Hi,
Got a quick question. Can the FIRMA code for exon array analysis page
be applied to Gene 1.0 ST arrays?
Thanks!
Yu Chuan
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Hi Elizabeth,
Thanks for your comments. They are very helpful!
Best,
Yu Chuan
On Dec 1, 9:39 am, Elizabeth Purdom wrote:
> > Also, what does it mean if the boxplot for a chip's exon-level NUSE
> > suggests that this chip maybe an outlier (i.e. the median is higher
> > th
0 0
$`20091119_UHR_Exon3`$n
[1] 18705
$`20091119_UHR_Exon3`$conf
[1] 0 0
$`20091119_UHR_Exon3`$out
numeric(0)
attr(,"type")
[1] "NUSE"
On Nov 30, 1:28 am, Mark Robinson wrote:
> Hi Yu Chuan.
>
> I'm still mystified by this. Can you check that the PLM was
> suc
18705
$`20091119_UHR_Exon3`$conf
[1] 0 0
$`20091119_UHR_Exon3`$out
numeric(0)
attr(,"type")
[1] "NUSE"
On Nov 24, 9:32 am, Yu Chuan wrote:
> Hi Mark,
>
> Thanks for your prompt reply. Below is my complete R code together
> with error information. I tried what you s
ity across chips, while gene-level NUSE boxplots don't. And
RLE boxplots don't show much heterogeneity either at the exon-level or
gene-level. Could someone give me an idea about why this is the case,
and whether I should define an outlier based on the gene-level or exon-
level NUSE/RL
Any idea about how to fix this? Thanks!
Yu Chuan
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When reporting problems on aroma.affymetrix, make sure 1) to run the latest
version of the package, 2) to report the output of sessionInfo() and
traceback(), and 3) to post a complete code example.
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Hi folks,
I have a question related to this topic. I want to generate gene-level
expression values using the 3' end probes or 5' end probes only. Looks
like creating a custom CDF file containing only the probes I want is
the only way for that. Is it correct?
Thanks
Hi Mark,
Thanks a lot!! Very useful. I think I know what to do now.
Best,
Yu Chuan
On Nov 6, 4:14 am, Mark Robinson wrote:
> Hi Yu Chuan.
>
> Some comments below.
>
> On 3-Nov-09, at 12:36 PM, Yu Chuan wrote:
>
> > Hi all,
>
> > Follow up the below discussi
proach to get chromosome
locations using what I already have, and wonder if anyone has any
suggestion?
Thanks!
Yu Chuan
Hi Shuying,
So for your main question -- how to get a gene name for a transcript
cluster id -- you will probably need to use the Affymetrix annotation
for this, regardless of
Hi,
I followed your human exon array analysis page, but used gcrma for
background correction.
http://groups.google.com/group/aroma-affymetrix/web/human-exon-array-analysis?hl=en
However, I got errors shown below. Also, can I correct for probe
sequence effect, in addition to GC content?
> bc <-
Hi,
I am going to start to analyze some Affy exon arrays. I just checked
the customized CDF file page and found that the latest ones are
developed in Nov. 2007. Is there any more updated versions since then?
Thanks!
Yu Chuan
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