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- W4387628785 abstract "Managing care for critically ill newborns is a complex process that requires a comprehensive approach which can include examinations by multiple specialists, imaging studies, and laboratory testing. While rapid whole genome sequencing (rWGS) has many aspects that require optimization for speed and accuracy including candidate identification, sample extraction, sequencing, analysis, reporting, and clinical action planning, it has been shown to have high diagnostic yields that can impact patient care and management. Though factors such as cost, turnaround time, and the availability of expertise need to also be considered when using rWGS in a clinical setting, improvements are consistently being made as new technologies develop and our understanding of genomics grows." @default.
- W4387628785 created "2023-10-14" @default.
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- W4387628785 date "2023-11-01" @default.
- W4387628785 modified "2023-10-15" @default.
- W4387628785 title "Rapid Whole Genome Sequencing in Critically Ill Newborns" @default.
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- W4387628785 doi "https://doi.org/10.1016/j.yamp.2023.08.006" @default.
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