Results 11 to 20 of about 16,155 (172)
Biologia Plantarum, 2020 Reverse transcription quantitative PCR is a widely used method to detect gene expressions. To obtain accurate expression results, the selection of proper reference genes is important and necessary.
C. ZHANG +6 more
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GenORM: Generalizable One-shot Rope Manipulation with Parameter-Aware Policy
, 2023 Due to the inherent uncertainty in their deformability during motion, previous methods in rope manipulation often require hundreds of real-world demonstrations to train a manipulation policy for each rope, even for simple tasks such as rope goal reaching, which hinder their applications in our ever-changing world.
Kuroki, So +9 more
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Biologia Plantarum, 2020 Real time quantitative PCR (qPCR) is a powerful tool for studying the expression of specific genes. The accuracy and reliability of qPCR analysis data require the selection of reference genes with stable expression.
X. ZUO, F.-Q. WANG, X.-R. LI, M.-M. LI
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LEMming: A Linear Error Model to Normalize Parallel Quantitative Real-Time PCR (qPCR) Data as an Alternative to Reference Gene Based Methods. [PDF]
PLoS ONE, 2015 Gene expression analysis is an essential part of biological and medical investigations. Quantitative real-time PCR (qPCR) is characterized with excellent sensitivity, dynamic range, reproducibility and is still regarded to be the gold standard for ...
Ronny Feuer +6 more
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Selection of Reference Genes for Quantitative Real-time PCR Analysis in Canine Mammary Tumors Using the GeNorm Algorithm [PDF]
Veterinary Pathology, 2006 Eleven reference genes (18s ribosomal ribonucleic acid [RNA], 28s ribosomal RNA, ubiquitin, beta-actin, glycerine aldehyde dehydrogenase, ATP-synthase subunit 5B, hydroxymethylbilane synthase, hypoxanthine-phosphoribosyl transferase, ribosomal protein L32, tryptophan 5monooxygenase activation protein (zeta polypeptide), and TATA-Box binding protein ...
B, Etschmann +4 more
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Selection of reference genes for gene expression studies in Siberian Apricot (Prunus sibirica L.) Germplasm using quantitative real-time PCR. [PDF]
PLoS ONE, 2014 Quantitative real time reverse transcription polymerase chain reaction has been applied in a vast range of studies of gene expression analysis. However, real-time PCR data must be normalized with one or more reference genes.
Jun Niu +11 more
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A simple method to assess group difference in RT-qPCR reference gene selection using GeNorm: The case of the placental sex [PDF]
Placenta, 2017 AbstractNormalization with proper reference genes is a crucial step in obtaining accurate mRNA expression levels in RT-qPCR experiments. GeNorm and NormFinder are two commonly used software packages that help in selecting the best reference genes, based on their expression stability.
Joey St-Pierre +2 more
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Selection of reference genes for transcriptional analysis of edible tubers of potato (Solanum tuberosum L.). [PDF]
PLoS ONE, 2015 Potato (Solanum tuberosum) yield has increased dramatically over the last 50 years and this has been achieved by a combination of improved agronomy and biotechnology efforts.
Roberta Fogliatto Mariot +7 more
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Frontiers in Microbiology, 2021 Alicyclobacillus acidoterrestris is a major concern in fruit juice industry due to its spoilage potential of acidic fruit juice. Quantifying the expression levels of functional genes by real-time quantitative polymerase chain reaction (RT-qPCR) is ...
Ning Zhao +6 more
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Scientific Reports, 2021 Reverse transcription-quantitative PCR (RT-qPCR) is an analytical tool for gene expression quantification. Reference genes are not yet available for gene expression analysis during interactions of Ralstonia solanacearum with ‘Hawaii 7996’ (the most ...
Greecy M. R. Albuquerque +7 more
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