Nothing
## ----style, echo=FALSE, results="asis", message=FALSE-------------------------
knitr::opts_chunk$set(tidy = FALSE,
warning = FALSE,
message = FALSE)
## ----install, eval=FALSE, warning=FALSE---------------------------------------
# if (!require("BiocManager")) {
# install.packages("BiocManager")
# }
# BiocManager::install("RNASeqRData")
## ----fig.width=10, echo=FALSE------------------------------------------------
library(png)
library(grid)
img <- readPNG("figure/whole_file_structure.png")
grid.raster(img, just = "center")
## ----fig.width=10, echo=FALSE-------------------------------------------------
img <- readPNG("figure/input_files_structure.png")
grid.raster(img, just = "center")
## ----fig.width=10, echo=FALSE-------------------------------------------------
img <- readPNG("figure/phenodata_csv.png")
grid.raster(img, just = "center")
## ---- warning=FALSE-----------------------------------------------------------
library(RNASeqR)
library(RNASeqRData)
## -----------------------------------------------------------------------------
input_files.path <- system.file("extdata/", package = "RNASeqRData")
#rnaseq_result.path <- "/Users/chaokuan-hao/Documents/ANU_2019_Semester_2/Lanfear_Lab/HI"
rnaseq_result.path <- "/tmp/RNASeqR/"
dir.create(rnaseq_result.path, recursive = TRUE)
list.files(input_files.path, recursive = TRUE)
## ---- warning=FALSE-----------------------------------------------------------
exp <- RNASeqRParam(path.prefix = rnaseq_result.path,
input.path.prefix = input_files.path,
genome.name = "Saccharomyces_cerevisiae_XV_Ensembl",
sample.pattern = "SRR[0-9]*_XV",
independent.variable = "state",
case.group = "60mins_ID20_amphotericin_B",
control.group = "60mins_ID20_control",
fastq.gz.type = "PE")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# exp <- RNASeqRParam(path.prefix = rnaseq_result.path,
# input.path.prefix = input_files.path,
# genome.name = "Saccharomyces_cerevisiae_XV_Ensembl",
# sample.pattern = "SRR[0-9]*_XV",
# independent.variable = "state",
# case.group = "60mins_ID20_amphotericin_B",
# control.group = "60mins_ID20_control",
# fastq.gz.type = "SE")
## ---- warning=FALSE-----------------------------------------------------------
show(exp)
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqEnvironmentSet_CMD(exp)
## ---- warning=FALSE-----------------------------------------------------------
RNASeqEnvironmentSet(exp)
## ----fig.width=20, echo=FALSE-------------------------------------------------
img <- readPNG("figure/fastqReport.png")
grid.raster(img, just = "center")
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqQualityAssessment_CMD(exp)
## ---- warning=FALSE-----------------------------------------------------------
RNASeqQualityAssessment(exp)
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# Update_Fastq_gz (RNASeqRParam = exp,
# prepared_fastq_gz = paste0(input_files.path,
# "/input_files/raw_fastq.gz/"),
# target_samples = "ALL")
## ----fig.width=6,fig.height=6, echo=FALSE-------------------------------------
img <- readPNG("figure/Alignment_Report/Alignment_Result_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6,fig.height=6, echo=FALSE-------------------------------------
img <- readPNG("figure/Alignment_Report/Overall_Mapping_rate_ggplot2.png")
grid.raster(img, just = "center")
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqReadProcess_CMD(exp)
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqReadProcess_CMD(exp, STAR.Alignment.run=TRUE,
# Hisat2.Index.run=FALSE,
# Hisat2.Alignment.run = FALSE)
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# RNASeqReadProcess(exp)
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqReadProcess(exp, STAR.Alignment.run=TRUE,
# Hisat2.Index.run=FALSE,
# Hisat2.Alignment.run = FALSE)
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/Statistical_Results.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Frequency/Frequency_Plot_normalized_count_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Frequency/Frequency_Plot_log_normalized_count_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Distribution/Box_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Distribution/Violin_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/PCA/Dimension_PCA_Plot_factoextra.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/PCA/PCA_Plot_factoextra.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/PCA/PCA_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Correlation/Correlation_Heat_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Correlation/Correlation_Dot_Plot_corrplot.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Correlation/Correlation_Bar_Plot_PerformanceAnalytics.png")
grid.raster(img, just = "center")
## ----fig.width=8, fig.height=8, echo=FALSE------------------------------------
img <- readPNG("figure/DE/Volcano_Plot_graphics.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/PCA/Dimension_PCA_Plot_factoextra.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/PCA/PCA_Plot_factoextra.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/PCA/PCA_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/Heatmap_Plot_pheatmap.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/transcript_related/Distribution_Transcript_Count_per_Gene_Plot.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/transcript_related/Distribution_Transcript_Length_Plot.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/ballgown_MA_Plot_ggplot2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/preDE/Dispersion_Plot_DESeq2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/DE/MA_Plot_DESeq2.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/edgeR_MeanVar_Plot_edgeR.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/edgeR_BCV_Plot_edgeR.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/edgeR_MDS_Plot_edgeR.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/edgeR_Smear_Plot_edgeR.png")
grid.raster(img, just = "center")
## ---- eval=FALSE--------------------------------------------------------------
# RNASeqDifferentialAnalysis_CMD(exp)
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# RNASeqDifferentialAnalysis(exp)
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/GO_analysis/GO_CC_Classification_Bar_Plot_clusterProfiler.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/GO_analysis/GO_MF_Overrepresentation_Bar_Plot_clusterProfiler.png")
grid.raster(img, just = "center")
## ----fig.width=6, height=6, echo=FALSE----------------------------------------
img <- readPNG("figure/GO_analysis/GO_MF_Overrepresentation_Dot_Plot_clusterProfiler.png")
grid.raster(img, just = "center")
## ---- eval = FALSE------------------------------------------------------------
# RNASeqGoKegg_CMD(exp,
# OrgDb.species = "org.Sc.sgd.db",
# go.level = 3,
# input.TYPE.ID = "GENENAME",
# KEGG.organism = "sce")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# RNASeqGoKegg(exp,
# OrgDb.species = "org.Sc.sgd.db",
# go.level = 3,
# input.TYPE.ID = "GENENAME",
# KEGG.organism = "sce")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# exp_Sam <- RNASeqRParam_Sam(path.prefix = rnaseq_result.path,
# input.path.prefix = input_files.path,
# genome.name = "Saccharomyces_cerevisiae_XV_Ensembl",
# sample.pattern = "SRR[0-9]*_XV",
# independent.variable = "state",
# case.group = "60mins_ID20_amphotericin_B",
# control.group = "60mins_ID20_control")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# exp_Bam <- RNASeqRParam_Bam(path.prefix = rnaseq_result.path,
# input.path.prefix = input_files.path,
# genome.name = "Saccharomyces_cerevisiae_XV_Ensembl",
# sample.pattern = "SRR[0-9]*_XV",
# independent.variable = "state",
# case.group = "60mins_ID20_amphotericin_B",
# control.group = "60mins_ID20_control")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# exp <- RNASeqRParam(path.prefix = rnaseq_result.path,
# input.path.prefix = input_files.path,
# genome.name = "Saccharomyces_cerevisiae_XV_Ensembl",
# sample.pattern = "SRR[0-9]*_XV",
# independent.variable = "state",
# case.group = "60mins_ID20_amphotericin_B",
# control.group = "60mins_ID20_control",
# fastq.gz.type = "PE")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# RNASeqEnvironmentSet(exp)
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# All_Steps_Interface_CMD(exp,
# OrgDb.species = "org.Sc.sgd.db",
# go.level = 3,
# input.TYPE.ID = "GENENAME",
# KEGG.organism = "sce")
## ---- warning=FALSE, eval=FALSE-----------------------------------------------
# All_Steps_Interface(exp,
# OrgDb.species = "org.Sc.sgd.db",
# go.level = 3,
# input.TYPE.ID = "GENENAME",
# KEGG.organism = "sce")
## -----------------------------------------------------------------------------
sessionInfo()
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