Open string instantons and relative stable morphisms

We show how topological open string theory amplitudes can be computed by using relative stable morphisms in the algebraic category. We achieve our goal by explicitly working through an example which has been previously considered by Ooguri and Vafa from the point of view of physics. By using the method of virtual localization, we successfully reproduce their results for multiple covers of a holomorphic disc, whose boundary lies in a Lagrangian submanifold of a Calabi-Yau 3-fold, by Riemann surfaces with arbitrary genera and number of boundary components. In particular we show that in the case we consider there are no open string instantons with more than one boundary component ending on the Lagrangian submanifold.Comment: This is the version published by Geometry & Topology Monographs on 22 April 200

On the Critical Behavior of D1-brane Theories

We study renormalization-group flow patterns in theories arising on D1-branes in various supersymmetry-breaking backgrounds. We argue that the theory of N D1-branes transverse to an orbifold space can be fine-tuned to flow to the corresponding orbifold conformal field theory in the infrared, for particular values of the couplings and theta angles which we determine using the discrete symmetries of the model. By calculating various nonplanar contributions to the scalar potential in the worldvolume theory, we show that fine-tuning is in fact required at finite N, as would be generically expected. We further comment on the presence of singular conformal field theories (such as those whose target space includes a ``throat'' described by an exactly solvable CFT) in the non-supersymmetric context. Throughout the analysis two applications are considered: to gauge theory/gravity duality and to linear sigma model techniques for studying worldsheet string theory.Comment: 23 pages in harvmac big, 8 figure

Non-Gaussianity in Island Cosmology

In this paper we fully calculate the non-Gaussianity of primordial curvature perturbation of island universe by using the second order perturbation equation. We find that for the spectral index $n_s\simeq 0.96$, which is favored by current observations, the non-Gaussianity level $f_{NL}$ seen in island will generally lie between 30 $\sim$ 60, which may be tested by the coming observations. In the landscape, the island universe is one of anthropically acceptable cosmological histories. Thus the results obtained in some sense means the coming observations, especially the measurement of non-Gaussianity, will be significant to make clear how our position in the landscape is populated.Comment: 5 pages, 1 eps figure, some discussions added, published versio

On a Conjecture of Givental

These brief notes record our puzzles and findings surrounding Givental's recent conjecture which expresses higher genus Gromov-Witten invariants in terms of the genus-0 data. We limit our considerations to the case of a projective line, whose Gromov-Witten invariants are well-known and easy to compute. We make some simple checks supporting his conjecture.Comment: 13 pages, no figures; v.2: new title, minor change

An asymptotic sampling formula for the coalescent with Recombination

Ewens sampling formula (ESF) is a one-parameter family of probability distributions with a number of intriguing combinatorial connections. This elegant closed-form formula first arose in biology as the stationary probability distribution of a sample configuration at one locus under the infinite-alleles model of mutation. Since its discovery in the early 1970s, the ESF has been used in various biological applications, and has sparked several interesting mathematical generalizations. In the population genetics community, extending the underlying random-mating model to include recombination has received much attention in the past, but no general closed-form sampling formula is currently known even for the simplest extension, that is, a model with two loci. In this paper, we show that it is possible to obtain useful closed-form results in the case the population-scaled recombination rate $\rho$ is large but not necessarily infinite. Specifically, we consider an asymptotic expansion of the two-locus sampling formula in inverse powers of $\rho$ and obtain closed-form expressions for the first few terms in the expansion. Our asymptotic sampling formula applies to arbitrary sample sizes and configurations.Comment: Published in at http://dx.doi.org/10.1214/09-AAP646 the Annals of Applied Probability (http://www.imstat.org/aap/) by the Institute of Mathematical Statistics (http://www.imstat.org

Multi-locus analysis of genomic time series data from experimental evolution.

Genomic time series data generated by evolve-and-resequence (E&R) experiments offer a powerful window into the mechanisms that drive evolution. However, standard population genetic inference procedures do not account for sampling serially over time, and new methods are needed to make full use of modern experimental evolution data. To address this problem, we develop a Gaussian process approximation to the multi-locus Wright-Fisher process with selection over a time course of tens of generations. The mean and covariance structure of the Gaussian process are obtained by computing the corresponding moments in discrete-time Wright-Fisher models conditioned on the presence of a linked selected site. This enables our method to account for the effects of linkage and selection, both along the genome and across sampled time points, in an approximate but principled manner. We first use simulated data to demonstrate the power of our method to correctly detect, locate and estimate the fitness of a selected allele from among several linked sites. We study how this power changes for different values of selection strength, initial haplotypic diversity, population size, sampling frequency, experimental duration, number of replicates, and sequencing coverage depth. In addition to providing quantitative estimates of selection parameters from experimental evolution data, our model can be used by practitioners to design E&R experiments with requisite power. We also explore how our likelihood-based approach can be used to infer other model parameters, including effective population size and recombination rate. Then, we apply our method to analyze genome-wide data from a real E&R experiment designed to study the adaptation of D. melanogaster to a new laboratory environment with alternating cold and hot temperatures