For a complete list of publications and working papers, please visit my Google Scholar entry.
See below for links to software developed by the group:
Github - main repository for our recent work
GenoSNP for genotype calling on Illumina SNP genotyping arrays.
QuantiSNP for detecting copy number variants from Illumina SNP genotyping data.
OncoSNP for detecting copy number alterations from heterogeneous tumours using Illumina SNP genotyping data.
OncoSNP-SEQ for detecting copy number alterations from heterogeneous tumours using Illumina or Complete Genomics Whole Genome Sequencing data.
HMM-MDP for Bayesian nonparametric modelling of copy number alterations from array CGH data.
mixlasso for Bayesian nonparametric clustering with variable selection.