Dr Ville Mustonen
Ville develops population genetic theory and computational methods to help find and explain functionally relevant natural variation.
Ville graduated from the Helsinki University of Technology (MSc in EE, with distinction) in 2001 having specialised in computational engineering. During his undergraduate years he worked as a research assistant at the Research Centre for Computational Science and Engineering where he also did his master's thesis on molecular simulations under supervision of Professor Kimmo Kaski.
Ville then moved to Oxford and started his graduate work on statistical physics and molecular simulations at the Rudolf Peierls Centre for Theoretical Physics under supervision of Professor Douglas Abraham. His interest in evolution and DNA sparked during a summer school lecture on 'Biologically Inspired Physics', which covered application of statistical physics to sequence alignment problem.
After completing his doctoral degree (DPhil in Physics, University of Oxford, 2005), he moved to Cologne to work with Professor Michael Lässig on population genetic theory. In Cologne Ville developed new statistical methods for identifying functionally relevant genomic variation and for dissecting the individual contributions of different evolutionary forces for sequence evolution. An unexpected outcome of this work has been a more dynamic picture of molecular evolution where genomes evolve under fitness 'seascapes'.
At the Sanger Institute Ville is developing population genetic methods for using measurements of sequence functionality in conjunction with population sequencing data to help explain natural variation.
Selected Publications
A method to infer positive selection from marker dynamics in an asexual population.
Bioinformatics 2012
Quantifying selection acting on a complex trait using allele frequency time-series data.
Molecular biology and evolution2011
PUBMED: 22114362; DOI: 10.1093/molbev/msr289
Distinguishing driver and passenger mutations in an evolutionary history categorized by interference.
Genetics2011;189;3;989-1000
PUBMED: 21900272; PMC: 3213378; DOI: 10.1534/genetics.111.133975
Germline fitness-based scoring of cancer mutations.
Genetics2011;188;2;383-93
PUBMED: 21441214; PMC: 3122307; DOI: 10.1534/genetics.111.127480
Fitness flux and ubiquity of adaptive evolution.
Proceedings of the National Academy of Sciences of the United States of America2010;107;9;4248-53
PUBMED: 20145113; PMC: 2840135; DOI: 10.1073/pnas.0907953107
From fitness landscapes to seascapes: non-equilibrium dynamics of selection and adaptation.
Trends in genetics : TIG2009;25;3;111-9
PUBMED: 19232770; DOI: 10.1016/j.tig.2009.01.002
Energy-dependent fitness: a quantitative model for the evolution of yeast transcription factor binding sites.
Proceedings of the National Academy of Sciences of the United States of America2008;105;34;12376-81
PUBMED: 18723669; PMC: 2527919; DOI: 10.1073/pnas.0805909105
Molecular evolution under fitness fluctuations.
Physical review letters2008;100;10;108101
PUBMED: 18352233
Adaptations to fluctuating selection in Drosophila.
Proceedings of the National Academy of Sciences of the United States of America2007;104;7;2277-82
PUBMED: 17287357; PMC: 1892984; DOI: 10.1073/pnas.0607105104
Evolutionary population genetics of promoters: predicting binding sites and functional phylogenies.
Proceedings of the National Academy of Sciences of the United States of America2005;102;44;15936-41
PUBMED: 16236723; PMC: 1276062; DOI: 10.1073/pnas.0505537102

