ESHG Workshop 2012

Wednesday 15 April 2015
Applications:
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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.

Find out more about about OGT's array-based clinical genetics products and sequencing services.