A quantitative RT-PCR platform for high-throughput expression profiling of 2500 rice transcription factors
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* Corresponding author: Bernd Mueller-Roeber bmr@uni-potsdam.de
Plant Methods 2007, 3:7 doi:10.1186/1746-4811-3-7
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BioMed Central: 8 citations
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Robert G Rutledge, Don Stewart BMC Molecular Biology 2008, 9:96 (30 October 2008) Measurement of template quantity in real-time qPCR using standard curves is prone to error, and the novel linear regression of efficiency method that calculates the amplification efficiency at the onset of each reaction is more accurate.
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