Lv1
10 积分 2025-07-25 加入
Accurate detection of complex structural variations using single-molecule sequencing
2个月前
已完结
A synthetic-diploid benchmark for accurate variant-calling evaluation
2个月前
已完结
Enhanced detection and genotyping of disease-associated tandem repeats using HMMSTR and targeted long-read sequencing
5个月前
已关闭
Improving long-read somatic structural variant calling with pangenome and de novo personal genome assembly
5个月前
已完结
Picky comprehensively detects high-resolution structural variants in nanopore long reads (Nature Methods)
5个月前
已完结
Multi-platform discovery of haplotype-resolved structural variation in human genomes
6个月前
已完结
SVision: a deep learning approach to resolve complex structural variants
6个月前
已完结
A graph neural network approach for accurate prediction of pathogenicity in multi-type variants
6个月前
已完结
Graph neural networks for single-cell omics data: a review of approaches and applications
6个月前
已完结
Graph Neural Networks and Their Current Applications in Bioinformatics
6个月前
已完结
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