As I mentioned when I responded to your previous post a while back, I
also get similar 'blocking' patterns in my values (you can see it in the
intensities, not just the residuals). I contacted Alan Williams at
Affymetrix who was involved with the design of the array; he had a
couple if ideas, but has not tried to determine whether they are truly
the cause:
> First, the probes on are arrays are "edge optimized". This means that
> probes are placed on the array such that differences in synthesis steps
> between adjacent features is minimized. As a result probes with similar
> composition end up near each other.
>
> Another possible cause is that we have a number of control type
> probesets (ie antigenomic background controls) as well as a lot of
> development content (ie yeast probesets), the later not being exposed in
> the library files. The layout of this content could explain the patterns
> as well as some controls are only laid out in certain subgrids.
I have not checked with the control probes to see where they lie and if
this explains it (it's a large swath of the array to explain by controls
and development content, though there are a lot of controls). Basically,
I have also not tried to follow up on this.
I found the following from Affymetrix useful for knowing what is
actually contained in different formats (it's a download, each file in
folder is a file type):
https://www.affymetrix.com/support/file_download.affx?onloadforward=/support/developer/fusion/file_formats.zip
It's best when used while also looking at the file (ASCII version).
Best,
Elizabeth
Frank Ziegner wrote:
> Hi everyone,
>
> does anybody know, where to find detailed information about the
> Affymetrix CDF and CEL file format?
>
> I'm less interested in how the probes for the chip (I work with
> HuEx-1_0-st-v2.) were selected, this is almost completely covered in
> this Technote
> <http://www.affymetrix.com/support/technical/technotes/exon_array_design_technote.pdf>.
> I'm more interested in questions like how the features were distributed
> on the chip or if there are calibration markings on the chip for the
> scanner. Maybe then I could explain some pattern in my spatial plots of
> the raw data or the residuals. Attached is a spatial plot of the
> residuals. As discussed some time ago, this plot is not very meaningful
> since only a fraction of probesets were fitted. But nevertheless it
> shouldn't show this sort of vertical separation. Also I would like to
> know, what the blank spots are for.
>
> Also can anybody recommend some literature which describes CDF or CEL
> files in a more general or introductive way? This would be for an
> introduction of "newbies" to this topic.
>
> Thanks,
> Frank
>
> >
>
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>