Scientists have used advances in genetics to determine 10 subtypes of breast cancer, each of which has a unique genetic fingerprint that could in the future determine a patient’s tailor-made treatment or cure.

Publications
- A Comprehensive Framework for Prioritising Variants in Exome Sequencing Studies of Mendelian Diseases
- Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population
- Identification of High-Confidence Somatic Mutations in Whole Genome Sequence of Formalin-Fixed Breast Cancer Specimens
- Next-Generation Exome Sequencing of Paediatric Inflammatory Bowel Disease Patients Identifies Rare and Novel Variants in Candidate Genes
- High-Throughput Sequencing of mGluR Signalling Pathway Genes Reveals Enrichment of Rare Variants in Autism

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