Page 68 - Applied Probability
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3. Newton’s Method and Scoring
                                     TABLE 3.5. Classical and Bayesian Allele Frequency Estimates
                                          Allele
                                                                     .0000
                                                            .0000
                                                                              .0000
                                                    .0054
                                             5
                                                    .0053
                                                                     .0003
                                                                              .0006
                                                            .0003
                                                                              .1039
                                                    .2258
                                             6     White   Black   Chicano    Asian          51
                                                            .1351
                                                                     .2083
                                                    .2227   .1380    .2064    .1147
                                             7      .1586   .3703    .3333    .2597
                                                    .1667   .3645    .3301    .2630
                                             8      .1102   .2108    .0677    .0519
                                                    .1105   .2045    .0707    .0609
                                             9      .1425   .1459    .1432    .4416
                                                    .1465   .1498    .1471    .4073
                                            10      .3522   .1378    .2474    .0909
                                                    .3424   .1421    .2445    .1070
                                            11      .0054   .0000    .0000    .0455
                                                    .0057   .0007    .0007    .0404
                                            12      .0000   .0000    .0000    .0065
                                                    .0002   .0002    .0002    .0061
                                          Sample
                                          Size 2n    372     370      384      154
                              2.97, 5.32, 5.26, .27, and .10. The large differences in the estimated α’s
                              suggest that arbitrarily invoking a reference prior with all α’s equal would
                              be a mistake in this problem.
                                Using the estimated α’s, Table 3.5 compares the maximum likelihood es-
                              timates (first row) and posterior mean estimates (second row) of the allele
                              frequencies within each subpopulation. It is noteworthy that all posterior
                              means are within one standard error of the maximum likelihood estimates.
                              (These standard errors are given in Table 2 of [6].) Nonetheless, the empiri-
                              cal Bayes procedure does tend to moderate the extremes in estimated allele
                              frequencies seen in the different subpopulations. In particular, all posterior
                              means are positive. The maximum likelihood estimates suggest that those
                              alleles failing to appear in a sample are absent in the corresponding sub-
                              population. The empirical Bayes estimates suggest more reasonably that
                              such alleles are simply rare in the subpopulation.



                              3.8 Empirical Bayes Estimation of Haplotype
                                     Frequencies


                              Estimation of haplotype frequencies is even more fraught with uncertainty
                              than estimation of allele frequencies. Many haplotypes are so rare that they
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