Genetic diversity on the human X chromosome does not support a strict pseudoautosomal boundary

Genetic diversity on the human X chromosome does not support a strict pseudoautosomal boundary

Daniel J Cotter, Sarah M Brotman, Melissa A Wilson Sayres

Modeling Continuous Admixture

Modeling Continuous Admixture

Ying Zhou, Hongxiang Qiu, Shuhua Xu

Archaic adaptive introgression in TBX15/WARS2

Archaic adaptive introgression in TBX15/WARS2

Fernando Racimo, David Gokhman, Matteo Fumagalli, Torben Hansen, Ida Moltke, Anders Albrechtsen, Liran Carmel, Emilia Huerta-Sanchez, Rasmus Nielsen

Low virulence evolves as a bet-hedging strategy in fluctuating environment

Low virulence evolves as a bet-hedging strategy in fluctuating environment

Anne Nguyen, Etienne Rajon, David Fouchet, Dominique Pontier, Jorge Rabinovich, Sebastien Gourbiere, Frederic Menu

The impact of natural selection on the distribution of cis-regulatory variation across the genome of an outcrossing plant

The impact of natural selection on the distribution of cis-regulatory variation across the genome of an outcrossing plant

Kim A Steige, Benjamin Laenen, Johan Reimegård, Douglas Scofield, Tanja Slotte

Stochastic modelling, Bayesian inference, and new in vivo measurements elucidate the debated mtDNA bottleneck mechanism

Stochastic modelling, Bayesian inference, and new in vivo measurements elucidate the debated mtDNA bottleneck mechanism
Iain G. Johnston, Joerg P. Burgstaller, Vitezslav Havlicek, Thomas Kolbe, Thomas Rulicke, Gottfried Brem, Jo Poulton, Nick S. Jones

Dangerous damage to mitochondrial DNA (mtDNA) can be ameliorated during mammalian development through a highly debated mechanism called the mtDNA bottleneck. Uncertainty surrounding this process limits our ability to address inherited mtDNA diseases. We produce a new, physically motivated, generalisable theoretical model for mtDNA populations during development, allowing the first statistical comparison of proposed bottleneck mechanisms. Using approximate Bayesian computation and mouse data, we find most statistical support for a combination of binomial partitioning of mtDNAs at cell divisions and random mtDNA turnover, meaning that the debated exact magnitude of mtDNA copy number depletion is flexible. New experimental measurements from a wild-derived mtDNA pairing in mice confirm the theoretical predictions of this model. We analytically solve a mathematical description of this mechanism, computing probabilities of mtDNA disease onset, efficacy of clinical sampling strategies, and effects of potential dynamic interventions, thus developing a quantitative and experimentally-supported stochastic theory of the bottleneck.

The Equidistance Index of Population Structure

The Equidistance Index of Population Structure

Yaron Granot, Saharon Rosset, Karl Skorecki

Fitness effects of new mutations in Chlamydomonas reinhardtii across two stress gradients

Fitness effects of new mutations in Chlamydomonas reinhardtii across two stress gradients

Susanne A Kraemer, Andrew D Morgan, Robert W Ness, Peter D Keightley, Nick Colegrave

Evolution arrests invasions of cooperative populations

Evolution arrests invasions of cooperative populations

Kirill S Korolev

A Bayesian test to identify variance effects

A Bayesian test to identify variance effects
Bianca Dumitrascu, Gregory Darnell, Julien Ayroles, Barbara E Engelhardt

Identifying genetic variants that regulate quantitative traits, or QTLs, is the primary focus of the field of statistical genetics. Most current methods are limited to identifying mean effects, or associations between genotype and the mean value of a quantitative trait. It is possible, however, that a genetic variant may affect the variance of the quantitative trait in lieu of, or in addition to, affecting the trait mean. Here, we develop a general methodological approach to identifying covariates with variance effects on a quantitative trait using a Bayesian heteroskedastic linear regression model. We show that our Bayesian test for heteroskedasticity (BTH) outperforms classical tests for differences in variation across a large range of simulations drawn from scenarios common to the analysis of quantitative traits. We apply BTH to methylation QTL study data and expression QTL study data to identify variance QTLs. When compared with three tests for heteroskedasticity used in genomics, we illustrate the benefits of using our approach, including avoiding overfitting by incorporating uncertainty and flexibly identifying heteroskedastic effects.