Publications

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Author Title [ Year(Desc)]
Filters: Author is Carroll, Andrew  [Clear All Filters]
2019
Wenger, A. M. et al. Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nat Biotechnol 37, 1155-1162 (2019).
2020
Zarate, S. et al. Parliament2: Accurate structural variant calling at scale. Gigascience 9, (2020).
2021
Yun, T. et al. Accurate, scalable cohort variant calls using DeepVariant and GLnexus. Bioinformatics (2021). doi:10.1093/bioinformatics/btaa1081
Garg, S. et al. Chromosome-scale, haplotype-resolved assembly of human genomes. Nat Biotechnol 39, 309-312 (2021).