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starlabs To limit the number of false-positive doublets, which are common in snRNA-seq demultiplexing owing to background RNA and potential large duplications or deletions shared by tumours in the same cohort, we used the gnomADv4 exome data to subset only the most likely germline variants https://lookaside.instagram.com/seo/google_widget/crawler/?media_id=3862815505783121926 Scent:Plumeria MIC+B12 Injectable — Prescription | Vivo

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