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Selection of DDX5 as a novel internal control for Q-RT-PCR from microarray data using a block bootstrap re-sampling scheme

BACKGROUND: The development of microarrays permits us to monitor transcriptomes on a genome-wide scale. To validate microarray measurements, quantitative-real time-reverse transcription PCR (Q-RT-PCR) is one of the most robust and commonly used approaches. The new challenge in gene quantification an...

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Detalles Bibliográficos
Autores principales:	Su, Li-Jen, Chang, Ching-Wei, Wu, Yu-Chung, Chen, Kuang-Chi, Lin, Chien-Ju, Liang, Shu-Ching, Lin, Chi-Hung, Whang-Peng, Jacqueline, Hsu, Shih-Lan, Chen, Chen-Hsin, Huang, Chi-Ying F
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2007
Materias:	Methodology Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894975/ https://www.ncbi.nlm.nih.gov/pubmed/17540040 http://dx.doi.org/10.1186/1471-2164-8-140

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