[BioC] (no subject)
Rafael A. Irizarry
ririzarr at jhsph.edu
Tue Jun 3 00:46:18 MEST 2003
On Mon, 2 Jun 2003 alea at interfree.it wrote:
>
> Laurent Gautier <laurent at cbs.dtu.dk> wrote:
>
> > One should keep in mind the assumption behind many of the normalization
> > techniques: "most of the genes are not differentially expressed across
> > the
> > experiments". Filtering before normalization/scaling should be done with
> > that in mind.
>
> Hi all.
> I'm a novice,... may be this is he reason why I'm loosing myself..
> What is a "low espressed spot"?
> It seems a problem of logic.
a better way to say it is "low intensity spot". low intesities are usually
due to low expression of the gene or probe represented by the spot.
>
> It seems to me that on one side we say that it not an expressed gene (=
we can not consider as an expressed gene), it's more likely dued to noise
(background,...).
>
but where (and how) do you draw the line?
> On the other side we say that, however, it's actually an expression and
good for normalizing.
> Of course a non expressed gene is also not differentially expressed...
what if its non-expressed on one array and expressed on another? i would
call this differentially expressed.
>
> Are good enougth for normalization and not enougth for other analysis?
> Is it another cut-off problem??
>
> Absent -
> So and so (for normalizing yes, other analysis no) -
> Present -
>
normalization techiniques that use all genes or probes appear to work
succesfully in practice. papers by dudoit, bolstad, aastrad, li and wong,
huber, and various others demonstrate this.
> AleA
>
>
>
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>
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