Refreshing results…
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Download from www.nature.comPangenomics enables genotyping of known structural variants in 5202 diverse genomes
UploadA population-specific reference panel for improved genotype imputation in African Americans
Download from www.nature.comAccurate, scalable cohort variant calls using DeepVariant and GLnexus
UploadMissing publications? Search for publications with a matching author name.