2022
DOI: 10.3390/life12030386
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Obtaining Reliable RT-qPCR Results in Molecular Diagnostics—MIQE Goals and Pitfalls for Transcriptional Biomarker Discovery

Abstract: In this review, we discuss the development pipeline for transcriptional biomarkers in molecular diagnostics and stress the importance of a reliable gene transcript quantification strategy. Hence, a further focus is put on the MIQE guidelines and how to adapt them for biomarker discovery, from signature validation up to routine diagnostic applications. First, the advantages and pitfalls of the holistic RNA sequencing for biomarker development will be described to establish a candidate biomarker signature. Seque… Show more

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Cited by 16 publications
(9 citation statements)
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“…Influenza is highly contagious worldwide and prevalent among high-risk groups, necessitating timely and accurate diagnosis [1,21]. Currently, the RT-qPCR test is considered the gold standard for its accuracy [22]. However, it is not suitable for field inspection due to the significant time, cost and specialized equipment required [23].…”
Section: Discussionmentioning
confidence: 99%
“…Influenza is highly contagious worldwide and prevalent among high-risk groups, necessitating timely and accurate diagnosis [1,21]. Currently, the RT-qPCR test is considered the gold standard for its accuracy [22]. However, it is not suitable for field inspection due to the significant time, cost and specialized equipment required [23].…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, considering gene expression as the upstream molecule of the signaling regulatory pathway proves to be a more stable and suitable biomarker for disease diagnosis and prognosis. Moreover, qRT-PCR demonstrates its value as a tool in establishing disease-specific biomarkers in clinical settings due to its accuracy, speed, and relatively straightforward process, taking about 6 h from sample preparation to obtaining results [44].…”
Section: Discussionmentioning
confidence: 99%
“…Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats INTRODUCTION R eal-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) measurement of transcript abundance has become the method of choice for highthroughput and accurate expression monitoring of chosen genes due to its high sensitivity, specificity, and broad quantification range [1][2][3] . This approach is most often employed for molecular diagnostics, verifying microarray data of a narrower collection of genes and is especially beneficial when just a limited number of cells or tissue samples are available [2,4] . The expression of the gene of interest (GOI) is compared to that of an internal control gene known as a housekeeping gene (HKG) to obtain quantification.…”
Section: •Basic Research•mentioning
confidence: 99%