... and adding to what has already been said, PCA can be distorted by
non-ellipsoidal distributions or small numbers of unusual values.
Careful (chiefly graphical) examination of results is therefore
essential, and usually fairly easy to do. There are robust/resistant
versions of PCA in R, but they
On Dec 10, 2011 at 5:56pm deb wrote:
> My question is, is there any way I can map the PC1, PC2, PC3 to the
> original conditions,
> so that i can still have a reference to original condition labels after
> PCA?
deb,
To add to what Stephen has said. Best to do read up on principal component
anal
By doing PCA you are trying to find a lower dimensional representation
of the major variation structure in your data. You get PC* to represent
the "new" data. If you want to know what loads on the axes then you
need to look at the loadings. These are the link between the original
data and th
Hi:
I have a large dataset mydata, of 1000 rows and 1000 columns. The rows
have gene names and columns have condition names (cond1, cond2, cond3,
etc).
mydata<- read.table(file="c:/file1.mtx", header=TRUE, sep="")
I applied PCA as follows:
data_after_pca<- prcomp(mydata, retx=TRUE, center=TRUE,
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