Limma: merging two scans of two-color arrays and spot weights
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Serge Eifes ▴ 90
@serge-eifes-2032
Last seen 10.2 years ago
Dear all, We have performed two-color microarray experiments which were scanned at two different intensities (at low and high intensities). Now we want to merge the resulting files using the mergeScansRG function from the limma library. After the merging the weights component is not defined anymore in the resulting RGList object. As we intend to use spot weights for fitting a linear model what might be a possibility to assess those weights (after merging the two scans) from the initial weights? Many thanks in advance. Best Regards, Serge Serge Eifes Laboratoire de Biologie Moleculaire et Cellulaire du Cancer (LBMCC)
Microarray Cancer Microarray Cancer • 697 views
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