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Comparison of digital PCR platforms using the molecular marker

Assays of clinical diagnosis and species identification using molecular markers are performed according to a quantitative method in consideration of sensitivity, cost, speed, convenience, and specificity. However, typical polymerase chain reaction (PCR) assay is difficult to quantify and have variou...

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Autores principales: Lee, Cherl-Joon, Shin, Wonseok, Song, Minsik, Shin, Seung-Shick, Park, Yujun, Srikulnath, Kornsorn, Kim, Dong Hee, Han, Kyudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326530/
https://www.ncbi.nlm.nih.gov/pubmed/37704210
http://dx.doi.org/10.5808/gi.23008
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author Lee, Cherl-Joon
Shin, Wonseok
Song, Minsik
Shin, Seung-Shick
Park, Yujun
Srikulnath, Kornsorn
Kim, Dong Hee
Han, Kyudong
author_facet Lee, Cherl-Joon
Shin, Wonseok
Song, Minsik
Shin, Seung-Shick
Park, Yujun
Srikulnath, Kornsorn
Kim, Dong Hee
Han, Kyudong
author_sort Lee, Cherl-Joon
collection PubMed
description Assays of clinical diagnosis and species identification using molecular markers are performed according to a quantitative method in consideration of sensitivity, cost, speed, convenience, and specificity. However, typical polymerase chain reaction (PCR) assay is difficult to quantify and have various limitations. In addition, to perform quantitative analysis with the quantitative real-time PCR (qRT-PCR) equipment, a standard curve or normalization using reference genes is essential. Within the last a decade, previous studies have reported that the digital PCR (dPCR) assay, a third-generation PCR, can be applied in various fields by overcoming the shortcomings of typical PCR and qRT-PCR assays. We selected Stilla Naica System (Stilla Technologies), Droplet Digital PCR Technology (Bio-Rad), and Lab on an Array Digital Real-Time PCR analyzer system (OPTOLANE) for comparative analysis among the various droplet digital PCR platforms currently in use commercially. Our previous study discovered a molecular marker that can distinguish Hanwoo species (Korean native cattle) using Hanwoo-specific genomic structural variation. Here, we report the pros and cons of the operation of each dPCR platform from various perspectives using this species identification marker. In conclusion, we hope that this study will help researchers to select suitable dPCR platforms according to their purpose and resources.
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spelling pubmed-103265302023-07-08 Comparison of digital PCR platforms using the molecular marker Lee, Cherl-Joon Shin, Wonseok Song, Minsik Shin, Seung-Shick Park, Yujun Srikulnath, Kornsorn Kim, Dong Hee Han, Kyudong Genomics Inform Original Article Assays of clinical diagnosis and species identification using molecular markers are performed according to a quantitative method in consideration of sensitivity, cost, speed, convenience, and specificity. However, typical polymerase chain reaction (PCR) assay is difficult to quantify and have various limitations. In addition, to perform quantitative analysis with the quantitative real-time PCR (qRT-PCR) equipment, a standard curve or normalization using reference genes is essential. Within the last a decade, previous studies have reported that the digital PCR (dPCR) assay, a third-generation PCR, can be applied in various fields by overcoming the shortcomings of typical PCR and qRT-PCR assays. We selected Stilla Naica System (Stilla Technologies), Droplet Digital PCR Technology (Bio-Rad), and Lab on an Array Digital Real-Time PCR analyzer system (OPTOLANE) for comparative analysis among the various droplet digital PCR platforms currently in use commercially. Our previous study discovered a molecular marker that can distinguish Hanwoo species (Korean native cattle) using Hanwoo-specific genomic structural variation. Here, we report the pros and cons of the operation of each dPCR platform from various perspectives using this species identification marker. In conclusion, we hope that this study will help researchers to select suitable dPCR platforms according to their purpose and resources. Korea Genome Organization 2023-06-30 /pmc/articles/PMC10326530/ /pubmed/37704210 http://dx.doi.org/10.5808/gi.23008 Text en (c) 2023, Korea Genome Organization https://creativecommons.org/licenses/by/4.0/(CC) This is an open-access article distributed under the terms of the Creative Commons Attribution license(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Cherl-Joon
Shin, Wonseok
Song, Minsik
Shin, Seung-Shick
Park, Yujun
Srikulnath, Kornsorn
Kim, Dong Hee
Han, Kyudong
Comparison of digital PCR platforms using the molecular marker
title Comparison of digital PCR platforms using the molecular marker
title_full Comparison of digital PCR platforms using the molecular marker
title_fullStr Comparison of digital PCR platforms using the molecular marker
title_full_unstemmed Comparison of digital PCR platforms using the molecular marker
title_short Comparison of digital PCR platforms using the molecular marker
title_sort comparison of digital pcr platforms using the molecular marker
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326530/
https://www.ncbi.nlm.nih.gov/pubmed/37704210
http://dx.doi.org/10.5808/gi.23008
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