Benchmarking short-read germline structural variant calling highlights advantages of using ensembles of tools and small impact of graph genome alignment.
Journal: Genome biology
•
Abstract
Abstract text is not embedded in this discovery record. Please consult the full-text publication via the source link on the right.
Subjects & Keywords
How to Cite this Article
Guo Y, Sofie Engdal E, Kodama M, et al. (2026). "Benchmarking short-read germline structural variant calling highlights advantages of using ensembles of tools and small impact of graph genome alignment.". Genome biology. https://doi.org/10.1186/s13059-026-04219-3