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Ninety percent of drug candidates fail to reach the commercial market—and among those failures, 90% are linked to suboptimal target selection. With a product’s odds of success so closely tied to good target characterization, scientists are always looking for the best way to create a supportive foundation for their asset during drug discovery.
Single-cell RNA sequencing (scRNA-seq) is a proven practice that does exactly that—but its uptake by biopharma organizations has been limited. A retrospective analysis that examines scRNA-seq data across multiple diseases and tissue types may change this approach. In this webinar, the study’s co-author discusses:
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