Get the development version from github:
if(!requireNamespace("devtools", quietly = TRUE))
install.packages("devtools")
devtools::install_github("huerqiang/GeoTcgaData")Or the released version from CRAN:
install.packages("GeoTcgaData")GEO and TCGA provide us with a wealth of data, such as RNA-seq, DNA Methylation, and Copy number variation data. It’s easy to download data from TCGA using the gdc tool, but processing these data into a format suitable for bioinformatics analysis requires more work. This R package was developed to handle these data.
library(GeoTcgaData)
#> Hello, friend! welcome to use!This is a basic example which shows you how to solve a common problem:
The function classify_sample and diff_gene could get the differentially expressioned genes using DESeq2 package. For examples:
library(DESeq2)
profile2 <- classify_sample(kegg_liver)
jieguo <- diff_gene(profile2)The parameter kegg_liver is a matrix or data.frame of gene expression data(count) in TCGA.
The function Merge_methy_tcga could Merge methylation data downloaded from TCGA. This makes it easier to extract differentially methylated genes in the downstream analysis. For example:
dirr = system.file(file.path("extdata","methy"),package="GeoTcgaData")
merge_result <- Merge_methy_tcga(dirr)The function ann_merge could merge the copy number variation data downloaded from TCGA using gdc. For example:
metadatafile_name <- "metadata.cart.2018-11-09.json"
jieguo2 <- ann_merge(dirr = system.file(file.path("extdata","cnv"),package="GeoTcgaData"),metadatafile=metadatafile_name)The parameter dirr is a string for the direction of copy number variation data downloaded from TCGA. The parameter metadatafile is the metadata file download from TCGA. The function prepare_chi and differential_cnv could do chi-square test to find copy number variation differential genes. For example:
jieguo3 <- matrix(c(-1.09150,-1.47120,-0.87050,-0.50880,
-0.50880,2.0,2.0,2.0,2.0,2.0,2.601962,2.621332,2.621332,
2.621332,2.621332,2.0,2.0,2.0,2.0,2.0,2.0,2.0,2.0,
2.0,2.0,2.0,2.0,2.0,2.0,2.0),nrow=5)
rownames(jieguo3) <- c("AJAP1", "FHAD1", "CLCNKB", "CROCCP2", "AL137798.3")
colnames(jieguo3) <- c("TCGA-DD-A4NS-10A-01D-A30U-01", "TCGA-ED-A82E-01A-11D-A34Y-01",
"TCGA-WQ-A9G7-01A-11D-A36W-01", "TCGA-DD-AADN-01A-11D-A40Q-01",
"TCGA-ZS-A9CD-10A-01D-A36Z-01", "TCGA-DD-A1EB-11A-11D-A12Y-01")
rt <- prepare_chi(jieguo3)
chiResult <- differential_cnv(rt)The parameter of prepare_chi is the result of function ann_merge and the parameter of function differential_cnv is the result of prepare_chi.
The function gene_ave could average the expression data of different ids for the same gene in the GEO chip data. For example:
aa <- c("MARCH1","MARC1","MARCH1","MARCH1","MARCH1")
bb <- c(2.969058399,4.722410064,8.165514853,8.24243893,8.60815086)
cc <- c(3.969058399,5.722410064,7.165514853,6.24243893,7.60815086)
file_gene_ave <- data.frame(aa=aa,bb=bb,cc=cc)
colnames(file_gene_ave) <- c("Gene", "GSM1629982", "GSM1629983")
result <- gene_ave(file_gene_ave, 1)Multiple genes symbols may correspond to a same chip id. The result of function rep1 is to assign the expression of this id to each gene, and function rep2 deletes the expression. For example:
aa <- c("MARCH1 /// MMA","MARC1","MARCH2 /// MARCH3",
"MARCH3 /// MARCH4","MARCH1")
bb <- c("2.969058399","4.722410064","8.165514853","8.24243893","8.60815086")
cc <- c("3.969058399","5.722410064","7.165514853","6.24243893","7.60815086")
input_file <- data.frame(aa=aa,bb=bb,cc=cc)
rep1_result <- rep1(input_file," /// ")
rep2_result <- rep2(input_file," /// ")id_conversion_vector could convert gene id from one of symbol, RefSeq_ID, Ensembl_ID, NCBI_Gene_ID, UCSC_ID, and UniProt_ID , etc. to another. Use id_ava() to get all the convertible ids. For example:id_conversion_vector("symbol", "ensembl_gene_id", c("A2ML1", "A2ML1-AS1", "A4GALT", "A12M1", "AAAS"))
#> 80% were successfully converted.
#> from to
#> 1 A2ML1 ENSG00000166535
#> 2 A2ML1-AS1 ENSG00000256661
#> 3 A4GALT ENSG00000128274
#> 4 A12M1 <NA>
#> 5 AAAS ENSG00000094914When the user converts the Ensembl ID to other ids, the version number needs to be removed. For example, “ENSG00000186092.4” doesn’t work, you need to change it to “ENSG00000186092”.
Especially, the function id_conversion could convert ENSEMBL gene id to gene Symbol in TCGA. For example:
result <- id_conversion(profile)The parameter profile is a data.frame or matrix of gene expression data in TCGA.
countToFpkm_matrix and countToTpm_matrix could convert count data to FPKM or TPM data.lung_squ_count2 <- matrix(c(1,2,3,4,5,6,7,8,9),ncol=3)
rownames(lung_squ_count2) <- c("DISC1","TCOF1","SPPL3")
colnames(lung_squ_count2) <- c("sample1","sample2","sample3")
jieguo <- countToFpkm_matrix(lung_squ_count2)lung_squ_count2 <- matrix(c(0.11,0.22,0.43,0.14,0.875,0.66,0.77,0.18,0.29),ncol=3)
rownames(lung_squ_count2) <- c("DISC1","TCOF1","SPPL3")
colnames(lung_squ_count2) <- c("sample1","sample2","sample3")
jieguo <- countToTpm_matrix(lung_squ_count2)tcga_cli_deal could combine clinical information obtained from TCGA and extract survival data. For example:tcga_cli <- tcga_cli_deal(system.file(file.path("extdata","tcga_cli"),package="GeoTcgaData"))