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Nature Methods|September 14, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylationMikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.Biorxiv : the Preprint Server for Biology|January 30, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylationMikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.Biorxiv : the Preprint Server for Biology|April 3, 2026
A Complete Genome for the Common MarmosetPrajna Hebbar, Tamara Potapova, Hailey Loucks, et al.Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.Biorxiv : the Preprint Server for Biology|December 31, 2025
Complete genomes of a multi-generational pedigree to expand studies of genetic and epigenetic inheritanceMonika Cechova, Tamara A Potapova, Andreas Rechtsteiner, et al.Biorxiv : the Preprint Server for Biology|September 26, 2025
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.Pageof 2