SEQUENOM Signs Research Agreement with Translational Genomics Research Institute
"We are excited about working with SEQUENOM in order to add an extensive clinical genetics component to our melanoma research programs," stated Jeffrey Trent, Ph.D., TGen's President. "We hope this collaboration will result in promising new methods for the diagnosis and treatment of melanoma, the most devastating form of skin cancer that affects over 50,000 people per year in the US alone."
"TGen is a world-leading institution in the area of melanoma research, and we are excited about their commitment to our disease gene portfolio," said Toni Schuh, Ph.D., SEQUENOM's President and Chief Executive Officer. "This collaboration exemplifies SEQUENOM's strategy and efforts to leverage our discovery assets while moving towards profitability."
SEQUENOM has identified more than 60 candidate genes in breast, lung, prostate and skin cancers, central nervous system disorders, metabolic and cardiovascular diseases and musculoskeletal and inflammatory conditions through high-density genome-wide scans using its MassARRAY platform technology. Access to SEQUENOM's high throughput genetic analysis center, combined with SEQUENOM's SNP assay portfolio and DNA sample database, provide SEQUENOM with sufficient leverage to become a significant participant in the clinical research market for the supply of high quality genetic analysis, including clinical genetics and diagnostics for molecular medicine.
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Topic world Diagnostics
Diagnostics is at the heart of modern medicine and forms a crucial interface between research and patient care in the biotech and pharmaceutical industries. It not only enables early detection and monitoring of disease, but also plays a central role in individualized medicine by enabling targeted therapies based on an individual's genetic and molecular signature.
Topic world Diagnostics
Diagnostics is at the heart of modern medicine and forms a crucial interface between research and patient care in the biotech and pharmaceutical industries. It not only enables early detection and monitoring of disease, but also plays a central role in individualized medicine by enabling targeted therapies based on an individual's genetic and molecular signature.