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12. Models of Recombination
                              270
                              Example 12.5.1 Chi-Square Model
                                In the chi-square model [1, 5, 10, 21, 22, 33], a fixed number of points is
                              skipped. If every rth point is a χ point, then s i =1 {i=r} and the equilibrium
                              distribution π is uniform on {0, 1,...,r − 1}. The discrete renewal density
                              u n =1 {n=0 mod r} . The expressions for q 0j (t) and p ij (t) simplify to
                                                          &  −λt
                                                            e           j =0
                                                q 0j (t)  =  (λt) r−j  −λt
                                                             (r−j)!  e  j> 0
                              and
                                                                    ∞
                                                      (λt) i−j  −λt  	  (λt) mr+i−j  −λt
                                       p ij (t)=1 {j≤i}      e   +                 e  .
                                                      (i − j)!         (mr + i − j)!
                                                                   m=1
                              This model tends to fit data well.
                              12.6 Chiasma Interference


                              Chiasma interference can be roughly divided into count interference and
                              position interference. Count interference arises when the total number
                              of chiasmata on a chromosome follows a non-Poisson distribution. Position
                              interference arises when the formation of one chiasma actively discourages
                              the formation of other chiasmata nearby. The count-location model exhibits
                              count interference but not position interference. Stationary renewal mod-
                              els exhibit both types of interference and therefore are somewhat better
                              equipped to capture the subtleties of recombination data.
                                Traditionally, geneticists have measured interference by coincidence co-
                              efficients. The coincidence coefficient C(I 1 ,I 2 ) of two adjacent intervals I 1
                              and I 2 is defined as the ratio of the probability of recombination on both
                              intervals to the product of their individual recombination fractions. Based
                              on equations (12.1) and (12.7), this ratio is
                                             1                                           = 0)]
                                C(I 1 ,I 2 )  =  4  [1 − Pr(N I 1  =0) − Pr(N I 2  = 0)+Pr(N I 1  + N I 2  .
                                                     1               1
                                                                     2
                                                     2  [1 − Pr(N I 1  = 0)] [1 − Pr(N I 2  = 0)]
                              The conditions C(I 1 ,I 2 ) < 1 and C(I 1 ,I 2 ) > 1 are referred to as posi-
                              tive and negative interference, respectively. Positive interference occurs
                              when

                                                                                =0),     (12.15)
                                         Pr(N I 1  + N I 2  =0) < Pr(N I 1  =0) Pr(N I 2
                              and negative interference occurs when the reverse inequality obtains. Hal-
                              dane’s model gives equality and exhibits no interference.
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