Skip to main content
Premium Trial:

Request an Annual Quote

Ray Wu, Bard Geesaman, Julie Golden

Ray Wu, a professor of molecular biology and genetics at Cornell University, died last week at the age of 79. According to Cornell’s College of Agriculture and Life Sciences, Wu in 1970 developed the first method for sequencing DNA, as well as fundamental tools for DNA cloning. He joined the Cornell faculty in 1966. Born in Beijing in 1928, Wu came to the US in 1948, where he earned a bachelor’s degree in chemistry from the University of Alabama, Tuscaloosa, and a doctoral degree in biochemistry from the University of Pennsylvania.

Bard Geesaman has become executive director of life sciences of the X Prize Foundation, where he will be responsible for developing, funding, and running new prizes in the area of life sciences, which will include cancer, healthcare, and genomics prizes. The foundation intends to launch 10 to 15 new prizes, worth $300 million, over the next seven years, several of which will be in the life sciences. Geesaman comes to the X Prize Foundation from MPM Capital, where he worked as a venture partner. He holds a PhD in systems and computational neurobiology from the Massachusetts Institute of Technology, an MD from Harvard Medical School, and a BS in systems neurobiology from the University of California, Berkeley.

Julie Golden has become technical leader for the forensic processing laboratory of DNA Security. She has served as a senior forensic DNA analyst and QA officer for a government crime laboratory, a forensic DNA auditor, and as a CODIS consultant to several government crime laboratories.

The Scan

Genetic Tests Lead to Potential Prognostic Variants in Dutch Children With Dilated Cardiomyopathy

Researchers in Circulation: Genomic and Precision Medicine found that the presence of pathogenic or likely pathogenic variants was linked to increased risk of death and poorer outcomes in children with pediatric dilated cardiomyopathy.

Fragile X Syndrome Mutations Found With Comprehensive Testing Method

Researchers in Clinical Chemistry found fragile X syndrome expansions and other FMR1 mutations with ties to the intellectual disability condition using a long-range PCR and long-read sequencing approach.

Team Presents Strategy for Speedy Species Detection in Metagenomic Sequence Data

A computational approach presented in PLOS Computational Biology produced fewer false-positive species identifications in simulated and authentic metagenomic sequences.

Genetic Risk Factors for Hypertension Can Help Identify Those at Risk for Cardiovascular Disease

Genetically predicted high blood pressure risk is also associated with increased cardiovascular disease risk, a new JAMA Cardiology study says.