ArticleSTAR protocols2026
LOTR-Seq: A protocol for large-scale simultaneous single-cell long-read genotyping of transcripts.
Article in STAR protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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9 authors.
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Abstract
Single-cell RNA sequencing enables analysis of intra-tumoral transcriptional heterogeneity but has limited coverage of mutational hotspots. Here, we present LOTR-Seq, a protocol combining short-read whole-transcriptome analysis with long-read genotyping. We describe steps for hematopoietic stem cell isolation from human bone marrow samples, generation of full-length single-cell barcoded cDNA, target enrichment, and long-read sequencing for variant calling. For complete details on the use and execution of this protocol, please refer to Grabek et al.
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