mayo.edu Background Inherited polyneuropathies often go undiagnosed. We investigated whole exome sequencing (WES) in utility to identify the genetic causes of diverse forms of inherited ...

Genetic testing platform PleSSision-Exome, a DNA sequencing system that covers more than 19,000 different genes, could help expand personalized cancer medicine in Japan. Developed by Hiroshi ...

The purpose of this study is to test a new set of technologies called Next Generation Sequencing (NGS) that may help identify possible genetic reasons for your medical condition. NGS is a procedure ...

To diagnose them, clinicians use a standard procedure known as exome sequencing. This involves analysing those segments of ...

The US company said that results from the Alpha-CORRECT trial saw its colon cancer diagnostic Oncodetect achieving a ...

In this study, we performed a case–control genetic association study based on whole-exome sequencing (WES) data in RP. The objective of this study was to identify the genetic risk of rare coding ...

The Patient Access Program aims to address these challenges by increasing access to whole exome sequencing for pediatric epilepsy patients. In addition to helping patients receive a genetic ...

Her research focuses on understanding genetic risk of prostate cancer in multi-ancestry populations, particularly using rare variants captured with whole exome sequencing, genome-wide association ...