We have developed a computational Grid that enables us to exploit through a single interface a range of local, national and international resources. It insulates the user as far as possible from issues concerning administrative boundaries, passwords and different operating system features. This work has been undertaken as part of the European Union ImmunoGrid project whose aim is to develop simulations of the immune system at the molecular, cellular and organ levels. The ImmunoGrid consortium has members with computational resources on both sides of the Atlantic. By making extensive use of existing Grid middleware, our Grid has enabled us to exploit consortium and publicly available computers in a unified way, notwithstanding the diverse local software and administrative environments. We took 40 000 polypeptide sequences from 4000 avian and mammalian influenza strains and used a neural network for class I T-cell epitope prediction tools for 120 class I alleles and haplotypes to generate over 14 million high-quality protein–peptide binding predictions that we are mapping onto the three-dimensional structures of the proteins. By contrast, the Grid is also being used for developing new methods for class T-cell epitope predictions, where we have running batches of 120 molecular dynamics free-energy calculations.
One contribution of 16 to a Theme Issue ‘Crossing boundaries: computational science, e-Science and global e-Infrastructure II. Selected papers from the UK e-Science All Hands Meeting 2008’.
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