What we do
The Computational Oncogenomics Group works on the computational analysis of structural genome variations in cancer, centred around our arrayMap and Progenetix resources of curated molecular-cytogenetic and sequencing data.
Specific projects explore computational methods, genomics of selected tumour entities and genomic variation patterns across malignancies and populations.
As members of the Global Alliance for Genomics and Health, the group is developing standards in biocuration and data sharing for genomic variants and phenotypic data. Other projects are related to genome data epistemology, e.g. geographic and diagnostic sampling bias.
Find out more about the Group’s activities
Main publication 2019
- Saunders G et al.
European infrastructures to access one million human genomes by 2022
Nature Reviews Genetics, https://doi.org/10.1038/s41576-019-0156-9 - Fiume M et al.
Federated discovery and sharing of genomic data using Beacons
Nat Biotechnol, https://doi.org/10.1038/s41587-019-0046-x - Gug G et al.
DNA copy number imbalances in primary cutaneous lymphomas (PCL)
JEADV, https://doi.org/10.1111/jdv.15442
