Sign up: SMBE Satellite Mtg. on Eukaryotic-Omics 4/29-5/2 at #UCDavis

Going to be good:

Eukaryotes | SMBE Satellite Meeting on Eukaryotic -Omics - April 29 to May 2, UC Davis Conference Center

No bias here - given that it is organized by Holly Bik in my lab and it is at UC Davis. The lineup of speakers is great and the topic is timely.  So sign up  ...

Speakers:

Rachel AdamsUC BerkeleyGroundtruthing next-gen sequencing for microbial ecology: is beta diversity robust to errors in pyrosequencing?
Nicholas A. BokulichUC DavisRegional Patterns in Grape Fungal Consortia Define Wine Fermentation Communities
Sara BrancoUC BerkeleyFungi at a small-scale: spatial zonation of fungal assemblages around single trees
C. Titus BrownMichigan State UniversitySequencing and assembly of diverse eukaryotes: like metagenomics, but much harder
Peter CountwayBigelow Laboratory for Ocean SciencesTitle TBA
Simon CreerBangor University, WalesTitle TBA
Tom DelmontMarine Biological Laboratory, Woods HolePhaeocystis antarctica spatiotemporal diversity, activity and its relation to prokaryotes and viruses using physiological and ‘omic approaches
Jonathan EisenUC DavisThe need for a phylogeny driven genomic encyclopedia of eukaryotes
Laura EmeDalhousie UniversityLarge scale phylogenomic analyses of Blastocystis subtype 1 reveals a major role for lateral gene transfer in adaptation to parasitism of the human gut
Jack GilbertArgonne National LabAddressing microbial eukaryotic biogeography in home, hospitals and the world
Jean-David GrattepancheSmith CollegeTitle TBA
Victor Hanson-SmithUC San FranciscoIdentifying Loci of Functional Evolution in Ancestral Genes
Ian KingUniversity of GuelphBiomonitoring 2.0: A high-throughput genomics approach for comprehensive biological assessment of environmental change
Andrew KrohnNorthern Arizona UniversityRhizosphere microbial community dynamics of drought-stressed pinyon pines (Poster)
Franck LejzerowiczUniversity of GenevaExploring the deep-sea foraminiferal diversity by multiplexed RNA and DNA-based ultra-deep sequencing and ultra-fast bioinformatic analyses
Matthew MorganCSIRO AustraliaNext-generation sequencing reveals the impacts of inundation and drought on eukaryote biodiversity in semi-arid floodplain soils
Laura Wegener ParfreyUniversity of Colorado, BoulderIncorporating microbial eukaryotes into analyses of the human microbiome
Katherine PollardUC San FranciscoTitle TBA
Dorota PorazinskaUniversity of FloridaDiscrimination of microscopic pests of agricultural importance with NGS
Thomas RichardsNHM LondonTitle TBA
Surya SahaCornell UniversityComposition of the Maize Endophytic Microbiome is Correlated with Maize Genotype (Poster)
Søren SørensenUniversity of CopenhagenTitle TBA
Fabian StaubachStanford UniversityHost species and environmental effects on bacterial communities associated with Drosophila in the laboratory and in the natural environment
Sarah StephensonCSIRO AustraliaMetagenetic examinations of benthic eukaryl estuarine communities
Joshua SternGeorgia Institute of TechnologySearching for the Phylogenetic Place of Eukaryotes, Using Data from STORI
W. Kelley ThomasUniversity of New HampshireTitle TBA
Xianfa XieVirginia State UniversityComparative genomic study of the origin and evolution of eukaryotes

SMBE 2012: Microbial Genome Evolution Symposium

Along with my colleagues Xavier Didelot, Ed Feil, Eduardo Rocha and Howard Ochman, I will be organizing a symposium on Microbial Genome Evolution at the 2012 meeting of the Society for Molecular Biology and Evolution in Dublin, Ireland. The deadline for abstract submission is 27th January 2012. This is the synopsis for our symposium:
High-throughput sequencing makes it possible for the first time to sequence hundreds of microbial genomes rapidly at low cost. These methods have huge potential to significantly improve our understanding of microbial evolution, so that many research projects have recently been set up to generate and analyze such data. This symposium will provide an overview of the progress made by such projects, as well as the many challenges they pose. It is now possible to identify the vast majority of SNPs within large population samples of microbial isolates. These datasets are illuminating the molecular, ecological and population-level dynamic processes occurring over short time scales in natural populations inhabiting a range of habitats from the clinic to the environment. We aim to  explore these recent advances and the development of new methods of analyses required to fully exploit these extremely large sequence datasets. Relevant topics include quantifying the variation in the rates of recombination and mutation between closely related lineages, the evolution of base composition, the relative power of drift and selection, examining the acquisition of adaptive traits (e.g. antibiotic resistance, host adaptation, metabolic flexibility, regulatory changes) within a phylogenetic framework, and the distribution of variation over time and space (phylogeography). The role of phage and conjugative elements in structuring populations as both vehicles for gene flow and parasitic elements will also be considered. The symposium will focus on variation within natural populations rather than experimental evolution.

What are the conditions for multiple foci of adaptation?

Selection on standing variation, soft sweeps, parallel adaptation: these alternatives to the population genetics paradigm of the S-shaped selective sweep have in common the idea that the response of a species to a change in selection pressure may frequently involve multiple mutations, which may arise in multiple locales, and which may appear at different sites in the genome. Consequently, the footprint of selection in the genome is different to that expected under a single selective sweep and therefore likely to be missed by scans of the genome looking for selection.

Many examples of parallel adaptation have been put forward, for instance multiple drug resistance in the malaria parasite Plasmodium vivax. But how plausible is parallel adaptation as an evolutionary mechanism, and what are the conditions that make it likely? These questions were addressed by Graham Coop presenting joint work with his postdoc Peter Ralph in one of the stand-out talks of the SMBE conference in Lyon.

Their key finding is that the multifarious parameters that go into building a spatial model of adaptation (strength of selection, the mutation rate, population density, average dispersal distance of offspring) can be distilled down to a single key quantity: the characteristic length given by the equation
When the geographical extent of the species range exceeds this characteristic length, the conditions are right for parallel adaptation. Graham's talk made accessible the complex mathematics behind this result. He has kindly made the slides available (click here) and the paper is now available at the Genetics website (click here).

Discovering the distribution of fitness effects

At this year's Society for Molecular Biology and Evolution meeting in Lyon I presented ongoing work estimating the distribution of fitness effects, which is a collaborative venture with Molly Przeworski and Peter Andolfatto. Earlier versions of this research appeared in talks I presented at Chicago in December (Ecology and Evolution Departmental seminar) and Liverpool in January (UK Population Genetics Group meeting), and it follows on from last year's SMBE presentation in which I discussed methods to tease out sub-genic variation in selection pressure.

There is intrinsic interest in the fitness effects of novel mutations in coding regions of the genome, especially the relative frequency of occurrence of neutral, beneficial and deleterious variants. Yet estimating the distribution of fitness effects (the DFE) is also of practical use when localizing the signal of adaptive evolution. The reason is that in Bayesian analyses, the assumed DFE can influence the strength of evidence for or against adaptation at a particular site. Consequently it is preferably to estimate the DFE at the same time as detecting adaptation at individual sites to avoid prior assumptions unduly influencing the results.

Having estimated the DFE, it is of use in quantifying the relative contribution of adaptation versus drift to genome evolution. The figure, taken from my talk in Lyon (slides here), illustrates the idea when a normal distribution is used to estimate the DFE; the relative area of the green to the yellow shaded regions represents the respective contribution of adaptation versus drift in amino acid substitutions accrued along the Drosophila melanogaster lineage.

omegaMap at BioHPC

All evolutionary biologists wishing to make use of omegaMap now have access to a high performance parallel computing cluster via the internet courtesy of Cornell's CBSU and Microsoft. The software, which allows the detection of selection and recombination in DNA or RNA sequences, can be run via the web interface at cbsuapps.tc.cornell.edu/omegamap.aspx, or downloaded as part of the BioHPC suite.

The web interface consists of a simple form where users can upload their configuration file and sequences in FASTA format. Completed jobs are notified by e-mail. To learn more about the project visit the CBSU home page.

Meanwhile, I am working on several major updates to omegaMap, the most interesting of which will probably be the development of a new model that allows for the joint analysis of natural selection acting on sequences from different populations or species. The aim is to integrate population genetic and phylogenetic models of selection in order to exploit the signal of selection contained both in polymorphism within populations (or species) and divergence between them. I will be presenting progress on this work, in the context of hominid evolution, at the 2009 SMBE meeting in Iowa City this June.