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ANCHOR: haplotype-aware allelic and isoform inference from single-cell long-read RNA sequencing with de novo variant calling

2026-06-11

Abstract excerpt

Long-read RNA sequencing enables haplotype– and isoform-resolved allelic analysis of transcriptomes, yet extending this capability to single cells and distinct cell types remains computationally challenging due to sparse coverage, sequencing errors, incomplete variant information, and reference-biased transcript assignment. Here we present ANCHOR, a haplotype-aware framework for single-cell long-read RNA sequencin...

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Literature Corpus work
cd81538d-8c06-575e-97dc-f5c1937c85a3
DOI
10.64898/2026.06.08.730656
Open publication

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ANCHOR: haplotype-aware allelic and isoform inference from single-cell long-read RNA sequencing with de novo variant callingDOI 10.64898/2026.06.08.730656
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