ESHG Workshop 2012
ESHG 2012 workshop:
Held at the ESHG 2012 conference in Nuremberg, this workshop featured presentations from international experts in array and sequencing-based cancer and rare disease research, including:
Dr Dan Swan — Senior NGS Computational Biologist at OGT
Identifying causative mutations in rare disease and cancer samples using NGS
Professor Jacqueline Schoumans — Head of the Cancer Cytogenetic Unit in Lausanne University Hospital, Switzerland
CGH +SNP arrays for identification of copy number and copy neutral genomic anomalies in haematological and solid cancers
Read an interview with Professor Schoumans discussing her research and choice of array platform, conducted at ESHG by Justin Petrone for GenomeWeb.