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Amplification curve analysis: Data-driven multiplexing using real-time digital PCR
File | Description | Size | Format | |
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ac-2020-02253x.R2_Proof_hi.pdf | Accepted version | 5.78 MB | Adobe PDF | View/Open |
Title: | Amplification curve analysis: Data-driven multiplexing using real-time digital PCR |
Authors: | Moniri, A Miglietta, L Malpartida Cardenas, K Pennisi, I Cacho Soblechero, M Moser, N Holmes, A Georgiou, P Rodriguez Manzano, J |
Item Type: | Journal Article |
Abstract: | Information about the kinetics of PCR reactions are encoded in the amplification curve. However, in digital PCR (dPCR), this information is typically neglected by collapsing each amplification curve into a binary output (positive/negative). Here, we demonstrate that the large volume of raw data obtained from realtime dPCR instruments can be exploited to perform data-driven multiplexing in a single fluorescent channel using machine learning methods, by virtue of the information in the amplification curve. This new approach, referred to as amplification curve analysis (ACA), was shown using an intercalating dye (EvaGreen), reducing the cost and complexity of the assay and enabling the use of melting curve analysis for validation. As a case study, we multiplexed 3 carbapenem-resistant genes to show the impact of this approach on global challenges such as antimicrobial resistance. In the presence of single targets, we report a classification accuracy of 99.1% (N = 16188) which represents a 19.7% increase compared to multiplexing based on the final fluorescent intensity. Considering all combinations of amplification events (including coamplifications), the accuracy was shown to be 92.9% (N = 10383). To support the analysis, we derived a formula to estimate the occurrence of co-amplification in dPCR based on multivariate Poisson statistics, and suggest reducing the digital occupancy in the case of multiple targets in the same digital panel. The ACA approach takes a step towards maximizing the capabilities of existing real-time dPCR instruments and chemistries, by extracting more information from data to enable data-driven multiplexing with high accuracy. Furthermore, we expect that combining this method with existing probe-based assays will increase multiplexing capabilities significantly. We envision that once emerging point-of-care technologies can reliably capture real-time data from isothermal chemistries, the ACA method will facilitate the implementation of dPCR outside of the lab. |
Issue Date: | 18-Sep-2020 |
Date of Acceptance: | 3-Sep-2020 |
URI: | http://hdl.handle.net/10044/1/82118 |
DOI: | 10.1021/acs.analchem.0c02253 |
ISSN: | 0003-2700 |
Publisher: | American Chemical Society |
Start Page: | 13134 |
End Page: | 13143 |
Journal / Book Title: | Analytical Chemistry |
Volume: | 92 |
Issue: | 19 |
Copyright Statement: | © 2020 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Anal. Chem., after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.analchem.0c02253 |
Sponsor/Funder: | Imperial College Healthcare NHS Trust- BRC Funding National Institute for Health Research National Institute for Health Research |
Funder's Grant Number: | RDA02 HPRU-2012-10047 HPRU-2012-10047 |
Keywords: | 0301 Analytical Chemistry 0399 Other Chemical Sciences Analytical Chemistry |
Publication Status: | Published |
Online Publication Date: | 2020-09-18 |
Appears in Collections: | Electrical and Electronic Engineering Department of Infectious Diseases Faculty of Medicine Faculty of Engineering |