Net1_chr.bam</code></pre>
<p>index the bam files:</p>
<pre class="bash"><code>samtools index mayer_chr.bam
samtools index merged_Net1_chr.bam</code></pre>
</div>
</div>
<div id="session-information" class="section level2">
<h2>Session information</h2>
<!-- Insert the session information into the document -->
<pre class="r"><code>sessionInfo()</code></pre>
<pre><code>R version 3.4.2 (2017-09-28)
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/3.4/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] grid      parallel  stats4    stats     graphics  grDevices utils    
 [8] datasets  methods   base     

other attached packages:
 [1] GenomicAlignments_1.14.1               
 [2] Rsamtools_1.30.0                       
 [3] Biostrings_2.46.0                      
 [4] XVector_0.18.0                         
 [5] SummarizedExperiment_1.8.0             
 [6] DelayedArray_0.4.1                     
 [7] matrixStats_0.52.2                     
 [8] data.table_1.10.4-3                    
 [9] dplyr_0.7.4                            
[10] TxDb.Hsapiens.UCSC.hg19.knownGene_3.2.2
[11] GenomicFeatures_1.30.0                 
[12] AnnotationDbi_1.40.0                   
[13] Biobase_2.38.0                         
[14] biomaRt_2.34.0                         
[15] Gviz_1.22.2                            
[16] GenomicRanges_1.30.0                   
[17] GenomeInfoDb_1.14.0                    
[18] IRanges_2.12.0                         
[19] S4Vectors_0.16.0                       
[20] BiocGenerics_0.24.0                    

loaded via a namespace (and not attached):
 [1] ProtGenerics_1.10.0           bitops_1.0-6                 
 [3] bit64_0.9-7                   RColorBrewer_1.1-2           
 [5] progress_1.1.2                httr_1.3.1                   
 [7] rprojroot_1.2                 tools_3.4.2                  
 [9] backports_1.1.2               R6_2.2.2                     
[11] rpart_4.1-11                  Hmisc_4.0-3                  
[13] DBI_0.7                       lazyeval_0.2.1               
[15] colorspace_1.3-2              nnet_7.3-12                  
[17] gridExtra_2.3                 prettyunits_1.0.2            
[19] RMySQL_0.10.13                bit_1.1-12                   
[21] curl_3.1                      compiler_3.4.2               
[23] git2r_0.19.0                  htmlTable_1.11.0             
[25] rtracklayer_1.38.2            scales_0.5.0                 
[27] checkmate_1.8.5               stringr_1.2.0                
[29] digest_0.6.13                 foreign_0.8-69               
[31] rmarkdown_1.8                 base64enc_0.1-3              
[33] dichromat_2.0-0               pkgconfig_2.0.1              
[35] htmltools_0.3.6               ensembldb_2.2.0              
[37] BSgenome_1.46.0               htmlwidgets_0.9              
[39] rlang_0.1.4                   rstudioapi_0.7               
[41] RSQLite_2.0                   BiocInstaller_1.28.0         
[43] shiny_1.0.5                   bindr_0.1                    
[45] BiocParallel_1.12.0           acepack_1.4.1                
[47] VariantAnnotation_1.24.2      RCurl_1.95-4.8               
[49] magrittr_1.5                  GenomeInfoDbData_0.99.1      
[51] Formula_1.2-2                 Matrix_1.2-12                
[53] Rcpp_0.12.14                  munsell_0.4.3                
[55] stringi_1.1.6                 yaml_2.1.16                  
[57] zlibbioc_1.24.0               plyr_1.8.4                   
[59] AnnotationHub_2.10.1          blob_1.1.0                   
[61] lattice_0.20-35               splines_3.4.2                
[63] knitr_1.17                    XML_3.98-1.9                 
[65] glue_1.2.0                    evaluate_0.10.1              
[67] biovizBase_1.26.0             latticeExtra_0.6-28          
[69] httpuv_1.3.5                  gtable_0.2.0                 
[71] purrr_0.2.4                   tidyr_0.7.2                  
[73] assertthat_0.2.0              ggplot2_2.2.1                
[75] mime_0.5                      xtable_1.8-2                 
[77] AnnotationFilter_1.2.0        survival_2.41-3              
[79] tibble_1.3.4                  memoise_1.1.0                
[81] bindrcpp_0.2                  cluster_2.0.6                
[83] interactiveDisplayBase_1.16.0</code></pre>
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