Genetics

Grants Bio-Techne expanded commercial rights to develop a portfolio of genetics products beyond the recently launched AmplideX® Nanopore…

Summary: Scientists have discovered that mutations in the EPG5 gene—known for causing the rare childhood disorder Vici syndrome—also…

Rare hereditary diseases can be identified in patients and specific mutations in tumour cells detected – DNA sequencing…

Ochsner Health announces the launch of its Genetic Wellness Assessment, an innovative screening tool to help identify individuals…

Researchers at Cleveland Clinic Children’s have helped identify a previously unknown gene that increases the risk of developing…

Conventional genetic analysis methods for genotyping of brain tumors usually require one or two days to obtain results…

A research team in Japan has developed an innovative system that can accurately detect genetic mutations in the…

Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis…

Rare hereditary diseases can be identified in patients and specific mutations in tumour cells detected – DNA sequencing…

Researchers from the University of Exeter and ULB have identified mutations in the TMEM167A gene causing a rare…

The prevalence of Alzheimer disease (AD) is approximately two times higher in African Americans (AA) compared to White/European-ancestry…

In a groundbreaking study detailed in the latest issue of The Crop Journal, scientists from Shandong Agricultural University…

Bio-Techne and Oxford Nanopore Technologies Expand Agreement to Accelerate Development of Genetics Portfolio Through 2032