twoddpcr: an R/Bioconductor package and Shiny app for Droplet Digital PCR analysis

被引:22
作者
Chiu, Anthony [1 ]
Ayub, Mahmood [1 ]
Dive, Caroline [1 ]
Brady, Ged [1 ]
Miller, Crispin J. [2 ]
机构
[1] Univ Manchester, Canc Res UK Manchester Inst, Clin & Expt Pharmacol Grp, Manchester M20 4BX, Lancs, England
[2] Univ Manchester, Canc Res UK Manchester Inst, RNA Biol Grp, Manchester M20 4BX, Lancs, England
关键词
CELL-FREE DNA; MUTATIONS;
D O I
10.1093/bioinformatics/btx308
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A Summary: Droplet Digital PCR (ddPCR) is a sensitive platform used to quantify specific nucleic acid molecules amplified by polymerase chain reactions. Its sensitivity makes it particularly useful for the detection of rare mutant molecules, such as those present in a sample of circulating free tumour DNA obtained from cancer patients. ddPCR works by partitioning a sample into individual droplets for which the majority contain only zero or one target molecule. Each droplet then becomes a reaction chamber for PCR, which through the use of fluorochrome labelled probes allows the target molecules to be detected by measuring the fluorescence intensity of each droplet. The technology supports two channels, allowing, for example, mutant and wild type molecules to be detected simultaneously in the same sample. As yet, no open source software is available for the automatic gating of two channel ddPCR experiments in the case where the droplets can be grouped into four clusters. Here, we present an open source R package 'twoddpcr', which uses Poisson statistics to estimate the number of molecules in such two channel ddPCR data. Using the Shiny framework, an accompanying graphical user interface (GUI) is also included for the package, allowing users to adjust parameters and see the results in real-time.
引用
收藏
页码:2743 / 2745
页数:3
相关论文
共 18 条
[1]  
Attali Dean, 2016, F1000Res, V5, P1411
[2]  
Burdukiewicz M., 2017, DPCR DIGITAL PCR ANA
[3]  
Carr D., 2016, hexbin: Hexagonal Binning Routines, p1.27.2
[4]  
Chang W., 2022, Shiny: Web Application Framework for R
[5]   High-Throughput Droplet Digital PCR System for Absolute Quantitation of DNA Copy Number [J].
Hindson, Benjamin J. ;
Ness, Kevin D. ;
Masquelier, Donald A. ;
Belgrader, Phillip ;
Heredia, Nicholas J. ;
Makarewicz, Anthony J. ;
Bright, Isaac J. ;
Lucero, Michael Y. ;
Hiddessen, Amy L. ;
Legler, Tina C. ;
Kitano, Tyler K. ;
Hodel, Michael R. ;
Petersen, Jonathan F. ;
Wyatt, Paul W. ;
Steenblock, Erin R. ;
Shah, Pallavi H. ;
Bousse, Luc J. ;
Troup, Camille B. ;
Mellen, Jeffrey C. ;
Wittmann, Dean K. ;
Erndt, Nicholas G. ;
Cauley, Thomas H. ;
Koehler, Ryan T. ;
So, Austin P. ;
Dube, Simant ;
Rose, Klint A. ;
Montesclaros, Luz ;
Wang, Shenglong ;
Stumbo, David P. ;
Hodges, Shawn P. ;
Romine, Steven ;
Milanovich, Fred P. ;
White, Helen E. ;
Regan, John F. ;
Karlin-Neumann, George A. ;
Hindson, Christopher M. ;
Saxonov, Serge ;
Colston, Bill W. .
ANALYTICAL CHEMISTRY, 2011, 83 (22) :8604-8610
[6]  
Huber W, 2015, NAT METHODS, V12, P115, DOI [10.1038/nmeth.3252, 10.1038/NMETH.3252]
[7]   Low copy target detection by Droplet Digital PCR through application of a novel open access bioinformatic pipeline, 'definetherain' [J].
Jones, Mathew ;
Williams, James ;
Gaertner, Kathleen ;
Phillips, Rodney ;
Hurst, Jacob ;
Frater, John .
JOURNAL OF VIROLOGICAL METHODS, 2014, 202 :46-53
[8]  
Mahalanobis P. C., 1936, P NATL I SCI INDIA, V2, P8
[9]  
Neuwirth Erich, 2022, CRAN
[10]  
Pages H., 2017, S4VECTORS S4 IMPLEME