A Multivariate Growth Curve Model for Ranking Genes in Replicated Time Course Microarray Data

被引:3
作者
Hamid, Jemila S. [1 ,2 ]
Beyene, Joseph [1 ,2 ]
机构
[1] Hosp Sick Children, Toronto, ON, Canada
[2] Univ Toronto, Toronto, ON M5S 1A1, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
growth curve model; moderation; time course microarray; multivariate; CELL LUNG-CANCER; DIFFERENTIALLY EXPRESSED GENES; THIOREDOXIN; P53; SENSITIVITY; DISCOVERY; SURVIVAL; BCL-2; POWER;
D O I
10.2202/1544-6115.1417
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene ranking problem in time course microarray experiments is challenging since gene expression levels between different time points are correlated. This is because, expression values at successive time points are usually taken from the same organism, tissue or culture. Moreover, time dependency of gene expression values is usually of interest and often is the biological problem that motivates the experiment. We propose a multivariate growth curve model for ranking genes and estimating mean gene expression profiles in replicated time course microarray data. The approach takes the within individual correlation as well as the temporal ordering into consideration. Moreover, time is incorporated as a continuous variable in the model to account for the temporal pattern. Polynomial profiles are assumed to describe the time dependence and a transformation incorporating information across the genes is used. A moderated likelihood ratio test is then applied to the transformed data to get a statistic for ranking genes according to the difference in expression profiles among biological groups. The methodology is presented in a general setup and could be used for one sample as well as more than one sample problem. The estimation is done in a multivariate framework in which information from all the groups involved is used for better inference. Moreover, the within individual correlation as well as information across genes entered in the estimation through a moderated covariance matrix. We assess the performance of our method using simulation studies and illustrate the results with publicly available real time course microarray data.
引用
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页数:28
相关论文
共 48 条
  • [1] Microarray data analysis: from disarray to consolidation and consensus
    Allison, DB
    Cui, XQ
    Page, GP
    Sabripour, M
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (01) : 55 - 65
  • [2] BIRRER MJ, 1989, ANNU REV MED, V40, P305
  • [3] Expression of apoptosis regulatory proteins of the Bcl-2 family and p53 in primary resected non-small cell lung cancer
    Borner, MM
    Brousset, P
    Pfanner-Meyer, B
    Bacchi, M
    Vonlanthen, S
    Hotz, MA
    Altermatt, HJ
    Schlaifer, D
    Reed, JC
    Betticher, DC
    [J]. BRITISH JOURNAL OF CANCER, 1999, 79 (5-6) : 952 - 958
  • [4] Extracellular thioredoxin levels are increased in patients with acute lung injury
    Callister, M. E.
    Burke-Gaffney, A.
    Quinlan, G. J.
    Nicholson, A. G.
    Florio, R.
    Nakamura, H.
    Yodoi, J.
    Evans, T. W.
    [J]. THORAX, 2006, 61 (06) : 521 - 527
  • [5] Craiu RV, 2008, STAT SINICA, V18, P861
  • [6] Does Helicobacter pylori infection play a role in lung cancer?
    Ece, F
    Hatabay, NF
    Erdal, N
    Gedik, C
    Guney, C
    Aksoy, F
    [J]. RESPIRATORY MEDICINE, 2005, 99 (10) : 1258 - 1262
  • [7] The mucin muc4 potentiates neuregulin signaling by increasing the cell-surface populations of ErbB2 and ErbB3
    Funes, Melanie
    Miller, Jamie K.
    Lai, Cary
    Carraway, Kermit L., III
    Sweeney, Colleen
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (28) : 19310 - 19319
  • [8] Residuals in the extended growth curve model
    Hamid, JS
    Von Rosen, D
    [J]. SCANDINAVIAN JOURNAL OF STATISTICS, 2006, 33 (01) : 121 - 138
  • [9] HAMID JS, THESIS ACTA U AGR SU
  • [10] HAMID JS, 2005, BIOSTOCHASTICS