“…9,10 As a result, its levels are then experimentally manipulated, likely inappropriately, in epithelial cancer cell lines, in an effort to determine function. 10,11 microRNAs miR-451a and miR-144 have yet to be identified in any non-neoplastic cell type, yet they repeatedly are assigned non-RBC functionality due to tissue level data being confused for cell level expression data (Tables 1 and 2). 12-17 miR-486 is also abundant in platelets, but neither RBC nor platelet expression justifies its assigned role in a variety of disease states in which it is unlikely to participate. 18,19 Thus it is important to identify the cellular source of a tissue-level microRNA signature, which can be done by checking known datasets, 5,20 obtaining cell-specific data from the Sequence Read Archive or Gene Expression Omnibus, or measuring the microRNA by qPCR or northern blot in a cell type of interest.…”