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W Scott Watkins

Showing results (21-30 of 57) with videos related to

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Annals of Human Genetics|March 6, 2010
Limited distribution of a cardiomyopathy-associated variant in IndiaTatum S Simonson, Yuhua Zhang, Chad D Huff, et al.
Nucleic Acids Research|February 19, 2020
TypeTE: a tool to genotype mobile element insertions from whole genome resequencing dataClément Goubert, Jainy Thomas, Lindsay M Payer, et al.
Molecular Biology and Evolution|June 5, 2003
Following the LINEs: an analysis of primate genomic variation at human-specific LINE-1 insertion sitesBethaney J Vincent, Jeremy S Myers, Huei Jin Ho, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2015
Two contemporaneous mitogenomes from terminal Pleistocene burials in eastern BeringiaJustin C Tackney, Ben A Potter, Jennifer Raff, et al.
Cancer Genetics|July 4, 2012
EWS/FLI-responsive GGAA microsatellites exhibit polymorphic differences between European and African populationsRobert Beck, Michael J Monument, W Scott Watkins, et al.
BMC Genomics|May 24, 2017
Extremely low-coverage whole genome sequencing in South Asians captures population genomics informationNavin Rustagi, Anbo Zhou, W Scott Watkins, et al.
Plos Genetics|July 23, 2013
Genomic analysis of natural selection and phenotypic variation in high-altitude mongoliansJinchuan Xing, Tana Wuren, Tatum S Simonson, et al.
Genome Research|May 5, 2009
Fine-scaled human genetic structure revealed by SNP microarraysJinchuan Xing, W Scott Watkins, David J Witherspoon, et al.
Human Genomics|December 14, 2004
Genome-wide analysis of the human Alu Yb-lineageAnthony B Carter, Abdel-Halim Salem, Dale J Hedges, et al.
G3 (Bethesda, Md.)|September 1, 2018
Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing HeritabilityJiun-Sheng Chen, Fulan Hu, Subra Kugathasan, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Annals of Human Genetics|March 6, 2010
Limited distribution of a cardiomyopathy-associated variant in IndiaTatum S Simonson, Yuhua Zhang, Chad D Huff, et al.
Nucleic Acids Research|February 19, 2020
TypeTE: a tool to genotype mobile element insertions from whole genome resequencing dataClément Goubert, Jainy Thomas, Lindsay M Payer, et al.
Molecular Biology and Evolution|June 5, 2003
Following the LINEs: an analysis of primate genomic variation at human-specific LINE-1 insertion sitesBethaney J Vincent, Jeremy S Myers, Huei Jin Ho, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2015
Two contemporaneous mitogenomes from terminal Pleistocene burials in eastern BeringiaJustin C Tackney, Ben A Potter, Jennifer Raff, et al.
Cancer Genetics|July 4, 2012
EWS/FLI-responsive GGAA microsatellites exhibit polymorphic differences between European and African populationsRobert Beck, Michael J Monument, W Scott Watkins, et al.
BMC Genomics|May 24, 2017
Extremely low-coverage whole genome sequencing in South Asians captures population genomics informationNavin Rustagi, Anbo Zhou, W Scott Watkins, et al.
Plos Genetics|July 23, 2013
Genomic analysis of natural selection and phenotypic variation in high-altitude mongoliansJinchuan Xing, Tana Wuren, Tatum S Simonson, et al.
Genome Research|May 5, 2009
Fine-scaled human genetic structure revealed by SNP microarraysJinchuan Xing, W Scott Watkins, David J Witherspoon, et al.
Human Genomics|December 14, 2004
Genome-wide analysis of the human Alu Yb-lineageAnthony B Carter, Abdel-Halim Salem, Dale J Hedges, et al.
G3 (Bethesda, Md.)|September 1, 2018
Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing HeritabilityJiun-Sheng Chen, Fulan Hu, Subra Kugathasan, et al.
Pageof 6