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4.5 years ago
rozovski.uri
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0
I have microRNA array data that was generated in a platform that is no longer used. Basically these are unnormalized intensity data. The data is in .txt format (rows: geneID, Colum : conditions). I want to use limma to filter and normalize the data but I do notknow how to import into R this type of data.
Thanks, Uri
Please explain some more about the source of the data. For example: which platform / technology was used?
This is a platform that is no longer exist but it is intensity data . It’s raw data (signal intensity) which I need to filter and normalize
Okay, but which platform?; and from where did you obtain the data? - these are important to know for the purpose of normalisation. Are the control probe intensities still in the data?