Genome biology · 2025 · 18 citations · 42 references
Life SciencesBioinformaticsGeneticsGenomic Data AnalysisGenomic InformaticsGenomicsComputational GenomicsDna SequencingNext-generation SequencingStructural Variant AnalysisVariant CallingVariant DetectionApplication EfficiencyClusteringDe Novo Structural Variant DiscoveryStructural Variant BenchmarkingStructural Variant DetectionVariant BenchmarkingVariant Calling BenchmarkingVariant Calling From Long Reads
Long-read sequencing technologies have great potential for the comprehensive discovery of structural variations (SVs). However, accurate genotype assignment for SVs remains challenging due to unavoidable sequencing errors, limited coverage, and the complexity of SVs. Herein, we propose cuteFC, which employs self-adaptive clustering along with a multiallele-aware clustering to achieve accurate SV regenotyping through a force-calling approach. cuteFC also applies a Genome Position Scanner algorithm to improve its application efficiency. Benchmarking evaluations demonstrate that cuteFC outperforms state-of-the-art methods with 2-5% higher F1 scores and constructs a higher-quality genomic atlas with minimal computational resources. cuteFC is available at https://github.com/Meltpinkg/cuteFC and https://zenodo.org/records/14671406 .
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Twelve years of SAMtools and BCFtools
Petr Danecek, James Bonfield, Jennifer Liddle et al. · GigaScience · 2021 · 15.9K citations · Full text
Haplotype-resolved de novo assembly using phased assembly graphs with hifiasm
Nature Methods · 2021 · 5.5K citations · Full text
An integrated map of structural variation in 2,504 human genomes
Peter H. Sudmant, Tobias Rausch, Eugene J. Gardner et al. · Nature · 2015 · 2.7K citations · Full text