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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
|
July 10, 2023
Scalable, accessible, and reproducible reference genome assembly and evaluation in Galaxy
Delphine Larivière, Linelle Abueg, Nadolina Brajuka, 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.
Scientific Data
|
June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materials
Justin M Zook, David Catoe, Jennifer McDaniel, et al.
F1000Research
|
October 11, 2021
An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates
Ann M Mc Cartney, Medhat Mahmoud, Michael Jochum, et al.
Nature
|
April 29, 2021
Towards complete and error-free genome assemblies of all vertebrate species
Arang Rhie, Shane A McCarthy, Olivier Fedrigo, et al.
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 17 results.
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
|
July 10, 2023
Scalable, accessible, and reproducible reference genome assembly and evaluation in Galaxy
Delphine Larivière, Linelle Abueg, Nadolina Brajuka, 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.
Scientific Data
|
June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materials
Justin M Zook, David Catoe, Jennifer McDaniel, et al.
F1000Research
|
October 11, 2021
An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates
Ann M Mc Cartney, Medhat Mahmoud, Michael Jochum, et al.
Nature
|
April 29, 2021
Towards complete and error-free genome assemblies of all vertebrate species
Arang Rhie, Shane A McCarthy, Olivier Fedrigo, et al.
Page
of 2