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
-
Evaluation of Angelica decursiva reference genes under various stimuli for RT-qPCR data normalization
by: Yuedong He, et al.
Published: (2021-09-01) -
Validation of reference genes for the normalization of the RT-qPCR in peripheral blood mononuclear cells of septic patients
by: Ruoyu Song, et al.
Published: (2023-04-01) -
Screening of reliable reference genes for the normalization of RT-qPCR in chicken gastrointestinal tract
by: Jianfei Chen, et al.
Published: (2023-12-01) -
Validation of Suitable Reference Genes for RT-qPCR Data in Achyranthes bidentata Blume under Different Experimental Conditions
by: Jinting Li, et al.
Published: (2017-05-01) -
Validation of reference genes for the normalization of the RT-qPCR in peripheral blood mononuclear cells of patients with Takayasu arteritis
by: TIAN Yi-xiao, LI Jing
Published: (2021-01-01)