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Bootstrap Methods: Recent Advances and New Applications

Bootstrap Methods: Recent Advances and New Applications. 2007 Nonparametrics Conference Michael Chernick United BioSource Corporation October 11, 2007. Bootstrap Topics. Introduction to Bootstrap Wide Variety of Applications Confidence regions and hypothesis tests

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Bootstrap Methods: Recent Advances and New Applications

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  1. Bootstrap Methods: Recent Advances and New Applications 2007 Nonparametrics Conference Michael Chernick United BioSource Corporation October 11, 2007

  2. Bootstrap Topics Introduction to Bootstrap Wide Variety of Applications Confidence regions and hypothesis tests Examples of bootstrap applications: (1) P-value adjustment - consulting example, (2) Bioequivalence - Individual Bioequivalence Examples where bootstrap is not consistent and remedies: (1) infinite variance case for a population mean and (2) extreme values Available Software

  3. Introduction The bootstrap is a general method for doing statistical analysis without making strong parametric assumptions. Efron’s nonparametric bootstrap, resamples the original data. It was originally designed to estimate bias and standard errors for statistical estimates much like the jackknife.

  4. Introduction (continued) The bootstrap is similar to earlier techniques which are also called resampling methods: (1) jackknife, (2) cross-validation, (3) delta method, (4) permutation methods, and (5) subsampling..

  5. Introduction (continued) The technique was extended, modified and refined to handle a wide variety of problems including: (1) confidence intervals and hypothesis tests, (2) linear and nonlinear regression, (3) time series analysis and other problems

  6. Introduction (continued) Definition of Efron’s nonparametric bootstrap. Given a sample of n independent identically distributed (i.i.d.) observations X1, X2, …, Xn from a distribution F and a parameter  of the distribution F with a real valued estimator (X1, X2, …, Xn ), the bootstrap estimates the accuracy of the estimator by replacing F with Fn, the empirical distribution, where Fn places probability mass 1/n at each observation Xi.

  7. Introduction (continued) Let X1*, X2*, …, Xn* be a bootstrap sample, that is a sample of size n taken with replacement from Fn . The bootstrap, estimates the variance of (X1, X2, …, Xn ) by computing or approximating the variance of * = (X1*, X2*, …, Xn* ).

  8. Introduction (continued) Statistical Functionals - A functional is a mapping that takes functions into real numbers. Parameters of a distribution can usually be expressed as functionals of the population distribution. Often the standard estimate of a parameter is the same functional applied to the empirical distribution.

  9. Introduction (continued) Statistical Functionals and the bootstrap. A parameter  is a functional T(F) where T denotes the functional and F is a population distribution. An estimator of  is h = T(Fn) where Fn is the empirical distribution function. Many statistical problems involve properties of the distribution of  - h , its mean (bias of h ), variance, median etc.

  10. Introduction (continued) Bootstrap idea: Cannot determine the distribution of  - h but through the bootstrap we can determine, or approximate through Monte Carlo, the distribution of h - *, where * = T(Fn*) and Fn* is the empirical distribution for a bootstrap sample X1*, X2*,…,Xn* (* is a bootstrap estimate of ). Based on k bootstrap samples the Monte Carlo approximation to the distribution of h - * is used to estimate bias, variance etc. for h . In bootstrapping h substitutes for  and * substitutes for h . Called the bootstrap principle.

  11. Introduction (continued) Basic Theory: Mathematical results show that bootstrap estimates are consistent in particular cases. Basic Idea: Empirical distributions behave in large samples like population distributions. Glivenko-Cantelli Theorem tells us this. The smoothness condition is needed to transfer consistency to functionals of Fn, such as the estimate of the parameter .

  12. Wide Variety of Applications Efron and others recognized that through the power of fast computing the Monte Carlo approximation could be used to extend the bootstrap to many different statistical problems .

  13. Wide Variety of Applications (continued) It can estimate process capability indices for non-Gaussian data. It is used to adjust p-values in a variety of multiple comparison situations. It can be extended to problems involving dependent data including multivariate, spatial and time series data and in sampling from finite populations.

  14. Wide Variety of Applications (continued) It also has been applied to problems involving missing data. In many cases, the theory justifying the use of bootstrap (e.g. consistency theorems) has been extended to these non i.i.d. settings. In other cases, the bootstrap has been modified to “make it work.” The general case of confidence interval estimation is a notable example.

  15. Confidence regions and hypothesis tests The percentile method and other bootstrap variations may require 1000 or more bootstrap replications to be very useful. The percentile method only works under special conditions. Bias correction and other adjustments are sometimes needed to make the bootstrap “accurate” and “correct” when the sample size n is small or moderate.

  16. Confidence regions and hypothesis tests (continued) Confidence intervals are accurate or nearly exact when the stated confidence level for the intervals is approximately the long run probability that the random interval contains the “true” value of the parameter. Accurate confidence intervals are said to be correctif they are approximately the shortest length confidence intervals possible for the given confidence level.

  17. Confidence regions and hypothesis tests (continued) The BCa method, the iterated bootstrap (or double bootstrap) and the bootstrap t method are methods for constructing bootstrap confidence intervals that are closer to being exact (accurate) and correct than the percentile method in many circumstances. See Chernick (2007) pp. 57-65 for details on these methods.

  18. Confidence regions and hypothesis tests (continued) Hall and Martin have shown what the rate is that various bootstrap estimates approach their advertised confidence levels as the size n of the original sample increases. They use Edgeworth and Cornish-Fisher expansions to prove these results. See Hall (1992) Chapter 3 or Chernick (2007) Section 3.1 for more discussion of this. See Ewens and Grant (2001) Chapter 12 for another nice treatment and comparison with permutation tests.

  19. Four Methods for Setting Approximate Confidence Intervals for a Real-Valued Parameter 

  20. Hypothesis tests Since there is a 1-1 correspondence between hypothesis tests and confidence intervals, a hypothesis test about a parameter  can be constructed based on a bootstrap confidence interval for . See Chernick (1999 or 2007) Section 3.2. Examples of hypothesis tests can be found in Section 3.3 of Chernick (1999 or 2007). Advice on which method to use is also given in Carpenter and Bithell (2000).

  21. Examples of bootstrap applications P-value adjustment - a consulting example Many problems in the course of a clinical trial involve multiple comparisons or repeated significance tests for a key endpoint at various follow-up times. In these cases, the individual test p-values are not appropriate and p-value adjustment is appropriate. Conservative estimates based on the Bonferroni inequality are often used but sometimes may be too conservative.

  22. P-value Adjustment Application Westfall and Young (1993) have demonstrated useful bootstrap and permutation approaches which work in a wide variety of multiple testing situations. Their methods are implemented in the SAS software package (Version 6.12 or higher) through a procedure called PROC MULTTEST. Chernick has implemented this approach in a number of clinical trials. As a consultant on a particular clinical trial he employed p-value adjustment to determine if results differed significantly depending on the country where the patient was treated.

  23. P-value Adjustment Application (continued) This example is presented in Section 8.5.3 of Chernick (2007). A company conducted a clinical trial for a medical treatment in one country but due to slow enrollment decided to extend the trial to other countries. The initial country we denote as country E. The other four countries are labeled A, B, C and D.

  24. P-value Adjustment Application (continued) Fisher’s exact test was used to compare failure rates for the treatment with failure rates for the control. The primary statistical analysis of the endpoint. In country E, the result showed that the treatment was superior to the control, but this was not the case in the other countries. The client wanted to show that there were differences among countries which made the poolability of the data questionable.

  25. P-value Adjustment Application (continued) They wanted to claim that only the data in country E was relevant to the submission since they were seeking regulatory approval only in country E. This involved comparing treatment success in each country compared to country E.

  26. P-value Adjustment Application (continued) There are 4 relevant pairwise comparisons of other countries with country E. Consequently, the raw p-values from the individual Fisher tests are not appropriate. The raw p-values were compared with the Bonferroni adjustment and the bootstrap adjustment.

  27. P-value Adjustment Application (continued) TABLE 8.1 from Chernick (2007) page 152 Comparison of Treatment Failure Rates Country failure rate A 40% (18/45) B 41% (58/143) C 29% (20/70) D 29% (51/177) E 22% (26/116) TABLE 8.2 from Chernick (2007) page 153 Comparison of p-value adjustments Countries Raw p Bonf. p Boot. p E vs A 0.0307 0.1229 0.0855 E vs B 0.0021 0.0085 0.0062 E vs C 0.3826 1.0000 0.7654 E vs D 0.2776 1.0000 0.6193

  28. P-value Adjustment Application (continued) The raw p-values indicated that failure rate for E was statistically significantly different (lower) from A and B at the 5% level. But results are misleading since they ignore the multiple testing. The Bonferroni bound shows only E and B to be statistically significantly different at the 10% level.

  29. P-value Adjustment Application (continued) But the Bonferroni bound is known to be excessively conservative in many situations. Bootstrap provides an appropriate answer. For the bootstrap estimate we again find that E and B are clearly different but now we find that the p-value for E and A is below 0.10 and so E is statistically significantly better than A at the 10% level.

  30. Individual Bioequivalence The FDA has a Guidance document on how to conduct bioequivalence (bioavailability) trials. Three types of bioequivalence have been defined (1) average bioequivalence, (2) population bioequivalence and (3) individual bioequivalence. Currently the FDA only requires average bioequivalence be shown (a change over past policy). Bootstrap solutions useful in determining individual bioequivalence and population bioequivalence have been devised and shown to be consistent.

  31. Individual Bioequivalence: Model In the model, we consider crossing over twice with the sequence TRR Meaning new treatment first and then the reference treatment 2 times and RTR, reference first followed by new treatment and then the reference again. Consider the following model for pharmacokinetic response in a 2 treatment crossover design using only sequences RTR and TRR randomized 1:1: Yijkl = μ + Fl +Pj + Qk + Wijk + Sikl + εijkl, where μ is the overall mean, Pj is the fixed effect for the jth period with the constraint ∑ Pj = 0, Qk is the fixed effect for the kth sequence with ∑ Qk= 0, Fl is the fixed effect for the lth drug.

  32. Individual Bioequivalence: Model (continued) For these trials we only have two drugs the new and old Formulations denoted T for the new treatment and R for the reference formulation. We also have the constraint that FT + FR = 0. Now Sikl is a random effect of the ith subject in the kth sequence with the lth treatment, Wijk is the fixed interaction between treatment , sequence and period and εijkl is a random noise (error) component with mean 0 independent and identically distributed and independent of all the fixed and random effects. 32

  33. Individual Bioequivalence: Definition Under the linear model given on the previous slides individual bioequivalence is accepted if after testing H0:ΔPB ≤ Δ versus H1: ΔPB > Δ, where ΔPB = PTR – P RR with PTR = prob(|YT-YR| ≤ r) and P RR = prob(|YT - Y’R| ≤ r) where Δ and r are determined fixed constants and Y’R is the observed response the second time the reference treatment is given.

  34. Bootstrap Results for this Trial See Schall and Luus (1993) for a description of a bootstrap hypothesis test for this problem. Pigeot (2001) in a survey article describes the Schall and Luus method in detail, shows that their method is not consistent and modifies it by constructing a bootstrap percentile method confidence interval to use in the test. In an earlier work Shao, Kübler and Pigeot (2000) prove that the bootstrap method Pigeot describes in Pigeot (2001) is consistent.

  35. Examples where the bootstrap fails Athreya (1987) shows that the bootstrap estimate of the sample mean is inconsistent when the population distribution has an infinite variance. Angus (1993) provides similar inconsistency results for the maximum and minimum of a sequence of independent identically distributed observations.

  36. Examples where the bootstrap fails (continued) We shall describe the inconsistency of the bootstrap in these two cases and then provide remedies sample mean with infinite population variance, and (2) maximum term in an i.i.d sequence of observations

  37. Example where the bootstrap fails - Sample Mean with Infinite Population Variance Singh (1981) and Bickel and Freedman (1981) showed that in the case of estimating the mean from an i.i.d. sample with a finite population variance the bootstrap procedure is consistent. In the case of an infinite variance, the population distribution might have a distribution F(x) satisfying 1-F(x) ~ cx- L(x) where L is a slowly varying function as x , c is a nonnegative constant and 0<2. Under these conditions, the sample mean appropriately normalized, converges to a stable distribution.

  38. Example where the bootstrap fails - Sample Mean with Infinite Population Variance (continued) For =2 the variance of F is finite and the central limit applies. For <2 the population variance is infinite. Theorem 1 of Athreya (1987) proves the inconsistency of the bootstrap for the case where 1<<2. The result tells us that when we appropriately normalize the sample mean and apply the bootstrap substitutions the bootstrap version of the normalized mean converges to a random probability distribution and not to the corresponding fixed stable distribution that the sample mean converges to.

  39. Example where the bootstrap fails -Estimating extreme values For i.i.d. random variables Gnedenko’s theorem usually applies to the maximum or minimum values. Gnedenko’s theorem states that when appropriately normalized the minimum value and the maximum value converge to one of three extreme value distribution families. The appropriate family depends on the tail behavior of the population distribution.

  40. Example where the bootstrap fails -Estimating extreme values (continued) Angus (1993) showed that using the appropriate normalization and the bootstrap substitution, the maximum and minimum converge to a random probability distribution and notthe fixed extreme value distribution from Gnedenko’s theorem that the sample extremes converge to.

  41. Bootstrap Remedies In the past decade many of the problems where the bootstrap is inconsistent remedies have been found by researchers to give good modified bootstrap solutions that are consistent. For both problems describe thus far a simple procedure called the m-out-n bootstrap has been shown to lead to consistent estimates .

  42. The m-out-of-n Bootstrap This idea was proposed by Bickel and Ren (1996) for handling doubly censored data. Instead of sampling n times with replacement from a sample of size n they suggest to do it only m times where m is much less than n. To get the consistency results both m and n need to get large but at different rates. We need m=o(n). That is m/n→0 as m and n both → ∞. This method leads to consistent bootstrap estimates in many cases where the ordinary bootstrap has problems, particularly (1) mean with infinite variance and (2) extreme value distributions.

  43. Available Software Resampling Stats from Resampling Stats Inc. (provides basic bootstrap tools in easy to use software and is good as an elementary teaching tool). SPlus from Insightful Corporation ( good for advanced bootstrap techniques such as BCa, easy to use in new Windows based version). The current module Resample is what I use in my bootstrap class at statistics.com. S functions provided by Tibshirani (see Appendix in Efron and Tibshirani text or visit Rob Tibshirani’s web site http:/www.stat-stanford.edu/~tibs)

  44. Available Software (continued) Stata has a bootstrap algorithm available that some users rave about. Mathworks and other examples (see Susan Holmes web page): http:/www-stat.stanford.edu/~susan) or contact her by email SAS macros are available and Proc MULTTEST does bootstrap sampling.

  45. References on confidence intervals and hypothesis tests (1) Chernick, M.R. (1999). Bootstrap Methods: A Practitioner’s Guide. Wiley, New York. (2) Chernick, M.R. (2007). Bootstrap Methods: A Guide for Practitioners and Researchers, 2nd Edition. Wiley, New York. (3) Hall, P. (1992). The Bootstrap and Edgeworth Expansion. Springer-Verlag, New York. (4) Efron, B. (1982) The Jackknife, the Bootstrap and Other Resampling Plans. Society for Industrial and Applied Mathematics CBMS-NSF Regional Conference Series 38, Philadelphia. 45

  46. References on confidence intervals and hypothesis tests (continued) (5) Carpenter, J. and Bithell, J. (2000). Bootstrap confidence intervals: when, which, what? A practical guide for medical statisticians. Statistics in Medicine 19, 1141-1164. (6) Bahadur, R.R. and Savage, L.J. (1956). The nonexistence of certain statistical procedures in nonparametric problems. Annals of Mathematical Statistics 27, 1115-1122. (7) Ewens, W.J. and Grant, G.R. (2001). Statistical Methods in Bioinformatics An Introduction. 46

  47. References on p-value adjustment (1) Chernick, M.R. (2007). Bootstrap Methods: A Guide for Practitioners and Researchers, 2nd Edition. Wiley, New York. (2) Westfall, P. and Young, S. S. (1993). Resampling-Based Multiple Testing: Examples of p-Value Adjustment. Wiley, New York. 47

  48. References for Individual Bioequivalence (1) Chernick, M. R. (2007). Bootstrap Methods: A Guide for Practitioners and Researchers. Wiley, New York. (2) Pigeot, I. (2001). The jackknife and bootstrap in biomedical research – Common principles and possible pitfalls. Drug Information J. 35, 1431-1443. (3) Schall, R., and Luus, H. G. (1993). On population and individual bioequivalence. Statist. Med. 12, 1109-1124. (4) Shao, J., Kübler, and Pigeot, I. (2000). Consistency of the bootstrap procedure in individual bioequivalence. Biometrika 87, 573-585. 48

  49. References on when bootstrap fails (1) Angus, J. E. (1993). Asymptotic theory for bootstrapping the extremes. Communs. Statist. Theory and Methods 22, 15-30. (2) Athreya, K. B. (1987). Bootstrap estimation of the mean in the infinite variance case. Ann. Statist. 15, 724-731. (3) Bickel, P. J. and Freedman, D. A. (1981). Some asymptotic theory for the bootstrap. Ann. Statist. 9, 1196-1217. 49

  50. References on when bootstrap fails (continued) (4) Chernick, M.R. (1999). Bootstrap Methods: A Practitioner’s Guide. Wiley, New York. (5) Chernick, M.R. (2007). Bootstrap Methods: A Guide for Practitioners and Researchers, 2nd Edition. Wiley, New York. (6) Cochran, W. (1977). Sampling Techniques. 3rd ed., Wiley, New York 50

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