ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
cuteHap: Haplotype-Aware Structural Variant Detection in Phased Long-Read Sequencing Data.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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Who cites it
1 citing paper in PubMed.
- Protocol for haplotype-resolved structural variant detection via long-read sequencing using cuteHap.STAR protocols · 2026Article
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Authors and funding
8 authors.
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Abstract
Long-read sequencing has enabled comprehensive exploration of human genome at an unprecedented scale, particularly enhancing our understanding of structural variants (SVs). Phasing, a powerful approach for assigning haplotypes to sequencing reads, enables the generation of haplotype-aware call sets without requiring whole-genome assembly and provides a new direction for SV detection. Herein, we present cuteHap, a haplotype-aware SV detection method designed for phased long-read sequencing data. cuteHap fully leverages phased alignments and automatically selects a self-adaptive clustering strategy or a cluster credibility-prioritized beam search algorithm to achieve accurate haplotype-resolved SV calls. In addition, cuteHap incorporates a mosaic detection module to resolve somatic mosaicism. cuteHap achieved 6% and 3% higher F1-scores on Pacific Biosciences High-Fidelity (PacBio HiFi) and Oxford Nanopore Technologies (ONT) datasets, respectively, and detected a greater diversity of low-frequency SVs in tumor datasets. Its robust and high-performance SV detection facilitates the generation of high-quality haplotype-resolved call sets and advancing global genomic and genetic research.
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