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Nature Methods
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September 14, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail 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 methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, 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 methylation
Kimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Nature
|
April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversity
Ting Wang, Lucinda Antonacci-Fulton, Kerstin Howe, 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 inheritance
Monika 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 genomics
Nancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.
Science (New York, N.Y.)
|
March 31, 2022
Complete genomic and epigenetic maps of human centromeres
Nicolas Altemose, Glennis A Logsdon, Andrey V Bzikadze, et al.
Nature
|
October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomes
Erich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature
|
August 23, 2023
The complete sequence of a human Y chromosome
Arang Rhie, Sergey Nurk, Monika Cechova, et al.
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of 3
Search research articles
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Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Nature Methods
|
September 14, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail 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 methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, 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 methylation
Kimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Nature
|
April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversity
Ting Wang, Lucinda Antonacci-Fulton, Kerstin Howe, 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 inheritance
Monika 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 genomics
Nancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.
Science (New York, N.Y.)
|
March 31, 2022
Complete genomic and epigenetic maps of human centromeres
Nicolas Altemose, Glennis A Logsdon, Andrey V Bzikadze, et al.
Nature
|
October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomes
Erich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature
|
August 23, 2023
The complete sequence of a human Y chromosome
Arang Rhie, Sergey Nurk, Monika Cechova, et al.
Page
of 3