Evidence map›Paper›PMID 41677369›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

cuteHap: Haplotype-Aware Structural Variant Detection in Phased Long-Read Sequencing Data.

Shuqi Cao, Yadong Liu, Miao Cui, Runtian Gao, Weimin Guo, Guohua Wang, Yadong Wang, Tao Jiang

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Shuqi CaoCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.ORCID https://orcid.org/0000-0002-1163-2797
Yadong LiuCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Miao CuiCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Runtian GaoCollege of Life Sciences, Northeast Forestry University, Harbin, Heilongjiang, China.
Weimin GuoCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Guohua WangCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Yadong WangCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Tao JiangCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, China.ORCID https://orcid.org/0000-0002-0673-8503

Funding

Key Research and Development Program of Heilongjiang Province 2022ZX02C20National Key Research and Development Program of China 2024YFC3406303National Natural Science Foundation of China 62331012National Natural Science Foundation of China 62472120
6 · The paper itself

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.

Indexed as

Genome, HumanGenomic Structural VariationHaplotypesHigh-Throughput Nucleotide SequencingSequence Analysis, DNAAlgorithmsHumansSoftwaregenomic analysishaplotype‐awarelong‐read sequencingphasingsomatic mosaicismstructural variationsvariant calling

Identifiers

PMID41677369
PMCPMC13088286

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.