This poster from Q2 Solutions describes a study across two organizations using matched donor cryopreserved human peripheral blood mononuclear cells and bone marrow mononuclear cells to examine the performance and reproducibility of CITE-Seq on the 10x Genomics Chromium platform.
Emerging single-cell multiomic techniques like CITE-Seq require best practices, optimized parameters, and an understanding of practical limitations when comparing data from different labs, especially when analyzing clinically relevant samples.
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