What comes next?

 Enrolled individuals have their samples tied to other NICU data sources (e.g., Sickbay, EPIC, etc.) to enable easier access and use of samples/data.

 Expand enrollment to parents/siblings/other family members as required for studies.

 Form a Caregiver Advisory Board to help inform biorepository focus and procedures. Board is to include individuals with diverse backgrounds to ensure a variety of perspectives are considered.

 Collection of at least one blood sample on every infant enrolled (focus on transported infants who do not have discarded cord blood available).