Limits of Performance of Quantitative Polymerase Chain Reaction Systems

被引:3
|
作者
Vikalo, Haris [1 ]
Hassibi, Babak [2 ]
Hassibi, Arjang [1 ]
机构
[1] Univ Texas Austin, Austin, TX 78712 USA
[2] CALTECH, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
Cramer-Rao lower bound; quantitative polymerase chain reaction; BRANCHING-PROCESS; PCR; AMPLIFICATION; REPLICATION; EFFICIENCY; ALGORITHM;
D O I
10.1109/TIT.2009.2037088
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Estimation of the DNA copy number in a given biological sample is an important problem in genomics. Quantitative polymerase chain reaction (qPCR) systems detect the target DNA molecules by amplifying their number through a series of thermal cycles and measuring the amount of created amplicons in each cycle. Ideally, the number of target molecules doubles at the end of each cycle. However, in practice, due to biochemical noise the efficiency of the qPCR reaction-defined as the fraction of the target molecules which are successfully copied during a cycle-is always less than. In this paper, we formulate the problem of the joint maximum-likelihood estimation of the qPCR efficiency and the initial DNA copy number. Then, we analytically determine the limits of performance of qPCR by deriving the Cramer-Rao lower bound on the mean-square estimation error. As indicated by simulation studies, the performance of the proposed estimator is superior compared to competing statistical approaches. The proposed approach is validated using experimental data.
引用
收藏
页码:688 / 695
页数:8
相关论文
共 50 条
  • [1] Quantitative polymerase chain reaction
    Miller, James R. C.
    Andre, Ralph
    BRITISH JOURNAL OF HOSPITAL MEDICINE, 2014, 75 : 13 - 17
  • [2] Plasma Levels of Bacterial DNA in HIV Infection: The Limits of Quantitative Polymerase Chain Reaction
    Ferri, Emanuele
    Novati, Stefano
    Casiraghi, Maurizio
    Sambri, Vittorio
    Genco, Francesca
    Gulminetti, Roberto
    Bandi, Claudio
    JOURNAL OF INFECTIOUS DISEASES, 2010, 202 (01): : 176 - 177
  • [3] Plasma Levels of Bacterial DNA in HIV Infection: The Limits of Quantitative Polymerase Chain Reaction Reply
    Lederman, Michael M.
    Jiang, Wei
    Douek, Danny
    Brenchley, Jason
    JOURNAL OF INFECTIOUS DISEASES, 2010, 202 (01): : 178 - 178
  • [4] An alternative quantitative polymerase chain reaction method
    Nicoletti, A
    SassyPrigent, C
    ANALYTICAL BIOCHEMISTRY, 1996, 236 (02) : 229 - 241
  • [5] A quantitative description of the competitive polymerase chain reaction
    Schnell, S
    Mendoza, C
    SIMULATION MODELLING IN BIOENGINEERING, 1996, : 13 - 22
  • [6] Basics of quantitative polymerase chain reaction: 2. Electrophoresis and quantitation of polymerase chain reaction products
    Sundfors, C.
    Collan, Y.
    Electrophoresis, 17 (01):
  • [7] Basics of quantitative polymerase chain reaction .2. Electrophoresis and quantitation of polymerase chain reaction products
    Sundfors, C
    Collan, Y
    ELECTROPHORESIS, 1996, 17 (01) : 44 - 48
  • [8] Performance of the Nanostring nCounter Compared to a Quantitative Reverse Transcriptase Polymerase Chain Reaction Assay
    Liew, M.
    Seipp, M.
    Voelkerding, K.
    Witwer, C.
    Bernard, P.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2009, 11 (06): : 668 - 668
  • [9] POLYMERASE CHAIN-REACTION IN VIRUS DIAGNOSIS - USES AND LIMITS
    HAAS, L
    TIERAERZTLICHE UMSCHAU, 1992, 47 (04) : 223 - 227
  • [10] A QUANTITATIVE POLYMERASE CHAIN REACTION ANALYSIS SOLUTION IN R
    Ahmed, Adam E.
    Reiss, Allison B.
    Kasselman, Lora J.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2019, 67 (04) : 796 - 796