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Rapid Genomic Sequencing in the NICU: Supporting Care Decisions, Workflows, and Families
As genomic testing becomes more integrated into neonatal care, NICU teams play an important role in helping patients and families navigate complex clinical journeys. This webinar will explore practical applications of rapid genome sequencing in the NICU and discuss how earlier genetic insights can influence care coordination, interdisciplinary workflows, and family communication.
Kiley Moran
BSN, MBE
I’m a healthcare strategist, former NICU nurse, and bioethicist with a career rooted in improving care for women, children, and families. I began my career in pediatric and neonatal critical care before transitioning into medical education, business development, and commercial leadership across maternal-fetal health technologies, medical devices, and biotechnology. My work has evolved from supporting clinicians at the bedside to leading national growth and commercialization strategies in precision medicine and genomics, with a focus on expanding access to innovative technologies and driving meaningful change in clinical practice. I completed graduate training in bioethics at Harvard Medical School, further shaping my interest in clinical ethics, health equity, and the responsible integration of emerging technologies into healthcare. I’m currently pursuing a Doctor of Public Health (DrPH) to build on this work at the intersection of clinical care, healthcare innovation, and public health.
Related webinars
In pediatric critical care settings, patients may present with complex symptoms that do not point to a clear diagnosis. This webinar follows real, anonymized patient cases where ultraRapid genome sequencing helped uncover genomic answers in 48 hours.
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