C. Foy

发表

The External RNA Controls Consortium: a progress report

Kathleen F. Kerr, U. Scherf, R. Irizarry, 2005, Nature Methods.

The applicability of digital PCR for the assessment of detection limits in GMO analysis

C. Foy, M. Burns, A. Burrell, 2010 .

Application of next generation qPCR and sequencing platforms to mRNA biomarker analysis.

Martin S. Taylor, C. Foy, J. Huggett, 2013, Methods.

The use of digital PCR to improve the application of quantitative molecular diagnostic methods for tuberculosis

Fran Van Heuverswyn, C. Foy, J. Huggett, 2016, BMC Infectious Diseases.

RESEARCH ARTICLE Open Access Evaluation of external RNA controls for

C. Foy, A. Devonshire, R. Elaswarapu, 2022 .

International interlaboratory study comparing single organism 16S rRNA gene sequencing data: Beyond consensus sequence comparisons

Steven P Lund, Justin M Zook, Jim Huggett, 2015, Biomolecular detection and quantification.

Pushing the Envelope with Clinical Use of Digital PCR.

Alison S. Devonshire, C. Foy, J. Huggett, 2021, Clinical chemistry.

The Digital MIQE Guidelines

V. Beneš, J. Vandesompele, J. Hellemans, 2013 .

Guidelines for Minimum Information for Publication of Quantitative Digital PCR Experiments

V. Beneš, J. Vandesompele, J. Hellemans, 2013 .

An International Inter-Laboratory Digital PCR Study Demonstrates High Reproducibility for the Measurement of a Rare Sequence Variant

S. Tzonev, L. Saal, T. Forshew, 2016, bioRxiv.

The dangers of using Cq to quantify nucleic acid in biological samples; a lesson from COVID-19.

J. Vandesompele, H. Zeichhardt, C. Foy, 2021, Clinical chemistry.

Instability of 8E5 calibration standard revealed by digital PCR risks inaccurate quantification of HIV DNA in clinical samples by qPCR

C. Foy, J. Huggett, J. Garson, 2017, Scientific Reports.

Development of a Facile Fluorescent Assay for the Detection of 80 Mutations Within the p53 Gene

D. Hodgson, C. Foy, N. Gibson, 2002, Molecular medicine.

Validation of high-throughput single cell analysis methodology.

C. Foy, M. Baradez, D. Marshall, 2014, Analytical biochemistry.

Standardisation of data from real-time quantitative PCR methods – evaluation of outliers and comparison of calibration curves

Carole A Foy, C. Foy, M. Burns, 2005, BMC biotechnology.

A standardised methodology for the extraction and quantification of cell-free DNA in cerebrospinal fluid and application to evaluation of Alzheimer's disease and brain cancers.

Alison S. Devonshire, R. Perneczky, C. Foy, 2022, New biotechnology.

Standardization of Nucleic Acid Tests for Clinical Measurements of Bacteria and Viruses

H. Zeichhardt, C. Foy, H. Parkes, 2014, Journal of Clinical Microbiology.

Validation of reference gene stability for APAP hepatotoxicity studies in different in vitro systems and identification of novel potential toxicity biomarkers.

Alison S. Devonshire, C. Foy, B. Fox, 2010, Toxicology in vitro : an international journal published in association with BIBRA.

Emerging homogeneous DNA-based technologies in the clinical laboratory.

C. Foy, H. Parkes, 2001, Clinical chemistry.

Considerations for accurate gene expression measurement by reverse transcription quantitative PCR when analysing clinical samples

Carole A. Foy, Jim F. Huggett, Rebecca Sanders, 2014, Analytical and Bioanalytical Chemistry.

The digital MIQE guidelines: Minimum Information for Publication of Quantitative Digital PCR Experiments.

Tania Nolan, Jim F Huggett, Jan Hellemans, 2013, Clinical chemistry.

A comparison of miRNA isolation and RT-qPCR technologies and their effects on quantification accuracy and repeatability.

C. Foy, J. Huggett, T. Wilkes, 2013, BioTechniques.

Towards standardisation of cell-free DNA measurement in plasma: controls for extraction efficiency, fragment size bias and quantification

Alison S. Devonshire, C. Foy, J. Huggett, 2014, Analytical and Bioanalytical Chemistry.

Quantification of epigenetic biomarkers: an evaluation of established and emerging methods for DNA methylation analysis

Martin S. Taylor, Alison S. Devonshire, C. Foy, 2014, BMC Genomics.

Assessment of Digital PCR as a Primary Reference Measurement Procedure to Support Advances in Precision Medicine.

Maria Paola Sassi, Tanja Dreo, Jim F Huggett, 2018, Clinical chemistry.

Applicability of RNA standards for evaluating RT-qPCR assays and platforms

Alison S. Devonshire, C. Foy, A. Devonshire, 2011, BMC Genomics.

Development of a highly sensitive liquid biopsy platform to detect clinically-relevant cancer mutations at low allele fractions in cell-free DNA

N. Rosenfeld, Michelle Pugh, John D. Calaway, 2018, PloS one.

Considerations for digital PCR as an accurate molecular diagnostic tool.

Jim F Huggett, Carole A Foy, Simon Cowen, 2015, Clinical chemistry.

Microarray data quality - review of current developments.

Timothy Wilkes, Holger Laux, Carole A Foy, 2007, Omics : a journal of integrative biology.

Pre-analytical processes in medical diagnostics: New regulatory requirements and standards.

Kurt Zatloukal, Peter Riegman, Stefania Gelmini, 2019, New biotechnology.

International Interlaboratory Digital PCR Study Demonstrating High Reproducibility for the Measurement of a Rare Sequence Variant.

Alison S. Devonshire, S. Tzonev, L. Saal, 2017, Analytical chemistry.

Detection of Rare Drug Resistance Mutations by Digital PCR in a Human Influenza A Virus Model System and Clinical Samples

C. Foy, J. Huggett, J. Garson, 2015, Journal of Clinical Microbiology.

Highly reproducible absolute quantification of Mycobacterium tuberculosis complex by digital PCR.

Jim F Huggett, Alison S. Devonshire, Gavin Nixon, 2015, Analytical chemistry.

Comparison of microfluidic digital PCR and conventional quantitative PCR for measuring copy number variation

Alexandra S. Whale, Stephen Ellison, Carole A. Foy, 2012, Nucleic acids research.

Quality assessment of biobanked nucleic acid extracts for downstream molecular analysis.

C. Foy, J. Huggett, Rebecca Sanders, 2012, Biopreservation and biobanking.

Assessing the Accuracy of Quantitative Molecular Microbial Profiling

David J. Studholme, Denise M. O’Sullivan, Carole A. Foy, 2014, International journal of molecular sciences.

Considerations for the development and application of control materials to improve metagenomic microbial community profiling

David J. Studholme, Jim F. Huggett, Thomas Laver, 2013, Accreditation and Quality Assurance.

Applicability of Control Materials To Support Gene Promoter Characterization and Expression in Engineered Cells Using Digital PCR

C. Foy, J. Huggett, José I. Jiménez, 2022, Analytical chemistry.

An international comparability study on quantification of mRNA gene expression ratios: CCQM-P103.1

Alison S. Devonshire, Steven P. Lund, M. Salit, 2016, Biomolecular detection and quantification.

The performance of human cytomegalovirus digital PCR Reference Measurement Procedure in seven External Quality Assessment schemes over four years.

H. Zeichhardt, Fran Van Heuverswyn, P. Corbisier, 2021, Methods.

Consensus guidelines for the validation of qRT-PCR assays in clinical research by the CardioRNA consortium

A. Scherer, J. Hellemans, Y. Devaux, 2022, Molecular therapy. Methods & clinical development.

The development of microarray standards

Carole A Foy, M. T. Andersen, C. Foy, 2005, Analytical and bioanalytical chemistry.

Inter- and intra-laboratory study to determine the reproducibility of toxicogenomics datasets.

Alison S. Devonshire, Yeyejide A. Adeleye, C. Foy, 2011, Toxicology.

Evaluation of Digital PCR for Absolute RNA Quantification

C. Foy, J. Huggett, Rebecca Sanders, 2013, PloS one.

Methods for Applying Accurate Digital PCR Analysis on Low Copy DNA Samples

Alexandra S. Whale, Carole A. Foy, Simon Cowen, 2013, PloS one.

An international comparability study on quantification of total methyl cytosine content.

C. Foy, S. Fujii, I. Yang, 2009, Analytical biochemistry.

Instability of 8E5 calibration standard revealed by digital PCR risks inaccurate quantification of HIV DNA in clinical samples by qPCR

C. Foy, J. Huggett, J. Garson, 2017, Scientific Reports.

Comparative study of sensitivity, linearity, and resistance to inhibition of digital and nondigital polymerase chain reaction and loop mediated isothermal amplification assays for quantification of human cytomegalovirus.

Jim F Huggett, Eleni Nastouli, Gavin Nixon, 2014, Analytical chemistry.

Evaluation of digital PCR for absolute DNA quantification.

Jim F Huggett, Rebecca Sanders, Carole A Foy, 2011, Analytical chemistry.

Comparison of reverse transcription-quantitative polymerase chain reaction methods and platforms for single cell gene expression analysis.

C. Foy, B. Fox, M. Baradez, 2012, Analytical biochemistry.

A pilot study to evaluate the application of a generic protein standard panel for quality control of biomarker detection technologies

C. Foy, Jesus Minguez, H. Valdivia, 2011, BMC Research Notes.

A comparability study of the emerging protein array platforms with established ELISA procedures.

Carole Foy, C. Foy, D. Onley, 2005, Journal of immunological methods.

Relative quantification of experimental data from antigen particle arrays.

C. Foy, Susan N. J. Pang, Michael Walker, 2005, Clinical chemistry.

ARMS allele-specific amplification-based detection of mutant p53 DNA and mRNA in tumors of the breast.

N. J. Gibson, D. Hodgson, C. Foy, 2001, Clinical chemistry.

Evaluation of a novel approach for the measurement of RNA quality

Stephen L. R. Ellison, Alison S. Devonshire, C. Foy, 2010, BMC Research Notes.

A novel approach for evaluating the performance of real time quantitative loop-mediated isothermal amplification-based methods

C. Foy, C. Carder, J. Stephenson, 2014, Biomolecular detection and quantification.

Improved detection of cell surface proteins using an electrochemiluminescent cell-binding assay.

C. Foy, Susan N. J. Pang, Enamul S Ahsan, 2010, Journal of immunological methods.

Inter-laboratory assessment of different digital PCR platforms for quantification of human cytomegalovirus DNA

Mojca Milavec, Jana Žel, Gerwyn M. Jones, 2017, Analytical and Bioanalytical Chemistry.

Applicability of Three Alternative Instruments for Food Authenticity Analysis: GMO Identification

C. Foy, M. Burns, A. Burrell, 2011, Biotechnology research international.

Application of next generation qPCR and sequencing platforms to mRNA biomarker analysis.

Martin S. Taylor, Alison S. Devonshire, C. Foy, 2013, Methods.

Contributions of the EMERALD project to assessing and improving microarray data quality.

Audrey Kauffmann, Martin Kuiper, James Malone, 2011, BioTechniques.

Survey results on nucleic acid tests of infectious diseases : present status and need for rapid and near-patient diagnostics

Alison S. Devonshire, H. Zeichhardt, C. Foy, 2015 .