2.1.1 Data

A CSV or R object (rda) file with the clinical information.

2.1.2 Parameters

• Group column: Select the column that identifies the group of each sample.
• Legend text: Text of the legend.
• Title: Title text.
• x-axis limit: Limits the x-axis. If 0, no cut-off is considered.
• Add p-value: Add p-value to the plot.

2.1.3 Size control

Changes the size of the plot

4.1.1 Data

Select a summarized Experiment object (rda)

4.1.2 Parameters control

• Cores: Selects the number of cores to be used in the analysis
• DNA methylation threshold: minimum difference of DNA methylation levels to be considered as hyper/hypomethylated
• P-value adj cut-off: minimum adjusted P-value to be considered as significant.
• Group column: columns with the groups to be used in the analysis
• Groups: Select at least two groups for analysis. For example if it has three groups (g1, g2 and g3) the analysis will output g1 vs g2, g1 vs g3 and g2 vs g3.

4.2.1 Data

Expected input a CSV file with the following pattern:

• For expression: DEA_results_Group_subgruop1_subgroup2_pcut_0.01_logFC.cut_2.csv
• For DNA methylation: DMR_results_Group_subgruop1_subgroup2_pcut_1e-30_meancut_0.55.csv

4.2.2 Volcano options

This box will control the x-axis thresholds “Log FC threshold” for expression and “DNA methylation threshold” for DNA methylation and the y-axis thresholds “P-value adj cut-off”.

4.2.3 Highlighting options

Checkbox option:

• Show names: Shows the names of up/down regulated genes or hypo/hyper methylated probes
• Boxed names: Put names inside a box. To highlight specific genes/probes consider using the “Highlighting option.”

The option “points to highlight” can perform the following functions:

• Highlighted - Shows the names for only the highlighted genes/probes list
• Significant - Shows the names for only the up/down regulated genes or hypo/hyper methylated probes
• Both - Shows both groups

4.2.4 Color control

Change the color of the plot

4.2.5 Size control

Change the size of the plot

4.2.6 Other

• Save file with results: Create a file with the same pattern as the one in the input, but with the new thresholds.

4.3.1 Data

Expected input is an R object (rda) file with a summarized Experiment object.

4.3.2 Parameters control

• Groups column: Select the column that will split the data into groups. This column is selected from the sample matrix (accessed with colData)

• Subgroups column: Select the column that will highlight the different subgroups data in the groups.
• Plot jitters: Show jitters
• Select y limits: Set lower/upper limits for y
• Sort method: Methods to sort the groups in the plot

• x-axis label angle: Change angle of the text in the x-axis

4.3.3 Size control

Change the size of the plot

5.1.1 Gene expression object box

Select a summarized Experiment object (rda)

5.1.2 Normalization of genes

Using the TCGAanalyze_Normalization function you can normalize mRNA transcripts and miRNA, using EDASeq package. This function uses Within-lane normalization procedures to adjust for GC-content effect (or other gene-level effects) on read counts: loess robust local regression, global-scaling, and full-quantile normalization (Risso et al. 2011) and between-lane normalization procedures to adjust for distributional differences between lanes (e.g., sequencing depth): global-scaling and full-quantile normalization (Bullard et al. 2010).

• Normalization of genes?
• Normalization of genes method? Options: gcContent, geneLength

5.1.3 Quantile filter of genes

• Quantile filter of genes?
• DEA test method: quantile, varFilter, filter1, filter2
• Threshold selected as mean for filtering

5.1.4 DEA analysis

• Log FC threshold: Log2FoldChange threshold
• P-value adj cut-off: significant threshold
• Group column: group column in the summarized Experiment object
• Group 1: Group 1 for comparison
• Group 2: Group 2 for comparison
• DEA test method: options glmRT, exactTest

After the analysis is completed, the results will be saved into a CSV file. The Delta column shown in the results is:
δ = |logFC| × |mean(group1) − mean(group2)|
.

5.1.5 Pathway graphs

• DEA result: Select CSV file create by the analysis.
• Pathway ID: plot results in a pathway graphs. See bioconductor Pathview (Luo and Brouwer 2013) package.

Pathway graphs output.

5.2.1 Data

• Select R object (rda) file: Should receive a summarized Experiment object
• Results file: Should receive the output from the DEA or DMR analysis.

DEA result file should have the following pattern: DEA_result_groupCol_group1_group2_pcut_0.05_logFC.cut_0.csv DMR result file should have the following pattern: DMR_results_groupCol_group1_group2_pcut_0.05_meancut_0.3.csv

5.2.2 Genes/Probes selection

• By status: Based on the results file the user can select to see hyper/hypo methylated probes
• Text: The user can write a list of genes separated by “;” , “,” or a new line

5.2.3 Annotation options

• Columns annotation: using the data in the summarized experiment the user can annotate the heatmap.
• Sort by column: The order of the columns can be sorted by one of the selected columns
• Row annotation: Add annotation to rows

5.2.4 Other options

• Scale data: option “none”, “by row”,“column”
• Cluster rows
• Cluster columns
• Show row names
• Show col names

5.2.5 Size control

Change the size of the plot and the number of bars to plot

5.2.6 Sub-menu: Enrichment analysis

To better understand the underlying biological processes, researchers often retrieve a functional profile of a set of genes that might have an important role. This can be done by performing an enrichment analysis.

Given a set of genes that are up-regulated under certain conditions, an enrichment analysis will identify classes of genes or proteins that are over or under-represented using gene set annotations.

Enrichment analysis menu: Main window.

5.2.7 Gene selection

Input a list of genes by:

• Selection: The user can select by hand multiple genes from a list
• Text: the user can write a list of genes separated by “;” , “,” or a new line
• File: select a file (rda, CSV, txt) with a column Gene_symbol or mRNA

5.2.8 Parameter control

• Size of the text
• x upper limit: x-axis upper limit. If 0 no limit is used.
• Number of bar histograms to show: Maximum number of bars to plot

5.2.9 Plot selection

• Plot Biological Process
• Plot Cellular Component
• Plot Molecular Function
• Plot Pathways

5.2.10 Colors control

Change the color of the plot

5.2.11 Size control

Change the size of the plot and the number of bars to plot

5.2.12 Sub-menu: Network inference

Inference of gene regulatory networks. Starting with the set of differentially expressed genes, we infer gene regulatory networks using the following state-of-the art inference algorithms: ARACNE(Margolin, Nemenman, and al 2006), CLR(Faith et al. 2007), MRNET(Meyer et al. 2007) and C3NET(Altay and Emmert-Streib 2010). These methods are based on mutual inference and use different heuristics to infer the edges in the network. These methods have been made available via Bioconductor/CRAN packages (MINET(Meyer, Lafitte, and Bontempi 2008) and c3net(Altay and Emmert-Streib 2010), respectively).

6.1.1 Data

• Select MAF file: Select a MAF file (.rda) with mutation annotation information
• Select annotation file: Select an R object (rda) with the metadata information. Columns labeled “patient” or “bcr_patient_barcode” should exist.
• Annotation columns: Which columns of the annotation file should be visible?
• Annotation position: Location of the annotation (e.g. Top or bottom).

6.1.2 Gene selection

• Selection: The user can select multiple genes from a list
• Text: The user can write a list of genes separated by “;” , “,” or a new line
• File: Select a file (rda, CSV, txt) with a column Gene_symbol or mRNA

6.1.3 Parameters control

• Remove empty columns? If a sample has no mutation, it will be removed from the plot
• Show column names? Show patient barcodes?
• Show barplot annotation on rows? Show right barplot?