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The US Preventive Services Task Force is calling for more research on screening for lipid disorders in children and adolescents before it recommends universal testing.
Advances in understanding the diverse genetic causes of childhood-onset hearing loss suggest that genomic testing could help with treatment planning, including appropriate therapy timing.
UK patients will benefit from a new partnership with Thailand to share expertise of genome sequencing, collaborate in research, education and training opportunities, knowledge exchange and genomics data handling.
Advances in understanding the many different genetic causes of childhood-onset hearing loss indicate that genomic testing could assist in treatment planning, including optimal timing of treatment.
Announcing a new article publication for Zoonoses journal. The monkeypox outbreaks started in 2022 and became an unexpected public health emergency of international concern (PHEIC).
Researchers from Nigeria and the United Kingdom (U.K.) analyzed mpox virus genomes and found that divergent lineages of the mpox virus exhibiting human-to-human transmission existed in the Nigerian population before the 2022 spread of the virus outside of the endemic regions.
help prepare them to be the ones who actually do that verification of these negative covid tests. >> josh lederman live on the white house north lawn, thank you for that reporting. dr. gupta, let me go to you here. is this the right call by the administration? >> absolutely. this is proactive. as josh has already said, this is meant to slow transmission, not eliminate it. we're dealing with variants here in the united states, xvp being the newest incarnation. this isn't about eliminating new variants of concern, but about having surveillance, about knowing what we're dealing with so we can potentially buy time to understand if a variant of concern is originating out of the chinese main land or hong kong, that we would be able to see whether or not that variant is susceptible to the vaccine treatments we have. this is about building in intelligence surveillance where it doesn't exist because the chinese are not sharing the genomic data to the global
How can Canada optimize the impact of human genomic sequencing to increase our understanding of disease? New guidance in CMAJ (Canadian Medical Association Journal) lays out the key elements for obtaining patient consent for researchers and policymakers in this growing field.
A new statistical method provides a more efficient way to uncover biologically meaningful changes in genomic data that span multiple conditions -; such as cell types or tissues.