Genetic Sequencers
Brigham Genomic Medicine brings together scientists and clinicians to diagnose, discover genetic underpinnings of disease, and shape treatment
Molecular profiling of tumors is opening novel therapeutic avenues
New report recommends minimum of 34 critical gene inclusions for high-throughput pan-myeloid sequencing tests to help standardize clinical practice and improve patient care
Hastings Center Report, co-edited by UCSF bioethicist, outlines ethics and policy recommendations on genome-wide sequencing of newborns
Powerful, flexible, and easy-to-use analysis solution gets the most out of NGS data
FOXP2, a gene implicated in affecting speech and language, is held up as a textbook example of positive selection on a human-specific trait
Currently, detecting and subtyping foodborne pathogens are separate processes, but UGA scientist Xiangyu Deng has combined these two steps through a process called “metagenomics analysis”
New research highlights that the evolution of these extraordinary animals and other rorquals was also anything but ordinary
To date, gene expression in tumors has been typically profiled by capturing messenger RNAs; however, they represent only a fraction of the molecules detected
