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Can Alkan

Showing results (71-80 of 104) with videos related to

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Nature Genetics|September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencingCan 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 disorderSanthosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Genome Research|January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technologyJohn Huddleston, Swati Ranade, Maika Malig, et al.
Genome Biology|August 27, 2021
Technology dictates algorithms: recent developments in read alignmentMohammed Alser, Jeremy Rotman, Dhrithi Deshpande, et al.
Genome Research|February 4, 2012
Copy number variation of individual cattle genomes using next-generation sequencingDerek M Bickhart, Yali Hou, Steven G Schroeder, et al.
Nature|August 20, 2004
The structure and evolution of centromeric transition regions within the human genomeXinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
Nature Methods|May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertionsJeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Genome Research|June 21, 2011
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzeeMario Ventura, Claudia R Catacchio, Can Alkan, et al.
Nature Communications|May 5, 2026
Rapid adaptive increase of amylase gene copy number in Indigenous AndeansKendra 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 riskFrancesca Antonacci, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Nature Genetics|September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencingCan 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 disorderSanthosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Genome Research|January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technologyJohn Huddleston, Swati Ranade, Maika Malig, et al.
Genome Biology|August 27, 2021
Technology dictates algorithms: recent developments in read alignmentMohammed Alser, Jeremy Rotman, Dhrithi Deshpande, et al.
Genome Research|February 4, 2012
Copy number variation of individual cattle genomes using next-generation sequencingDerek M Bickhart, Yali Hou, Steven G Schroeder, et al.
Nature|August 20, 2004
The structure and evolution of centromeric transition regions within the human genomeXinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
Nature Methods|May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertionsJeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Genome Research|June 21, 2011
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzeeMario Ventura, Claudia R Catacchio, Can Alkan, et al.
Nature Communications|May 5, 2026
Rapid adaptive increase of amylase gene copy number in Indigenous AndeansKendra 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 riskFrancesca Antonacci, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Pageof 11