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Bayesian dynamic modeling of latent trait distributions

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Bayesian dynamic modeling of latent trait distributions Paper by David B. Dunson, Biostatistics, 2006 Duke University Machine Learning Group Presented by Kai Ni – PowerPoint PPT presentation

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Title: Bayesian dynamic modeling of latent trait distributions


1
Bayesian dynamic modeling of latent trait
distributions
Paper by David B. Dunson, Biostatistics, 2006
Duke University Machine Learning Group Presented
by Kai Ni Jan. 25, 2007
2
Outline
  • Introduction
  • Measurement model
  • Dynamic mixture of Dirichlet processes
  • Inference
  • Results Conclusion

3
Motivation
  • The general problem
  • The primary response variable of interest cannot
    be measured directly and one must rely on
    multiple surrogates.
  • The different measured outcomes are assumed to e
    manifestations of a latent variable, which may
    depend on covaraites.
  • Example Cannot measure the frequency of DNA
    strand break but can use gel electrophoresis to
    get surrogates. The distribution of DNA damage
    across cells may have different shapes depending
    on the level of oxidative stress.

4
Motivation (2)
  • The paper focus on developing an approach for
    assessing dynamic changes in the latent response
    distribution across levels of a predictor.
  • Dynamic mixture of Dirichlet processes (DMDP)
    The latent response distribution in group h is
    represented as a mixture of the distribution in
    group h-1 and an unknown innovation distribution,
    which is assigned a DP prior.

5
Measurement Model
  • Let yhi (yhi1,,yhip) denote a p x 1 vector of
    surrogate measurements for the latent response of
    the ith (i 1,,nh) subject in group h (h
    1,,d).
  • For example, in the DNA damage study, yhi denotes
    surrogates of DNA damage for the ith cell in dose
    group h.
  • The yhi has both continuous and categorical
    elements. Use some mapping function to get an
    underlying continuous variables yhi.

6
Measurement Model (2)
  • Relate the underlying continuous variables to the
    latent response through a measurement model
  • Latent variable
  • Intercept parameters
  • Factor loadings
  • Measurement errors
  • A scale mixture of normal distribution is
    assumed for the residual distribution.
  • The primary goal is to assess how the latent
    response distribution changes between groups.

7
Dynamic mixture of Dirichlet process
  • First the latent response distribution for group
    1 is assumed to be drawn from a DP
  • and the predictive density of latent response
    for group 1 is
  • Assume the distribution G2 for group 2 shares
    features with G1 but that innovation may have
    occurred. So G2
  • G2 is randomly modified from G1 by (1) reducing
    the probabilities allocated to the atoms in G1 by
    a factor (1- ) and (2) incorporating new atoms
    drawn from the base

8
DMDP
  • The difference between G1 and G2 has mean and
    variance
  • The hyperparameters control
    the magnitude of the expected changed from G1 to
    G2.

9
DMDP
10
Correlation
  • For the special case in which
    for all l, so that the same base distribution is
    chosen for each component in the mixture. The
    correlation between consecutive Gs is
  • The prior probability of clustering together two
    subjects h, i and h, i in the same or different
    groups is
  • For the hyperparameters, beta distribution is
    chosen for and gamma distribution is chosen
    for

11
Sampling in the latent response model
12
Sampling in the measurement model
13
Inference on the latent response distribution
  • Collecting draws from the conditional predictive
    distribution for a future subject in dose groups
  • After convergence, the samples of nh,nh1
    represent draws from the predictive density of
    the latent response in group h, and inferences
    can be based on comparing these densities between
    groups.

14
DNA damage study
  • The study assessed the effect of oxidative stress
    on the frequency of DNA strand breaks using
    single-cell gel electrophoresis.
  • 500 human lymphoblastoid cells drawn from an
    immortalized cell line were randomized to one of
    the the five dose groups (0, 5, 20, 50, or 100
    micromoles H2O2).
  • There are p5 surrogate measures of DNA damage,
    including (1) tail DNA, (2) tail extent divided
    by head extent, (3) extent tail moment, (4) Olive
    tail moment, and (5) tail extent.

15
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16
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17
Conclusion
  • The author proposed a Bayesian semiparametric
    latent response model in which the latent
    variable density can shift dynamically across
    groups.
  • Use linear regression model to infer the latent
    variables may fail in many applications while the
    measurement model proposed by the author is quite
    flexible.
  • The DMDP should prove useful when interest
    focuses on clustering of observations within and
    across groups.
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