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Nature Methods
|
May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertions
Jeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Cell
|
May 8, 2012
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Nature Genetics
|
August 24, 2010
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
Francesca Antonacci, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Genome Research
|
October 23, 2020
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution
Flavia Angela Maria Maggiolini, Ashley D Sanders, Colin James Shew, et al.
Nature Genetics
|
October 20, 2014
Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability
Francesca Antonacci, Megan Y Dennis, John Huddleston, et al.
Nature Genetics
|
July 4, 2012
Structural diversity and African origin of the 17q21.31 inversion polymorphism
Karyn Meltz Steinberg, Francesca Antonacci, Peter H Sudmant, et al.
Science (New York, N.Y.)
|
October 19, 2019
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes
PingHsun Hsieh, Mitchell R Vollger, Vy Dang, et al.
Nature Genetics
|
January 24, 2009
Evolutionary toggling of the MAPT 17q21.31 inversion region
Michael C Zody, Zhaoshi Jiang, Hon-Chung Fung, et al.
Nature Ecology & Evolution
|
June 6, 2017
The evolution and population diversity of human-specific segmental duplications
Megan Y Dennis, Lana Harshman, Bradley J Nelson, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
Nature Methods
|
May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertions
Jeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Cell
|
May 8, 2012
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Nature Genetics
|
August 24, 2010
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
Francesca Antonacci, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Genome Research
|
October 23, 2020
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution
Flavia Angela Maria Maggiolini, Ashley D Sanders, Colin James Shew, et al.
Nature Genetics
|
October 20, 2014
Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability
Francesca Antonacci, Megan Y Dennis, John Huddleston, et al.
Nature Genetics
|
July 4, 2012
Structural diversity and African origin of the 17q21.31 inversion polymorphism
Karyn Meltz Steinberg, Francesca Antonacci, Peter H Sudmant, et al.
Science (New York, N.Y.)
|
October 19, 2019
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes
PingHsun Hsieh, Mitchell R Vollger, Vy Dang, et al.
Nature Genetics
|
January 24, 2009
Evolutionary toggling of the MAPT 17q21.31 inversion region
Michael C Zody, Zhaoshi Jiang, Hon-Chung Fung, et al.
Nature Ecology & Evolution
|
June 6, 2017
The evolution and population diversity of human-specific segmental duplications
Megan Y Dennis, Lana Harshman, Bradley J Nelson, et al.
Page
of 6