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Gigascience|December 12, 2025
Challenges in structural variant calling in low-complexity regionsQian Qin, Heng Li
Biorxiv : the Preprint Server for Biology|November 24, 2025
Improving long-read somatic structural variant calling with pangenome and de novo personal genome assemblyQian Qin, Jakob Heinz, Heng Li
Genomics, Proteomics & Bioinformatics|September 19, 2025
colorSV: Long-range Somatic Structural Variation Calling from Matched Tumor-normal Co-assembly GraphsMegan K Le, Qian Qin, Heng Li
Biorxiv : the Preprint Server for Biology|November 24, 2025
FuFiHLA: A tool for Full-Field HLA typing from long reads dataJingqing Hu, Qian Qin, Heng Li, et al.
Bioinformatics (Oxford, England)|May 5, 2026
FuFiHLA: A tool for Full-Field HLA typing from long-read dataJingqing Hu, Qian Qin, Heng Li, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Diploid donor-specific assembly enhances somatic structural variant detection in cancer genomesYuwei Zhang, Han Qu, Qian Qin, et al.
Bioinformatics (Oxford, England)|January 17, 2023
Protein-to-genome alignment with miniprotHeng Li
Bioinformatics (Oxford, England)|February 16, 2011
Improving SNP discovery by base alignment qualityHeng Li
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