The Office of Public Health Genomics (OPHG) provides updated and credible information on how genomic
information and family health history can improve health and influence policy and practice. We highlight
news and information on the use of genomic tests and other applications, including family health history,
in clinical and public health practice and programs, along with relevant data, policy, and legislation. We hope the update is informative to practitioners, policy makers, consumers, and researchers. Please send
your comments to: genetics@cdc.gov.
Public Health Sciences
- Getting ready for the human phenome project: The 2012 Forum of the Human Variome Project
Oetting WS, et al. Hum Mutat 2013 Feb - HDAM: a resource of human disease associated mutations from next generation sequencing studies
Jia M, et al. BMC Med Genomics 2013;6 Suppl 1:S16 - MRSA transmission on a neonatal intensive care unit: Epidemiological and genome-based phylogenetic analyses
Ulrich Nübel et al. PloS One 2013 Jan 31
- Whole genome sequencing versus traditional genotyping for investigation of a mycobacterium tuberculosis outbreak: A longitudinal molecular epidemiological study
Andreas Roetzer et al. PLoS Medicine Feb 2013
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