Graham Gower

Graham Gower

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Graham Gower

Section for Molecular Ecology and Evolution, Globe Institute, University of Copenhagen , Copenhagen

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 December 2021 in Genetics
Verified
Journal Article
Open access
PDF file
FBFranz Baumdicker
Franz Baumdicker
GBGertjan Bisschop
Gertjan Bisschop
DGDaniel Goldstein
Daniel Goldstein
GGGraham Gower
Graham Gower
ARAaron P Ragsdale
Aaron P Ragsdale
JKJerome Kelleher
Jerome Kelleher
Stochastic simulation is a key tool in population genetics, since the models involved are often analytically intractable and simulation is usually the only way of obtaining ground-truth data to evaluate inferences. Because of this, a large number of specialized simulation programs have been developed, each filling a particular niche, but with largely overlapping functionality and a substantial duplication of effort. Here, we introduce msprime version 1.0, which efficiently implements ancestry and mutation simulations based on the succinct tree sequence data structure and the tskit library. We summarize msprime’s many features, and show that its performance is excellent, often many times faster and more memory efficient than specialized alternatives. These high-performance features have been thoroughly tested and validated, and built using a collaborative, open source development model, which reduces duplication of effort and promotes software quality via community engagement.

23 June 2020 in eLife
Verified
Journal Article
Open access
JAJeffrey R Adrion
Jeffrey R Adrion
CCChristopher B Cole
Christopher B Cole
NDNoah Dukler
Noah Dukler
JGJared G Galloway
Jared G Galloway
AGAriella L Gladstein
Ariella L Gladstein
AKAndrew D Kern
Andrew D Kern
The explosion in population genomic data demands ever more complex modes of analysis, and increasingly, these analyses depend on sophisticated simulations. Recent advances in population genetic simulation have made it possible to simulate large and complex models, but specifying such models for a particular simulation engine remains a difficult and error-prone task. Computational genetics researchers currently re-implement simulation models independently, leading to inconsistency and duplication of effort. This situation presents a major barrier to empirical researchers seeking to use simulations for power analyses of upcoming studies or sanity checks on existing genomic data. Population genetics, as a field, also lacks standard benchmarks by which new tools for inference might be measured. Here, we describe a new resource, stdpopsim, that attempts to rectify this situation. Stdpopsim is a community-driven open source project, which provides easy access to a growing catalog of published simulation models from a range of organisms and supports multiple simulation engine backends. This resource is available as a well-documented python library with a simple command-line interface. We share some examples demonstrating how stdpopsim can be used to systematically compare demographic inference methods, and we encourage a broader community of developers to contribute to this growing resource.

25 May 2021 in eLife
Verified
Journal Article
Open access
GGGraham Gower
Graham Gower
PPPablo Iáñez Picazo
Pablo Iáñez Picazo
MFMatteo Fumagalli
Matteo Fumagalli
FRFernando Racimo
Fernando Racimo
Studies in a variety of species have shown evidence for positively selected variants introduced into a population via introgression from another, distantly related population—a process known as adaptive introgression. However, there are few explicit frameworks for jointly modelling introgression and positive selection, in order to detect these variants using genomic sequence data. Here, we develop an approach based on convolutional neural networks (CNNs). CNNs do not require the specification of an analytical model of allele frequency dynamics and have outperformed alternative methods for classification and parameter estimation tasks in various areas of population genetics. Thus, they are potentially well suited to the identification of adaptive introgression. Using simulations, we trained CNNs on genotype matrices derived from genomes sampled from the donor population, the recipient population and a related non-introgressed population, in order to distinguish regions of the genome evolving under adaptive introgression from those evolving neutrally or experiencing selective sweeps. Our CNN architecture exhibits 95% accuracy on simulated data, even when the genomes are unphased, and accuracy decreases only moderately in the presence of heterosis. As a proof of concept, we applied our trained CNNs to human genomic datasets—both phased and unphased—to detect candidates for adaptive introgression that shaped our evolutionary history.

11 December 2017 in Nature Ecology & Evolution
Verified
Journal Article
Open access
PDF file
CFCharles Feigin
Charles Feigin
ANAxel Newton
Axel Newton
LDLiliya Doronina
Liliya Doronina
JSJürgen Schmitz
Jürgen Schmitz
CHChristy A. Hipsley
Christy A. Hipsley
APAndrew Pask
Andrew Pask
The Tasmanian tiger or thylacine (Thylacinus cynocephalus) was the largest carnivorous Australian marsupial to survive into the modern era. Despite last sharing a common ancestor with the eutherian canids ~160 million years ago, their phenotypic resemblance is considered the most striking example of convergent evolution in mammals. The last known thylacine died in captivity in 1936 and many aspects of the evolutionary history of this unique marsupial apex predator remain unknown. Here we have sequenced the genome of a preserved thylacine pouch young specimen to clarify the phylogenetic position of the thylacine within the carnivorous marsupials, reconstruct its historical demography and examine the genetic basis of its convergence with canids. Retroposon insertion patterns placed the thylacine as the basal lineage in Dasyuromorphia and suggest incomplete lineage sorting in early dasyuromorphs. Demographic analysis indicated a long-term decline in genetic diversity starting well before the arrival of humans in Australia. In spite of their extraordinary phenotypic convergence, comparative genomic analyses demonstrated that amino acid homoplasies between the thylacine and canids are largely consistent with neutral evolution. Furthermore, the genes and pathways targeted by positive selection differ markedly between these species. Together, these findings support models of adaptive convergence driven primarily bycis-regulatory evolution.

18 October 2016 in Nature Communications
Verified
Journal Article
Open access
JSJulien Soubrier
Julien Soubrier
GGGraham Gower
Graham Gower
Kefei ChenKefei Chen
Kefei Chen
SRStephen M. Richards
Stephen M. Richards
Bastien LlamasBastien Llamas
Bastien Llamas
ACAlan Cooper
Alan Cooper
The two living species of bison (European and American) are among the few terrestrial megafauna to have survived the late Pleistocene extinctions. Despite the extensive bovid fossil record in Eurasia, the evolutionary history of the European bison (or wisent,Bison bonasus) before the Holocene (<11.7 thousand years ago (kya)) remains a mystery. We use complete ancient mitochondrial genomes and genome-wide nuclear DNA surveys to reveal that the wisent is the product of hybridization between the extinct steppe bison (Bison priscus) and ancestors of modern cattle (aurochs,Bos primigenius) before 120 kya, and contains up to 10% aurochs genomic ancestry. Although undetected within the fossil record, ancestors of the wisent have alternated ecological dominance with steppe bison in association with major environmental shifts since at least 55 kya. Early cave artists recorded distinct morphological forms consistent with these replacement events, around the Last Glacial Maximum (LGM, ∼21–18 kya).

13 January 2021 in Nature
Verified
Journal Article
Closed access
PDF file
APAngela R. Perri
Angela R. Perri
Kieren J. MitchellKieren J. Mitchell
Kieren J. Mitchell
AMAlice Mouton
Alice Mouton
SÁSandra Álvarez-Carretero
Sandra Álvarez-Carretero
AHArdern Hulme-Beaman
Ardern Hulme-Beaman
LFLaurent A. F. Frantz
Laurent A. F. Frantz