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Methods in Molecular Biology (Clifton, N.J.)
|
March 24, 2016
Variant Calling From Next Generation Sequence Data
Nancy F Hansen
BMC Bioinformatics
|
July 30, 2015
Evaluation of variant detection software for pooled next-generation sequence data
Howard W Huang, , James C Mullikin, et al.
G3 (Bethesda, Md.)
|
July 12, 2018
The Sleep Inbred Panel, a Collection of Inbred <i>Drosophila melanogaster</i> with Extreme Long and Short Sleep Duration
Yazmin L Serrano Negron, Nancy F Hansen, Susan T Harbison
Nature Methods
|
April 2, 2022
Long-read mapping to repetitive reference sequences using Winnowmap2
Chirag Jain, Arang Rhie, Nancy F Hansen, et al.
Plos Genetics
|
December 15, 2017
Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep
Susan T Harbison, Yazmin L Serrano Negron, Nancy F Hansen, et al.
Plos One
|
April 22, 2020
Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans
Zhi Liu, Daniel Shriner, Nancy F Hansen, et al.
Bioinformatics (Oxford, England)
|
April 27, 2013
Shimmer: detection of genetic alterations in tumors using next-generation sequence data
Nancy F Hansen, Jared J Gartner, Lan Mei, et al.
F1000Research
|
January 10, 2019
NovoGraph: Human genome graph construction from multiple long-read <i>de novo</i> assemblies
Evan Biederstedt, Jeffrey C Oliver, Nancy F Hansen, et al.
American Journal of Human Genetics
|
May 11, 2010
Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate
Jennifer J Johnston, Jamie K Teer, Praveen F Cherukuri, et al.
Developmental Biology
|
April 28, 2015
The transcription factors Ets1 and Sox10 interact during murine melanocyte development
Amy Saldana-Caboverde, Erasmo M Perera, Dawn E Watkins-Chow, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 6
Methods in Molecular Biology (Clifton, N.J.)
|
March 24, 2016
Variant Calling From Next Generation Sequence Data
Nancy F Hansen
BMC Bioinformatics
|
July 30, 2015
Evaluation of variant detection software for pooled next-generation sequence data
Howard W Huang, , James C Mullikin, et al.
G3 (Bethesda, Md.)
|
July 12, 2018
The Sleep Inbred Panel, a Collection of Inbred <i>Drosophila melanogaster</i> with Extreme Long and Short Sleep Duration
Yazmin L Serrano Negron, Nancy F Hansen, Susan T Harbison
Nature Methods
|
April 2, 2022
Long-read mapping to repetitive reference sequences using Winnowmap2
Chirag Jain, Arang Rhie, Nancy F Hansen, et al.
Plos Genetics
|
December 15, 2017
Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep
Susan T Harbison, Yazmin L Serrano Negron, Nancy F Hansen, et al.
Plos One
|
April 22, 2020
Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans
Zhi Liu, Daniel Shriner, Nancy F Hansen, et al.
Bioinformatics (Oxford, England)
|
April 27, 2013
Shimmer: detection of genetic alterations in tumors using next-generation sequence data
Nancy F Hansen, Jared J Gartner, Lan Mei, et al.
F1000Research
|
January 10, 2019
NovoGraph: Human genome graph construction from multiple long-read <i>de novo</i> assemblies
Evan Biederstedt, Jeffrey C Oliver, Nancy F Hansen, et al.
American Journal of Human Genetics
|
May 11, 2010
Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate
Jennifer J Johnston, Jamie K Teer, Praveen F Cherukuri, et al.
Developmental Biology
|
April 28, 2015
The transcription factors Ets1 and Sox10 interact during murine melanocyte development
Amy Saldana-Caboverde, Erasmo M Perera, Dawn E Watkins-Chow, et al.
Page
of 6