Refreshing results…
Curated variation benchmarks for challenging medically relevant autosomal genes
Download from www.nature.comPerformance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study
Download from www.nature.comSomatic variant analysis of linked-reads sequencing data with Lancet
Download from academic.oup.comBenchmarking challenging small variants with linked and long reads
Download from doi.orgA crowdsourced set of curated structural variants for the human genome
Download from doi.orgA strategy for building and using a human reference pangenome
Download from doi.orgGenome-wide somatic variant calling using localized colored de Bruijn graphs
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