Entering edit mode
4.9 years ago
maria2019
▴
250
I have the 'meth' object for my samples and I wanted to see more PCAs. I realized that PCs from PCASamples are different from what I calculate:
Using PCASamples():
library(methylKit)
meth <-readRDS(file="~/files/meth.rds")
pca <- PCASamples(meth, obj.return=TRUE)
pca$x
PC1 PC2 PC3 PC4 PC5 PC6 sample1 54.7917242 78.835727 -146.389741 -88.0073775 -129.179034 -48.83519 sample2 45.8439749 79.986099 -132.748956 -115.7681777 -182.780012 -18.20983 sample3 -35.5084338 359.737490 -139.675979 340.2946409 178.827413 -49.74668 sample4 -0.8435795 169.940509 -87.345883 84.1664145 56.099736 -58.92960
Using prcomp():
library(methylKit)
meth <-readRDS(file="~/files/meth.rds")
mat=percMethylation(meth)
pca <- prcomp(mat)
pca
PC1 PC2 PC3 PC4 PC5 Sample1 -0.2238237 0.0888081766 -0.27426209 2.240539e-01 -0.128535081 Sample2 -0.2242289 0.0725052576 -0.26868740 2.560139e-01 -0.140892847 Sample3 -0.2227445 -0.0067194119 -0.45275679 -3.366611e-01 0.203404391 Sample4 -0.2230264 0.0068922158 -0.34130776 -2.185143e-01 0.139594741
Hi guys - coming late to this, but does anyone know what variables the PCA is using from the meth object?
If you open the meth object it looks there are 34 columns and it is not your usual column 1 samples name and the other columns are variables,
chr start end strand coverage1 numCs1 numTs1 coverage2 numCs2 numTs2 coverage3 numCs3 numTs3 coverage4 numCs4 numTs4 coverage5 numCs5 numTs5 coverage6 numCs6 numTs6 coverage7 numCs7 numTs7 coverage8 numCs8 numTs8 coverage9 numCs9 numTs9 coverage10 numCs10 numTs10
percMethylation look for this function