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Gigascience
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September 7, 2017
A recurrence-based approach for validating structural variation using long-read sequencing technology
Xuefang Zhao, Alexandra M Weber, Ryan E Mills
Nature Reviews. Genetics
|
November 16, 2019
Structural variation in the sequencing era
Steve S Ho, Alexander E Urban, Ryan E Mills
Gigascience
|
December 31, 2019
Prognostic model for multiple myeloma progression integrating gene expression and clinical features
Chen Sun, Hongyang Li, Ryan E Mills, et al.
Virus Evolution
|
October 25, 2016
CodonShuffle: a tool for generating and analyzing synonymously mutated sequences
Daniel Macedo de Melo Jorge, Ryan E Mills, Adam S Lauring
The Journal of Biological Chemistry
|
March 18, 2008
A PY-NLS nuclear targeting signal is required for nuclear localization and function of the Saccharomyces cerevisiae mRNA-binding protein Hrp1
Allison Lange, Ryan E Mills, Scott E Devine, et al.
Nucleic Acids Research
|
October 29, 2014
The genomic landscape of polymorphic human nuclear mitochondrial insertions
Gargi Dayama, Sarah B Emery, Jeffrey M Kidd, et al.
Human Molecular Genetics
|
September 23, 2010
Small insertions and deletions (INDELs) in human genomes
Julienne M Mullaney, Ryan E Mills, W Stephen Pittard, et al.
Trends in Genetics : TIG
|
March 3, 2007
Which transposable elements are active in the human genome?
Ryan E Mills, E Andrew Bennett, Rebecca C Iskow, et al.
BMC Bioinformatics
|
November 26, 2016
SPECtre: a spectral coherence--based classifier of actively translated transcripts from ribosome profiling sequence data
Sang Y Chun, Caitlin M Rodriguez, Peter K Todd, et al.
BMC Genomics
|
May 22, 2019
Translation of upstream open reading frames in a model of neuronal differentiation
Caitlin M Rodriguez, Sang Y Chun, Ryan E Mills, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Gigascience
|
September 7, 2017
A recurrence-based approach for validating structural variation using long-read sequencing technology
Xuefang Zhao, Alexandra M Weber, Ryan E Mills
Nature Reviews. Genetics
|
November 16, 2019
Structural variation in the sequencing era
Steve S Ho, Alexander E Urban, Ryan E Mills
Gigascience
|
December 31, 2019
Prognostic model for multiple myeloma progression integrating gene expression and clinical features
Chen Sun, Hongyang Li, Ryan E Mills, et al.
Virus Evolution
|
October 25, 2016
CodonShuffle: a tool for generating and analyzing synonymously mutated sequences
Daniel Macedo de Melo Jorge, Ryan E Mills, Adam S Lauring
The Journal of Biological Chemistry
|
March 18, 2008
A PY-NLS nuclear targeting signal is required for nuclear localization and function of the Saccharomyces cerevisiae mRNA-binding protein Hrp1
Allison Lange, Ryan E Mills, Scott E Devine, et al.
Nucleic Acids Research
|
October 29, 2014
The genomic landscape of polymorphic human nuclear mitochondrial insertions
Gargi Dayama, Sarah B Emery, Jeffrey M Kidd, et al.
Human Molecular Genetics
|
September 23, 2010
Small insertions and deletions (INDELs) in human genomes
Julienne M Mullaney, Ryan E Mills, W Stephen Pittard, et al.
Trends in Genetics : TIG
|
March 3, 2007
Which transposable elements are active in the human genome?
Ryan E Mills, E Andrew Bennett, Rebecca C Iskow, et al.
BMC Bioinformatics
|
November 26, 2016
SPECtre: a spectral coherence--based classifier of actively translated transcripts from ribosome profiling sequence data
Sang Y Chun, Caitlin M Rodriguez, Peter K Todd, et al.
BMC Genomics
|
May 22, 2019
Translation of upstream open reading frames in a model of neuronal differentiation
Caitlin M Rodriguez, Sang Y Chun, Ryan E Mills, et al.
Page
of 7