The goal of cancer genome sequencing projects is to determine the genetic
alterations that cause common cancers. Many malignancies arise during the
clonal expansion of a benign tumor which motivates the study of recurrent
selective sweeps in an exponentially growing population. To better understand
this process, Beerenwinkel et al. [PLoS Comput. Biol. 3 (2007) 2239--2246]
consider a Wright--Fisher model in which cells from an exponentially growing
population accumulate advantageous mutations. Simulations show a traveling wave
in which the time of the first k-fold mutant, Tk, is approximately linear
in k and heuristics are used to obtain formulas for ETk. Here, we consider
the analogous problem for the Moran model and prove that as the mutation rate
μ→0, Tk∼cklog(1/μ), where the ck can be computed
explicitly. In addition, we derive a limiting result on a log scale for the
size of Xk(t)=the number of cells with k mutations at time t.Comment: Published in at http://dx.doi.org/10.1214/10-AAP721 the Annals of
Applied Probability (http://www.imstat.org/aap/) by the Institute of
Mathematical Statistics (http://www.imstat.org