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Towards Generalist Biomedical AI
UploadAccelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Download from www.nature.comUltrarapid Nanopore Genome Sequencing in a Critical Care Setting
UploadPangenomics enables genotyping of known structural variants in 5202 diverse genomes
UploadAccurate, scalable cohort variant calls using DeepVariant and GLnexus
UploadA crowdsourced set of curated structural variants for the human genome
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