Robust RT-qPCR data normalization: validation and selection of internal reference genes during post-experimental data analysis.
Reverse transcription and real-time PCR (RT-qPCR) has been widely used for rapid quantification of relative gene expression. To offset technical confounding variations, stably-expressed internal reference genes are measured simultaneously along with target genes for data normalization. Statistic met...
Main Authors: | Daijun Ling, Paul M Salvaterra |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3058000?pdf=render |
Similar Items
-
SASqPCR: robust and rapid analysis of RT-qPCR data in SAS.
by: Daijun Ling
Published: (2012-01-01) -
Identification of Reference Genes for RT-qPCR Data Normalization in Cannabis sativa Stem Tissues
by: Lauralie Mangeot-Peter, et al.
Published: (2016-09-01) -
Identification and Validation of Reference Genes for RT-qPCR Normalization in Mythimna separata (Lepidoptera: Noctuidae)
by: Ke Li, et al.
Published: (2018-01-01) -
RefGenes: identification of reliable and condition specific reference genes for RT-qPCR data normalization
by: Bleuler Stefan, et al.
Published: (2011-03-01) -
Evaluation of Angelica decursiva reference genes under various stimuli for RT-qPCR data normalization
by: Yuedong He, et al.
Published: (2021-09-01)