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# sudo apt-get update | |
# sudo apt-get install git | |
# sudo apt-get build-dep r-base | |
# about 350MB as of R 3.2.0 | |
git clone https://github.com/wch/r-source.git | |
cd r-source | |
R_PAPERSIZE=letter \ | |
R_BATCHSAVE="--no-save --no-restore" \ |
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10228584083 Homo_sapiens/UCSC/hg19/Annotation/Archives/archive-2014-06-02-13-47-56/Variation/snp137.txt | |
12318134451 Homo_sapiens/UCSC/hg19/Annotation/Archives/archive-2014-06-02-13-47-56/Variation/snp138.txt | |
0 Homo_sapiens/UCSC/hg19/ | |
0 Homo_sapiens/UCSC/hg19/Annotation/ | |
0 Homo_sapiens/UCSC/hg19/Annotation/Genes -> Archives/archive-current/Genes | |
0 Homo_sapiens/UCSC/hg19/Annotation/README.txt -> Archives/archive-current/README.txt | |
0 Homo_sapiens/UCSC/hg19/Annotation/SmallRNA -> Archives/archive-current/SmallRNA | |
0 Homo_sapiens/UCSC/hg19/Annotation/Variation -> Archives/archive-current/Variation | |
0 Homo_sapiens/UCSC/hg19/Annotation/Archives/ | |
0 Homo_sapiens/UCSC/hg19/Annotation/Archives/archive-2011-08-30-21-45-18/ |
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If no fasta file is found alongside the other index files, tophat will use the bowtie index you give | |
to build this file and save it to the output directory. This step can take up to an hour for a | |
human-sized genome. | |
############################################################################################################ | |
#!/bin/bash | |
export PATH=$PATH:/opt/RNA-Seq/bin/bowtie2-2.2.1:/opt/RNA-Seq/bin/tophat-2.0.11.Linux_x86_64 | |
export PATH=$PATH:/opt/RNA-Seq/bin/tophat-2.0.11.Linux_x86_64 | |
export PATH=$PATH:/opt/RNA-Seq/bin/samtools-0.1.19/:/opt/RNA-Seq/bin/samtools-0.1.19/bcftools:/opt/RNA-Seq/bin/samtools-0.1.19/misc | |
cd /home/brb/Anders2013 |
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ExpId title reference_ch1 time point_ch2 replicate_ch2 agent_ch2 description | |
GSM561077 F11_FSK2h_rep1 F11 cells, no forskolin 2hrs 1 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561078 F11_FSK2h_rep2 F11 cells, no forskolin 2hrs 2 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561079 F11_FSK2h_rep3 F11 cells, no forskolin 2hrs 3 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561080 F11_FSK4h_rep1 F11 cells, no forskolin 4hrs 1 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561081 F11_FSK4h_rep2 F11 cells, no forskolin 4hrs 2 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561082 F11_FSK4h_rep3 F11 cells, no forskolin 4hrs 3 10µM forskolin gene expression data of regenerating dorsal root ganglion neurons | |
GSM561083 F11_FSK24h_rep1 F11 cells, no forskolin 24hrs 1 10µM forskolin gene expression data of regenerating dorsal r |
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c:\qt\qt-everywhere-5.5.1>configure -release -static -confirm-license -nomake examples -opensource | |
+ cd qtbase | |
+ c:\Qt\qt-everywhere-5.5.1\qtbase\configure.bat -top-level -release -static -confirm-license -nomake examples -opensource | |
Please wait while bootstrapping configure ... | |
<srcbase> = c:/Qt/qt-everywhere-5.5.1/qtbase | |
<outbase> = c:/Qt/qt-everywhere-5.5.1/qtbase | |
jom 1.1.0 - empower your cores | |
cl -c -Yc -nologo -Zc:wchar_t -W3 -GR -EHsc -w34100 -w34189 -DUNICODE -DQT_NO_CODECS -DQT_NO_TEXTCODEC -DQT_NO_UNICODETABLES -DQT_LITE_COMPONENT -DQT_NO_COMPRESS -DQT_NO_THREAD -DQT_NO_QOBJECT -DQT_NO_GEOM_VARIANT -D_CRT_SECURE_NO_DEPRECATE -DQT_BOOTSTRAPPED -DQT_BUILD_CONFIGURE -I"..\..\include" -I"..\..\include\QtCore" -I"..\..\include\QtCore\5.5.1" -I"..\..\include\QtCore\5.5.1\QtCore" -I"c:\Qt\qt-everywhere-5.5.1\qtbase\tools\shared" -I"c:\Qt\qt-everywhere-5.5.1\qtbase\mkspecs\win32-msvc2008" -Fpconfigure_pch.pch -Foconfigure_pch.obj -TP c:\Qt\qt-everywhere-5.5.1\qtbase\tools\configure\configure_pch. |
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x <- read.delim("toy.txt", header=TRUE) | |
summary(x) |
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library(shiny) | |
library(gplots) # Just for redgreen() function. Will be replaced sol. | |
lr2 <- as.matrix(read.delim("toy.txt", header = TRUE)) # 3 genes, 20 arrays, sequential data. | |
sigma <- apply(lr2, 1, sd); sigma <- sigma/max(sigma) | |
# Define server logic required to generate and plot a random distribution | |
shinyServer(function(input, output) { | |
datainput <- reactive(function() { |
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# shiny:::runApp("hello") | |
# | |
# To-Do-List: | |
# missing value case | |
# | |
library(shiny) | |
# library(gplots) # Just for redgreen() function. Will be replaced sol. | |
source(url("http://dl.dropbox.com/u/1014272/heatmapr.r")) | |
source(url("http://dl.dropbox.com/u/1014272/colorpanel.r")) |
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# shiny:::runApp("hello") | |
# | |
# To-Do-List: | |
# missing value case | |
# | |
library(shiny) | |
# library(gplots) # Just for redgreen() function. Will be replaced sol. | |
source(url("http://dl.dropbox.com/u/1014272/heatmapr.r")) | |
source(url("http://dl.dropbox.com/u/1014272/colorpanel.r")) | |
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## Mirrors: uncomment the following and change to your favorite CRAN mirror | |
## if you don't want to use the default (cran.fhcrc.org, Seattle, USA). | |
## options("repos" = "http://cran.fhcrc.org") | |
## Mirrors: uncomment the following and change to your favorite Bioconductor | |
## mirror, if you don't want to use the default (www.bioconductor.org, | |
## Seattle, USA) | |
## options("BioC_mirror" = "http://www.bioconductor.org") | |
local({ |
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