Hi I need help since I have never worked on RT PCR data before . I have 8 data files each corresponding to a single pcr run. Each file also represent 10 samples(5 cancer and 5 healthy) belonging to a unique gene. I have 7 unique genes and 1 reference (total 8 files). Can any body help me with preproceesing and normalization? -- View this message in context: http://www.nabble.com/Real-Time-PCR-data-analysis-help-tp24577344p24577344.html Sent from the R help mailing list archive at Nabble.com.
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