Rapid whole-genome sequencing: a clinical frameshift for acutely ill infants
Discover the real-world impact of rapid whole-genome sequencing (rWGS) for acutely ill infants in this summary of clinical data from The Rady Children’s Institute for Genomic Medicine (RCIGM; CA, USA). Find out how the technological updates driven by academia and industry have been translated into improved diagnosis and care for acutely ill children.
Get all the facts and figures to show:
- The value of whole-genome sequencing data
- Why rWGS as a first-line test improves outcomes
- How rWGS saves time and reduces costs
- Why physicians and families value rWGS
- How to partner with RCIGM for rWGS
Submit Your Research to the F1000Research Genomics & Genetics Gateway
Advance the field of whole-genome studies by publishing your research with the F1000Research Genomics & Genetics Gateway. With trusted publishing, open access, and transparent peer review, your work will meet the highest standards of rigor and integrity while driving innovation in genome analysis, sequencing, and genetic research.
Join a platform that values transparency, openness, and author control. Submit your research today at F1000Research Genomics & Genetics Gateway.