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Nature Genetics
|
September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencing
Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
American Journal of Human Genetics
|
February 5, 2013
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
Santhosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Genome Research
|
January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technology
John Huddleston, Swati Ranade, Maika Malig, et al.
Genome Biology
|
August 27, 2021
Technology dictates algorithms: recent developments in read alignment
Mohammed Alser, Jeremy Rotman, Dhrithi Deshpande, et al.
Genome Research
|
February 4, 2012
Copy number variation of individual cattle genomes using next-generation sequencing
Derek M Bickhart, Yali Hou, Steven G Schroeder, et al.
Nature
|
August 20, 2004
The structure and evolution of centromeric transition regions within the human genome
Xinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
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.
Genome Research
|
June 21, 2011
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee
Mario Ventura, Claudia R Catacchio, Can Alkan, et al.
Nature Communications
|
May 5, 2026
Rapid adaptive increase of amylase gene copy number in Indigenous Andeans
Kendra Scheer, Luane J B Landau, Kelsey Jorgensen, 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.
Page
of 11
Search research articles
Search
Showing results (71-80 of 104) with videos related to
Sort By:
Page
of 11
Nature Genetics
|
September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencing
Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
American Journal of Human Genetics
|
February 5, 2013
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
Santhosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Genome Research
|
January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technology
John Huddleston, Swati Ranade, Maika Malig, et al.
Genome Biology
|
August 27, 2021
Technology dictates algorithms: recent developments in read alignment
Mohammed Alser, Jeremy Rotman, Dhrithi Deshpande, et al.
Genome Research
|
February 4, 2012
Copy number variation of individual cattle genomes using next-generation sequencing
Derek M Bickhart, Yali Hou, Steven G Schroeder, et al.
Nature
|
August 20, 2004
The structure and evolution of centromeric transition regions within the human genome
Xinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
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.
Genome Research
|
June 21, 2011
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee
Mario Ventura, Claudia R Catacchio, Can Alkan, et al.
Nature Communications
|
May 5, 2026
Rapid adaptive increase of amylase gene copy number in Indigenous Andeans
Kendra Scheer, Luane J B Landau, Kelsey Jorgensen, 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.
Page
of 11