Supplementary data for "Benchmarking short-read germline structural variant calling for research and clinic highlights advantages of using ensembles of tools and small impact of graph genome alignment"
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Per-sample (eg NA12878) and per alignment (eg graph vs linear) folders containing:- VCF output (both pre-processing (eg linear-Smoove-NA12878.vcf.gz) and post-processing (linear-Smoove-NA12878.final.vcf.gz))- Truvari type-ignore standard output (fp.vcf.gz, fn, tp-comp, tp-base, summary.json)Bam used for NA12878 graph:2188.v4.2.4.grc38_HPRCv1X.bam
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Zenodo创建时间：
2026-06-09
