Welcome to our lab! The Paleogenomics Lab is a joint venture between two PIs: Beth Shapiro, and Richard (Ed) Green (see Ed's lab website in BME). Our research focuses on a wide range of evolutionary and ecological questions, mostly involving the application of genomics techniques to better understand how species and populations evolve through time.
Our groups incorporate experimental and computational approaches. We generate new data and devise new approaches to their analysis, such as tools to assemble genomes and to analyze genomic and population genetic data. Our interests are broad, spanning human evolution, genome assembly and analysis, pathogen evolution, population genetics, conservation genomics, and the genomic consequences of long-term environmental change.
mammoth tusk emerging from permafrost near Dawson City, YT, Canada
In the Shapiro lab, a common theme to our research is that it tends to involve some aspect of time. The temporal signal comes from historical information, radiocarbon dates, sampling times (for rapidly evolving viruses), or information from depositional environments. (Check us out in the field!) We combine temporal and genetic data to identify periods of growth, decline, dispersal, and replacement in populations. When possible, we integrate these data with climate and environmental records to try to identify the causative factors behind changes in genetic diversity.
We tend to us either a multi-locus approach, in which we enrich our ancient samples for particular loci of interest, or complete genome, data... even for our oldest samples!
We have a strong interest in linking genomic data from the past to genomic data isolated from living populations so as to inform decisions that relate to the protection and management of species that are alive today.
In the Green lab, we are interested in genome biology. We are particularly focused on the problems of assembly and comparative genome analysis. Recent and ongoing projects include genome-scale analysis of archaic human genome sequence, comparative genomics of Crocodilia, and the development of new methods to assemble high quality de novo genomes. We are also interested in applying high-throughput sequencing to address questions in molecular biology including the evolution of gene expression, alternative splicing, and population genetics.
The discovery that DNA could be extracted and characterised from preserved biological remains motivated an entirely new field in moleular evolution. Using DNA sequences, or even complete genomes, recovered from these remains, it was possible to trace molecular evolutionary processes in species and populations through time, actually watching evolution as it happens. Using DNA techniques coupled with next-generation sequencing technologies, we aim to answer questions such as:
How does genetic diversity change in response to environmental changes?
How frequent are local extinctions, population replacements and migration, and how do these affect our ability to infer evolutionary history?
How can we use genetic data from the past to predict species' responses to future climate change?