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Paula Tataru

Publications and source records attributed to Paula Tataru.

4 recordsLinked to original sources

Inference of distribution of fitness effects and proportion of adaptive substitutions from polymorphism data

The distribution of fitness effects (DFE) encompasses deleterious, neutral and beneficial mutations. It conditions the evolutionary trajectory of populations, as well as the rate of adaptive molecular evolution (). Inference of DFE and from patterns of polymorphism (SFS) and divergence data has been a longstanding goal of evolutionary genetics. A widespread assumption shared by numerous methods developed so far to infer DFE and from such data is that beneficial mutations contribute only negligibly to the polymorphism data. Hence, a DFE comprising only deleterious mutations tends to be estimated from SFS data, and is only predicted by contrasting the SFS with divergence data from an outgroup. Here, we develop a hierarchical probabilistic framework that extends on previous methods and also can infer DFE and from polymorphism data alone. We use extensive simulations to examine the performance of our method. We show that both a full DFE, comprising both deleterious and beneficial mutations, and can be inferred without resorting to divergence data. We demonstrate that inference of DFE from polymorphism data alone can in fact provide more reliable estimates, as it does not rely on strong assumptions about a shared DFE between the outgroup and ingroup species used to obtain the SFS and divergence data. We also show that not accounting for the contribution of beneficial mutations to polymorphism data leads to substantially biased estimates of the DFE and . We illustrate these points using our newly developed framework, while also comparing to one of the most widely used inference methods available.

Evolutionary Biology

Regmex, Motif analysis in ranked lists of sequences

Motif analysis has long been an important method to characterize biological functionality and the current growth of sequencing-based genomics experiments further extends its potential. These diverse experiments often generate sequence lists ranked by some functional property. There is therefore a growing need for motif analysis methods that can exploit this coupled data structure and be tailored for specific biological questions. Here, we present a motif analysis tool, Regmex (REGular expression Motif EXplorer), which offers several methods to identify overrepresented motifs in a ranked list of sequences. Regmex uses regular expressions to define motifs or families of motifs and embedded Markov models to calculate exact probabilities for motif observations in sequences. Motif enrichment is optionally evaluated using random walks, Brownian bridges, or modified rank based statistics. These features make Regmex well suited for a range of biological sequence analysis problems related to motif discovery. We demonstrate different usage scenarios including rank correlation of microRNA binding sites co-occurring with a U-rich motif. The method is available as an R package.

Bioinformatics

Inference under a Wright-Fisher model using an accurate beta approximation

The large amount and high quality of genomic data available today enables, in principle, accurate inference of evolutionary history of observed populations. The Wright-Fisher model is one of the most widely used models for this purpose. It describes the stochastic behavior in time of allele frequencies and the influence of evolutionary pressures, such as mutation and selection. Despite its simple mathematical formulation, exact results for the distribution of allele frequency (DAF) as a function of time are not available in closed analytic form. Existing approximations build on the computationally intensive diffusion limit, or rely on matching moments of the DAF. One of the moment-based approximations relies on the beta distribution, which can accurately describe the DAF when the allele frequency is not close to the boundaries (zero and one). Nonetheless, under a Wright-Fisher model, the probability of being on the boundary can be positive, corresponding to the allele being either lost or fixed. Here, we introduce the beta with spikes, an extension of the beta approximation, which explicitly models the loss and fixation probabilities as two spikes at the boundaries. We show that the addition of spikes greatly improves the quality of the approximation. We additionally illustrate, using both simulated and real data, how the beta with spikes can be used for inference of divergence times between populations, with comparable performance to existing state-of-the-art method.

Bioinformatics

diCal-IBD: demography-aware inference of identity-by-descent tracts in unrelated individuals

Summary: We present a tool, diCal-IBD, for detecting identity-by-descent (IBD) tracts between pairs of genomic sequences. Our method builds on a recent demographic inference method based on the coalescent with recombination, and is able to incorporate demographic information as a prior. Simulation study shows that diCal-IBD has significantly higher recall and precision than that of existing IBD detection methods, while retaining reasonable accuracy for IBD tracts as small as 0.1 cM.\n\nAvailability: http://sourceforge.net/p/dical-ibd\n\nContact: yss@eecs.berkeley.edu

Bioinformatics