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Bioinformatics (Oxford, England)
|
April 1, 2021
ASHLEYS: automated quality control for single-cell Strand-seq data
Christina Gros, Ashley D Sanders, Jan O Korbel, et al.
Genome Research
|
July 31, 2016
Characterizing polymorphic inversions in human genomes by single-cell sequencing
Ashley D Sanders, Mark Hills, David Porubský, et al.
Nature Protocols
|
May 12, 2017
Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs
Ashley D Sanders, Ester Falconer, Mark Hills, et al.
Bioinformatics (Oxford, England)
|
September 11, 2019
breakpointR: an R/Bioconductor package to localize strand state changes in Strand-seq data
David Porubsky, Ashley D Sanders, Aaron Taudt, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Construction of Whole Genomes from Scaffolds Using Single Cell Strand-Seq Data
Mark Hills, Ester Falconer, Kieran O'Neill, et al.
Nature Communications
|
November 5, 2017
Dense and accurate whole-chromosome haplotyping of individual genomes
David Porubsky, Shilpa Garg, Ashley D Sanders, et al.
Bioinformatics (Oxford, England)
|
June 29, 2018
Strand-seq enables reliable separation of long reads by chromosome via expectation maximization
Maryam Ghareghani, David Porubskỳ, Ashley D Sanders, et al.
Nature Methods
|
October 9, 2012
DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution
Ester Falconer, Mark Hills, Ulrike Naumann, et al.
Genome Research
|
September 21, 2016
Direct chromosome-length haplotyping by single-cell sequencing
David Porubský, Ashley D Sanders, Niek van Wietmarschen, et al.
Plos One
|
September 21, 2011
Adult spinal cord radial glia display a unique progenitor phenotype
Audrey Petit, Ashley D Sanders, Timothy E Kennedy, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Bioinformatics (Oxford, England)
|
April 1, 2021
ASHLEYS: automated quality control for single-cell Strand-seq data
Christina Gros, Ashley D Sanders, Jan O Korbel, et al.
Genome Research
|
July 31, 2016
Characterizing polymorphic inversions in human genomes by single-cell sequencing
Ashley D Sanders, Mark Hills, David Porubský, et al.
Nature Protocols
|
May 12, 2017
Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs
Ashley D Sanders, Ester Falconer, Mark Hills, et al.
Bioinformatics (Oxford, England)
|
September 11, 2019
breakpointR: an R/Bioconductor package to localize strand state changes in Strand-seq data
David Porubsky, Ashley D Sanders, Aaron Taudt, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Construction of Whole Genomes from Scaffolds Using Single Cell Strand-Seq Data
Mark Hills, Ester Falconer, Kieran O'Neill, et al.
Nature Communications
|
November 5, 2017
Dense and accurate whole-chromosome haplotyping of individual genomes
David Porubsky, Shilpa Garg, Ashley D Sanders, et al.
Bioinformatics (Oxford, England)
|
June 29, 2018
Strand-seq enables reliable separation of long reads by chromosome via expectation maximization
Maryam Ghareghani, David Porubskỳ, Ashley D Sanders, et al.
Nature Methods
|
October 9, 2012
DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution
Ester Falconer, Mark Hills, Ulrike Naumann, et al.
Genome Research
|
September 21, 2016
Direct chromosome-length haplotyping by single-cell sequencing
David Porubský, Ashley D Sanders, Niek van Wietmarschen, et al.
Plos One
|
September 21, 2011
Adult spinal cord radial glia display a unique progenitor phenotype
Audrey Petit, Ashley D Sanders, Timothy E Kennedy, et al.
Page
of 4