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  1. Article: Microfluidic droplet-based PCR instrumentation for high-throughput gene expression profiling and biomarker discovery.

    Hayes, Christopher J / Dalton, Tara M

    Biomolecular detection and quantification

    2015  Volume 4, Page(s) 22–32

    Abstract: PCR is a common and often indispensable technique used in medical and biological research labs for a variety of applications. Real-time quantitative PCR (RT-qPCR) has become a definitive technique for quantitating differences in gene expression levels ... ...

    Abstract PCR is a common and often indispensable technique used in medical and biological research labs for a variety of applications. Real-time quantitative PCR (RT-qPCR) has become a definitive technique for quantitating differences in gene expression levels between samples. Yet, in spite of this importance, reliable methods to quantitate nucleic acid amounts in a higher throughput remain elusive. In the following paper, a unique design to quantify gene expression levels at the nanoscale in a continuous flow system is presented. Fully automated, high-throughput, low volume amplification of deoxynucleotides (DNA) in a droplet based microfluidic system is described. Unlike some conventional qPCR instrumentation that use integrated fluidic circuits or plate arrays, the instrument performs qPCR in a continuous, micro-droplet flowing process with droplet generation, distinctive reagent mixing, thermal cycling and optical detection platforms all combined on one complete instrument. Detailed experimental profiling of reactions of less than 300 nl total volume is achieved using the platform demonstrating the dynamic range to be 4 order logs and consistent instrument sensitivity. Furthermore, reduced pipetting steps by as much as 90% and a unique degree of hands-free automation makes the analytical possibilities for this instrumentation far reaching. In conclusion, a discussion of the first demonstrations of this approach to perform novel, continuous high-throughput biological screens is presented. The results generated from the instrument, when compared with commercial instrumentation, demonstrate the instrument reliability and robustness to carry out further studies of clinical significance with added throughput and economic benefits.
    Language English
    Publishing date 2015-06-06
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2821770-6
    ISSN 2214-7535
    ISSN 2214-7535
    DOI 10.1016/j.bdq.2015.04.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effect of substrate thermal resistance on space-domain microchannel fluorescent melting curve analysis.

    Kinahan, David J / Dalton, Tara M / Davies, Mark R D

    Biomedical microdevices

    2009  Volume 11, Issue 4, Page(s) 747–754

    Abstract: In recent years, Fluorescent Melting Curve Analysis (FMCA) has become an almost ubiquitous feature of commercial quantitative PCR (qPCR) thermal cyclers. Here a micro-fluidic device is presented capable of performing FMCA within a microchannel. The ... ...

    Abstract In recent years, Fluorescent Melting Curve Analysis (FMCA) has become an almost ubiquitous feature of commercial quantitative PCR (qPCR) thermal cyclers. Here a micro-fluidic device is presented capable of performing FMCA within a microchannel. The device consists of modular thermally conductive blocks which can sandwich a microfluidic substrate. Opposing ends of the blocks are held at differing temperatures and a linear thermal gradient is generated along the microfluidic channel. Fluorescent measurements taken from a sample as it passes along the micro-fluidic channel permits fluorescent melting curves to be generated. In this study we measure DNA melting temperature from two plasmid fragments. The effects of flow velocity and ramp-rate are investigated, and measured melting curves are compared to those acquired from a commercially available PCR thermocycler.
    MeSH term(s) Fluorescence ; Hot Temperature ; Microfluidic Analytical Techniques/instrumentation ; Microfluidic Analytical Techniques/methods ; Plasmids/chemistry ; Polymerase Chain Reaction/instrumentation ; Polymerase Chain Reaction/methods ; Sequence Analysis, DNA/instrumentation ; Sequence Analysis, DNA/methods
    Language English
    Publishing date 2009-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2004019-2
    ISSN 1572-8781 ; 1387-2176
    ISSN (online) 1572-8781
    ISSN 1387-2176
    DOI 10.1007/s10544-009-9288-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Extracellular matrix gene expression profiling using microfluidics for colorectal carcinoma stratification.

    Hayes, Christopher J / Dowling, Catriona M / Dwane, Susan / McCumiskey, Mary E / Tormey, Shona M / Anne Merrigan, B / Coffey, John C / Kiely, Patrick A / Dalton, Tara M

    Biomicrofluidics

    2016  Volume 10, Issue 5, Page(s) 54124

    Abstract: In cancer, biomarkers have many potential applications including generation of a differential diagnosis, prediction of response to treatment, and monitoring disease progression. Many molecular biomarkers have been put forward for different diseases but ... ...

    Abstract In cancer, biomarkers have many potential applications including generation of a differential diagnosis, prediction of response to treatment, and monitoring disease progression. Many molecular biomarkers have been put forward for different diseases but most of them do not possess the required specificity and sensitivity. A biomarker with a high sensitivity has a low specificity and vice versa. The inaccuracy of the biomarkers currently in use has led to a compelling need to identify more accurate markers with diagnostic and prognostic significance. The aim of the present study was to use a novel, droplet-based, microfluidic platform to evaluate the prognostic value of a panel of thirty-four genes that regulate the composition of extracellular matrices in colorectal carcinoma. Our method is a novel approach as it uses using continuous-flowing Polymerase Chain Reaction for the sensitive detection and accurate quantitation of gene expression. We identified a panel of relevant extracellular matrix genes whose expression levels were measured by real-time quantitative polymerase chain reaction using Taqman
    Language English
    Publishing date 2016-10-31
    Publishing country United States
    Document type Journal Article
    ISSN 1932-1058
    ISSN 1932-1058
    DOI 10.1063/1.4966245
    Database MEDical Literature Analysis and Retrieval System OnLINE

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