README.md

In AbhishekSinha28/tgcapkg: TGCA Data Analysis

tcgaCleaneR

The goal of tcgaCleaneR is to provide a user-friendly R package to help Bioinformaticians with easy access to a tool that can perform Data Wrangling and Data Analysis on TCGA Pan Cancer Dataset. The package contains a subset of the original TCGA Breast Cancer Data collected from TCGA. The package also contains a detailed set of functionalities that allows user to identify and handle unwanted variations in the TCGA datasets.

Installation

You can install the development version of tcgaCleaneR from GitHub with:

# install.packages("devtools")
devtools::install_github("AbhishekSinha28/tcgaCleaneR", ref="master")

TCGA Functionality

This is a quick walk trough of the tcgaCleaneR functionalities. For the detailed information on the Data Wrangling and Data Analysis functions and arguments in tcgaCleaneR package, you can consider looking at the vignette.

At present, TCGA Pan Cancer Datasets supports Cancer Biology for only four Cancer types. These four cancer type (TCGA datasets) are Breast Cancer (BRCA), Lung Cancer (LUAD), Colon Cancer (COAD) and Rectum Cancer (READ). This implies that RUV-III analysis can only be performed for these four cancer types. This is because the RUV-III approach here requires at least one roughly known biologically homogeneous subclass of samples shared across sources of unwanted variation. Similarly, the vector correlation between Biology and PCs can only be viewed for these four Cancer types.

library(tcgaCleaneR)

Data

data("brca.data")

brca.data
#> class: SummarizedExperiment 
#> dim: 100 1196 
#> metadata(0):
#> assays(3): HTseq_counts HTseq_FPKM HTseq_FPKM.UQ
#> rownames(100): TSPAN6 TNMD ... CROT ABCB4
#> rowData names(9): EnsemblGene_ids Gene_symbol ...
#>   NanostringPanCancer_HK sinscorePanCancer_HK
#> colnames(1196): TCGA-A8-A06Z-01A-11R-A00Z-07
#>   TCGA-A8-A08F-01A-11R-A00Z-07 ... TCGA-5T-A9QA-01A-11R-A41B-07
#>   TCGA-BH-A0H9-11A-22R-A466-07
#> colData names(12): Samples Tissues ... CPE Subtypes

Data Wrangling

Gene Filter

filtered.data <- filterGenesByBiotypes(data=brca.data,gene.type=c("protein.coding"))

Removing lowly expressed genes

filtered.data1 <- filterLowExprGenes(data=filtered.data,gene_count = 20,sample_size = 200)

Purity Filter - Filter Samples based on Tumor Purity

filtered.data2 <- filterSamplesByPurity(data= filtered.data1,purity_cutoff= 0.50)

Library Size Filter

Determine Library Size

plotLibSize(data = filtered.data2, plot_type = "Scatterplot")

Filter samples based on library size

filtered.data3 <- filterSamplesByLibSize(data = filtered.data2, ls_cutoff = 17.5)

Data Analysis

Study Design Plot

The idea behind Study Design plot is to present the summarized information about the filtered data set using HeatMaps.

plotStudyOutline(data = filtered.data3)

PCA

Generate PCA

The principal components (in this context also called singular vectors) of the sample × transcript array of log-counts are the linear combinations of the transcript measurements having the largest, second largest, third largest, etc. variation, standardized to be of unit length and orthogonal to the preceding components. Each will give a single value for each sample.

# Is data input for PCA logical
is.logical(filtered.data3)

pca_data <- computePCA(data = filtered.data3, nPcs = 7, is.log = FALSE)

Plot PCA

Once we have the PCs generated using the PCA function the next step is to visualize those PCs with respect to the sample features like Time, Tissue, Plate etc., to identify any unwanted variation by identifying patterns in the plots by feature.

library(ggplot2)
library(cowplot)
pca.plot.data <- plotPC(pca.data = pca_data, data = filtered.data3, group = "Time", plot_type = "DensityPlot", pcs.no = c(1,2,3))

PCs correlation with unwanted variations

library(tidyverse)
corr_data <- plotPCsVar(pca.data = pca_data, data = filtered.data3, type = "purity", nPCs = 7)
corr_data

RUV - III

Pseudo Replicate Pseudo Sample(PRPS) Map

#library(tidyverse)
plotPRPS(data = filtered.data3)

PRPS Generation

sample.info <- as.data.frame(SummarizedExperiment::colData(filtered.data3))
expr.data <- as.matrix(SummarizedExperiment::assay(filtered.data3, 'HTseq_counts')) # gene expression data
sample.info$ls <- colSums(expr.data) # adding library size variable

df9 <- createPRPS(expr.data, sample.info, librarySize = 'ls', batch=c('Year', 'Plates'), biology = 'Subtypes', purity='Purity_singscore',include.ls=T, include.purity=T, minSamplesPerBatchPS = 3, minSamplesForPuirtyPS = 3, 
                 minSamplesForPurityPerBiology = 12, minSamplesForLibrarySizePerBatch = 6,
                 minSamplesForLibrarySizePS = 3)

RUV-III

### data input
library(SummarizedExperiment)
### PRPS values
prps.batch <- df9$ps.batch
colnames(prps.batch) <- unlist(lapply(
  colnames(prps.batch),
  function(x) strsplit(x, '-')[[1]][1]
))
prps.ls <- df9$ps.ls
prps.purity <- df9$ps.purity

raw.data <- as.matrix(SummarizedExperiment::assay(filtered.data3, 'HTseq_counts'))
ruv.data <- cbind(raw.data ,prps.batch ,prps.ls, prps.purity )
ruv.data <- t(log2(ruv.data + 1)) # Taking Log 

### replicate matrix
ruv.rep <- ruv::replicate.matrix(row.names(ruv.data))

gene.annot <-  as.data.frame(SummarizedExperiment::rowData(filtered.data3))

### NCG sets - Select House Keeping Genes
ncg.set <- colnames(ruv.data) %in% gene.annot$Gene_symbol[gene.annot$RNAseq_HK == 'yes']

#library(BiocParallel)
#library(BiocSingular)
df10 <- runRUV_III_PRPS(ruv.data = ruv.data, ruv.rep = ruv.rep, ncg.set = ncg.set, k=1, return.info = TRUE)

Combined Analysis

Combined data

#library(SummarizedExperiment)
gene.annot <-  as.data.frame(SummarizedExperiment::rowData(filtered.data3))

sample.info <-  as.data.frame(SummarizedExperiment::colData(filtered.data3))

ruv.iii.adj <- t(df10$new.ruv.data[1:ncol(raw.data) , ]) # transpose

raw.count <- SummarizedExperiment::assay(filtered.data3, 'HTseq_counts')
raw.count <- log2(raw.count + 1) # Taking Log 
fpkm <- SummarizedExperiment::assay(filtered.data3, 'HTseq_FPKM')
fpkm <- log2(fpkm + 1) # Taking Log 
fpkm.uq <- SummarizedExperiment::assay(filtered.data3, 'HTseq_FPKM.UQ')
fpkm.uq <- log2(fpkm.uq + 1) # Taking Log 
RUV_III <- ruv.iii.adj

combined_data <- SummarizedExperiment(assays = list(HTseq_counts = raw.count, HTseq_FPKM = fpkm,
                                                HTseq_FPKM.UQ = fpkm.uq, RUV_III = RUV_III),
                                  colData = sample.info,
                                  rowData = gene.annot)

combined_data
#> class: SummarizedExperiment 
#> dim: 96 266 
#> metadata(0):
#> assays(4): HTseq_counts HTseq_FPKM HTseq_FPKM.UQ RUV_III
#> rownames(96): TSPAN6 TNMD ... CROT ABCB4
#> rowData names(9): EnsemblGene_ids Gene_symbol ...
#>   NanostringPanCancer_HK sinscorePanCancer_HK
#> colnames(266): TCGA-A8-A06Z-01A-11R-A00Z-07
#>   TCGA-AN-A0AK-01A-21R-A00Z-07 ... TCGA-S3-AA11-01A-31R-A41B-07
#>   TCGA-AC-A4ZE-01A-11R-A41B-07
#> colData names(12): Samples Tissues ... CPE Subtypes

PCA on Combined Data

df11 <- computePCA(data = combined_data, nPcs = 7, is.log = TRUE)

PCs correlation with unwanted variations in Combined Data

df12 <- plotPCsVar(pca.data = df11, data = combined_data, type = "purity", nPCs = 7)
df12

AbhishekSinha28/tgcapkg documentation built on May 3, 2022, 7:40 a.m.