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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.
Science (New York, N.Y.)|March 31, 2022
From telomere to telomere: The transcriptional and epigenetic state of human repeat elementsSavannah J Hoyt, Jessica M Storer, Gabrielle A Hartley, et al.
Genes and Immunity|October 29, 2020
Multi-ancestry fine mapping of interferon lambda and the outcome of acute hepatitis C virus infectionCandelaria Vergara, Priya Duggal, Chloe L Thio, 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.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Population-scale Long-read Sequencing in the All of Us Research ProgramKiran V Garimella, Qiuhui Li, Julie Wertz, et al.
Nature|July 15, 2020
Telomere-to-telomere assembly of a complete human X chromosomeKaren H Miga, Sergey Koren, Arang Rhie, et al.
Science (New York, N.Y.)|March 31, 2022
Complete genomic and epigenetic maps of human centromeresNicolas Altemose, Glennis A Logsdon, Andrey V Bzikadze, 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.
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