We consider the edge statistics of large dimensional deformed rectangular matrices of the form $Y_t=Y+\sqrt{t}X,$ where $Y$ is a $p \times n$ deterministic signal matrix whose rank is comparable to $n$, $X$ is a $p\times n$ random noise matrix with centered i.i.d. entries with variance $n^{-1}$, and $t>0$ gives the noise level. This model is referred to as the interference-plus-noise matrix in the study of massive multiple-input multiple-output (MIMO) system, which belongs to the category of the so-called signal-plus-noise model. For the case $t=1$, the spectral statistics of this model have been studied to a certain extent in the literature \cite{DOZIER20071099,DOZIER2007678,VLM2012}. In this paper, we study the singular value and singular vector statistics of $Y_t$ around the right-most edge of the singular value spectrum in the harder regime $n^{-2/3}\ll t \ll 1$. This regime is harder than the $t=1$ case, because on one hand, the edge behavior of the empirical spectral distribution (ESD) of $YY^\top$ has a strong effect on the edge statistics of $Y_tY_t^\top$ since $t\ll 1$ is ``small", while on the other hand, the edge statistics of $Y_t$ is also not merely a perturbation of those of $Y$ since $t\gg n^{-2/3}$ is ``large". Under certain regularity assumptions on $Y,$ we prove the edge universality, eigenvalues rigidity and eigenvector delocalization for the matrices $Y_tY_t^\top$ and $Y_t^\top Y_t$. These results can be used to estimate and infer the massive MIMO system. To prove the main results, we analyze the edge behavior of the asymptotic ESD for $Y_tY_t^\top$, and establish some sharp local laws on the resolvent of $Y_tY_t^\top$. These results can be of independent interest, and used as useful inputs for many other problems regarding the spectral statistics of $Y_t$.

We develop a new method for deriving local laws for a large class of random matrices. It is applicable to many matrix models built from sums and products of deterministic or independent random matrices. In particular, it may be used to obtain local laws for matrix ensembles that are \emph{anisotropic} in the sense that their resolvents are well approximated by deterministic matrices that are not multiples of the identity. For definiteness, we present the method for sample covariance matrices of the form Q:=TXX∗T∗, where T is deterministic and X is random with independent entries. We prove that with high probability the resolvent of Q is close to a deterministic matrix, with an optimal error bound and down to optimal spectral scales. As an application, we prove the edge universality of Q by establishing the Tracy-Widom-Airy statistics of the eigenvalues of Q near the soft edges. This result applies in the single-cut and multi-cut cases. Further applications include the distribution of the eigenvectors and an analysis of the outliers and BBP-type phase transitions in finite-rank deformations; they will appear elsewhere. We also apply our method to Wigner matrices whose entries have arbitrary expectation, i.e. we consider W+A where W is a Wigner matrix and a Hermitian deterministic matrix. We prove the anisotropic local law for W+A and use it to establish edge universality.

We derive the alternating arm exponents of the critical Ising model. We obtain six different patterns of alternating boundary arm exponents which correspond to the boundary conditions (⊖⊕), (⊖ free) and (free free), and the alternating interior arm exponents.

The stochasticity of gene expression is manifested in the fluctuations of mRNA and protein copy numbers within a cell lineage over time. While data of this type can be obtained for many generations, most mathematical models are unsuitable to interpret such data since they assume non-growing cells. Here we develop a theoretical approach that quantitatively links the frequency content of lineage data to subcellular dynamics. We elucidate how the position, height, and width of the peaks in the power spectrum provide a distinctive fingerprint that encodes a wealth of information about mechanisms controlling transcription, translation, replication, degradation, bursting, promoter switching, cell cycle duration, cell division, gene dosage compensation, and cell size homeostasis. Predictions are confirmed by analysis of single-cell Escherichia coli data obtained using fluorescence microscopy. Furthermore, by matching the experimental and theoretical power spectra, we infer the temperature-dependent gene expression parameters, without the need of measurements relating fluorescence intensities to molecule numbers.

The goal of this paper is to prove rigorous results for the behavior of genealogies in a one-dimensional long range biased voter model introduced by Hallatschek and Nelson [Theor. Pop. Biol. 73 (2008) 158–170]. The first step, which is easily accomplished using results of Mueller and Tribe [Probab. Theory Related Fields 102 (1995) 519–545], is to show that when space and time are rescaled correctly, our biased voter model converges to a Wright–Fisher SPDE. A simple extension of a result of Durrett and Restrepo [Ann. Appl. Probab. 18 (2008) 334–358] then shows that the dual branching coalescing random walk converges to a branching Brownian motion in which particles coalesce after an exponentially distributed amount of intersection local time. Brunet et al. [Phys. Rev. E (3) 76 (2007) 041104, 20] have conjectured that genealogies in models of this type are described by the Bolthausen–Sznitman coalescent, see [Proc. Natl. Acad. Sci. USA 110 (2013) 437–442]. However, in the model we study there are no simultaneous coalescences. Our third and most significant result concerns “tracer dynamics” in which some of the initial particles in the biased voter model are labeled. We show that the joint distribution of the labeled and unlabeled particles converges to the solution of a system of stochastic partial differential equations. A new duality equation that generalizes the one Shiga [In Stochastic Processes in Physics and Engineering (Bielefeld, 1986) (1988) 345–355 Reidel] developed for the Wright–Fisher SPDE is the key to the proof of that result.