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Nature
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January 7, 2014
Discovery and saturation analysis of cancer genes across 21 tumour types
Michael S Lawrence, Petar Stojanov, Craig H Mermel, et al.
Nature Methods
|
December 17, 2008
Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing
Chad 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 panel
Mario 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 cells
Chang-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 network
Aviva Presser Aiden, Miguel N Rivera, Esther Rheinbay, et al.
Genomics
|
March 28, 2003
Pathogen discovery from human tissue by sequence-based computational subtraction
Yaohui 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 function
Sharon 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 sequencing
Elliott 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 profiles
Aravind 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 mutations
Amit V Khera, Mark Chaffin, Krishna G Aragam, et al.
Page
of 35
Search research articles
Search
Showing results (101-110 of 347) with videos related to
Sort By:
Page
of 35
Nature
|
January 7, 2014
Discovery and saturation analysis of cancer genes across 21 tumour types
Michael S Lawrence, Petar Stojanov, Craig H Mermel, et al.
Nature Methods
|
December 17, 2008
Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing
Chad 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 panel
Mario 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 cells
Chang-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 network
Aviva Presser Aiden, Miguel N Rivera, Esther Rheinbay, et al.
Genomics
|
March 28, 2003
Pathogen discovery from human tissue by sequence-based computational subtraction
Yaohui 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 function
Sharon 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 sequencing
Elliott 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 profiles
Aravind 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 mutations
Amit V Khera, Mark Chaffin, Krishna G Aragam, et al.
Page
of 35