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Targeted Genomic Sequencing in Large Human Genes to Detect Induced Structural Variants

svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing

T. E. Wilson, Samreen Ahmed, J. Higgins, et al. (2022). NAR Genomics and Bioinformatics. Cited 4 times. https://doi.org/10.1093/nargab/lqad042