The Emphasis on COVID-19-Related Research Biorepository collects, processes, and archives biospecimens from both residual clinical samples and prospective participants with SARS-CoV2 infection. Recruitment and sample collection efforts have been centralized in order to minimize staff exposure, reduce burden on patients and their families, conserve PPE, and facilitate timely and equitable access to samples for researchers.
The COVID-19 Biorepository provides faculty with valuable opportunities for understanding the effects of and response to SARS-CoV2 infection, COVID-19 mechanisms of disease, and virus epidemiology, among other biomedical insights, all of which can improve outcomes for infected individuals, and public health overall.
We are currently collecting plasma, serum, and whole cells (buffy coat) on a daily basis, and have collected thousands of residual serum and plasma samples from clinical blood draws. Samples are dependent on availability and sample types are evolving. We are currently working on processes to collect fresh samples (less than 4 hours post collection) and convalescent samples. To view a current inventory of what is available view the CBR Inventory (updated weekly) and DataDirect.
How to Access to Samples
- Submit a UMOR COVID-related Research Prioritization form
- Submit an IRB application
- After UMOR priority designation and IRB approval, Principal Investigators are expected to review and/or complete:
- Once the above documents have been received and reviewed, and investigators will receive communication via email regarding sample availability and pickup details. In general, samples are intended to be distributed from the MCRU laboratory on the first floor of the Frankel Cardiovascular Center (CVC) on Tuesday and Thursday of each week.
The samples will be archived using LabVantage and will be stored in MCRU for the first few months. These will later be transferred to the CBR for long term storage, and the CBR will process future requests. Notifications will go out in advance regarding the transition of the samples to the CBR.
Interactive Guide for COVID-19 Research
View the COVID-19 Principal Investigator Workflow below for a step-by-step guide to start clinical studies requiring samples, interventional clinical trials, or data studies.