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Eric S Lander

Showing results (101-110 of 347) with videos related to

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Nature|January 7, 2014
Discovery and saturation analysis of cancer genes across 21 tumour typesMichael S Lawrence, Petar Stojanov, Craig H Mermel, et al.
Nature Methods|December 17, 2008
Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencingChad Nusbaum, Toshiro K Ohsumi, James Gomez, et al.
European Journal of Human Genetics : EJHG|April 13, 2017
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panelMario Mitt, Mart Kals, Kalle Pärn, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2002
Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cellsChang-Zheng Chen, Min Li, David de Graaf, et al.
Cell Stem Cell|June 24, 2010
Wilms tumor chromatin profiles highlight stem cell properties and a renal developmental networkAviva Presser Aiden, Miguel N Rivera, Esther Rheinbay, et al.
Genomics|March 28, 2003
Pathogen discovery from human tissue by sequence-based computational subtractionYaohui Xu, Nicole Stange-Thomann, Griffin Weber, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2017
Systematic dissection of genomic features determining transcription factor binding and enhancer functionSharon R Grossman, Xiaolan Zhang, Li Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2005
An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencingElliott H Margulies, Jade P Vinson, , et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2005
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profilesAravind Subramanian, Pablo Tamayo, Vamsi K Mootha, et al.
Nature Genetics|August 15, 2018
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutationsAmit V Khera, Mark Chaffin, Krishna G Aragam, et al.
Pageof 35

Showing results (101-110 of 347) with videos related to

Sort By:
Pageof 35
Nature|January 7, 2014
Discovery and saturation analysis of cancer genes across 21 tumour typesMichael S Lawrence, Petar Stojanov, Craig H Mermel, et al.
Nature Methods|December 17, 2008
Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencingChad Nusbaum, Toshiro K Ohsumi, James Gomez, et al.
European Journal of Human Genetics : EJHG|April 13, 2017
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panelMario Mitt, Mart Kals, Kalle Pärn, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2002
Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cellsChang-Zheng Chen, Min Li, David de Graaf, et al.
Cell Stem Cell|June 24, 2010
Wilms tumor chromatin profiles highlight stem cell properties and a renal developmental networkAviva Presser Aiden, Miguel N Rivera, Esther Rheinbay, et al.
Genomics|March 28, 2003
Pathogen discovery from human tissue by sequence-based computational subtractionYaohui Xu, Nicole Stange-Thomann, Griffin Weber, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2017
Systematic dissection of genomic features determining transcription factor binding and enhancer functionSharon R Grossman, Xiaolan Zhang, Li Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2005
An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencingElliott H Margulies, Jade P Vinson, , et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2005
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profilesAravind Subramanian, Pablo Tamayo, Vamsi K Mootha, et al.
Nature Genetics|August 15, 2018
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutationsAmit V Khera, Mark Chaffin, Krishna G Aragam, et al.
Pageof 35