Quality Images Website moved
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Ben Bolstad ★ 1.2k
@ben-bolstad-1494
Last seen 6.7 years ago
The gallery of quality images from fitPLM has moved to http://plmimagegallery.bmbolstad.com/ As always, contributions are welcome.
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David Ruau ▴ 110
@david-ruau-1473
Last seen 9.7 years ago
Dear Dr. Bolstad, Thanks for those really interesting gallery, it make you feel less alone when you have a look at your own chips after. I would like to know if a tool exist to remove the badly hybridized zone of the chip from the analysis? I mean just keeping the good zone of the chip or do not include the bad zone into the rest of the analysis. I motivated by this problem because my boss always gnash one's teeth when I say that this chip is bad and we should not use it. David On Nov 10, 2005, at 1:03, Ben Bolstad wrote: > The gallery of quality images from fitPLM has moved to > > http://plmimagegallery.bmbolstad.com/ > > As always, contributions are welcome. > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor >
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Hi David, To actually decide whether or not to remove a chip from a dataset the recommended method is to use either or both of the RLE and NUSE boxplots and look for arrays with boxes that are centered higher or more spread than the others. The chip pseudo-images give you the ability to potentially diagnose the cause of the lesser quality data. Generally speaking, smaller artifacts are not problematic (and probably aren't even reflected in the NUSE or RLE) although they can sometimes be interesting as can be seen by some of the images in the gallery. This is because on most modern chips the probes making up each probeset are distributed all across the array, which means that there is typically only one probe in any probeset affected. Thus provided you are using a robust expression measure eg RMA or the expression values from fitPLM itself you won't have any problem. Larger artifacts are more problematic (and usually you'll find correspond with NUSE and RLE) because it typically means there are some probesets with a large number of probes being affected. If it is really bad you probably don't have much choice but to remove the whole chip from subsequent analysis. If you feel you are somewhere in between then your best option is probably to do some down-weighting of lesser quality data. I believe if you do your analysis using limma and supply the PLMset from fitPLM it will do something like this, though you might have other ideas about how to do the weighting. I think this would be a better approach then just completely masking the area. Thanks, Ben On Thu, 2005-11-17 at 10:32 +0100, David Ruau wrote: > Dear Dr. Bolstad, > > Thanks for those really interesting gallery, it make you feel less > alone when you have a look at your own chips after. > I would like to know if a tool exist to remove the badly hybridized > zone of the chip from the analysis? > I mean just keeping the good zone of the chip or do not include the bad > zone into the rest of the analysis. > > I motivated by this problem because my boss always gnash one's teeth > when I say that this chip is bad and we should not use it. > > David > > On Nov 10, 2005, at 1:03, Ben Bolstad wrote: > > > The gallery of quality images from fitPLM has moved to > > > > http://plmimagegallery.bmbolstad.com/ > > > > As always, contributions are welcome. > > > > _______________________________________________ > > Bioconductor mailing list > > Bioconductor at stat.math.ethz.ch > > https://stat.ethz.ch/mailman/listinfo/bioconductor > > > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor
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Thanks for your answer! Another question more the community in general: Do you think we can ask Affymetrix to send us another chip when we do have a considerable artifact which is only visible with the help of the false color image? Here we already did that when the chip was having a visible scratch on the scan picture (= the regular one in B&W). David On Nov 17, 2005, at 17:46, Ben Bolstad wrote: > Hi David, > > To actually decide whether or not to remove a chip from a dataset the > recommended method is to use either or both of the RLE and NUSE > boxplots > and look for arrays with boxes that are centered higher or more spread > than the others. > > The chip pseudo-images give you the ability to potentially diagnose the > cause of the lesser quality data. Generally speaking, smaller artifacts > are not problematic (and probably aren't even reflected in the NUSE or > RLE) although they can sometimes be interesting as can be seen by some > of the images in the gallery. This is because on most modern chips the > probes making up each probeset are distributed all across the array, > which means that there is typically only one probe in any probeset > affected. Thus provided you are using a robust expression measure eg > RMA > or the expression values from fitPLM itself you won't have any problem. > > Larger artifacts are more problematic (and usually you'll find > correspond with NUSE and RLE) because it typically means there are some > probesets with a large number of probes being affected. If it is really > bad you probably don't have much choice but to remove the whole chip > from subsequent analysis. > > If you feel you are somewhere in between then your best option is > probably to do some down-weighting of lesser quality data. I believe if > you do your analysis using limma and supply the PLMset from fitPLM it > will do something like this, though you might have other ideas about > how > to do the weighting. I think this would be a better approach then just > completely masking the area. > > > Thanks, > > Ben > > > On Thu, 2005-11-17 at 10:32 +0100, David Ruau wrote: >> Dear Dr. Bolstad, >> >> Thanks for those really interesting gallery, it make you feel less >> alone when you have a look at your own chips after. >> I would like to know if a tool exist to remove the badly hybridized >> zone of the chip from the analysis? >> I mean just keeping the good zone of the chip or do not include the >> bad >> zone into the rest of the analysis. >> >> I motivated by this problem because my boss always gnash one's teeth >> when I say that this chip is bad and we should not use it. >> >> David >> >> On Nov 10, 2005, at 1:03, Ben Bolstad wrote: >> >>> The gallery of quality images from fitPLM has moved to >>> >>> http://plmimagegallery.bmbolstad.com/ >>> >>> As always, contributions are welcome. >>> >>> _______________________________________________ >>> Bioconductor mailing list >>> Bioconductor at stat.math.ethz.ch >>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>> >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at stat.math.ethz.ch >> https://stat.ethz.ch/mailman/listinfo/bioconductor > >
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