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Maika Malig

Showing results (11-20 of 40) with videos related to

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Cell|November 30, 2010
A human genome structural variation sequencing resource reveals insights into mutational mechanismsJeffrey M Kidd, Tina Graves, Tera L Newman, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 2015
Bovine NK-lysin: Copy number variation and functional diversificationJunfeng Chen, John Huddleston, Reuben M Buckley, et al.
Genes and Immunity|October 24, 2014
Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityCorey T Watson, Karyn Meltz Steinberg, Tina A Graves, et al.
American Journal of Human Genetics|March 15, 2011
Population-genetic properties of differentiated human copy-number polymorphismsCatarina D Campbell, Nick Sampas, Anya Tsalenko, et al.
Scientific Reports|February 4, 2017
Epigenetic origin of evolutionary novel centromeresDoron Tolomeo, Oronzo Capozzi, Roscoe R Stanyon, et al.
Haematologica|January 15, 2026
Evaluation of acute myeloid leukemia using genomic proximity mapping-based next generation cytogenomicsCecilia C S Yeung, Stephen M Eacker, Olga Sala-Torra, et al.
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.
Nature Genetics|September 25, 2012
Estimating the human mutation rate using autozygosity in a founder populationCatarina D Campbell, Jessica X Chong, Maika Malig, 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.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Cell|November 30, 2010
A human genome structural variation sequencing resource reveals insights into mutational mechanismsJeffrey M Kidd, Tina Graves, Tera L Newman, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 2015
Bovine NK-lysin: Copy number variation and functional diversificationJunfeng Chen, John Huddleston, Reuben M Buckley, et al.
Genes and Immunity|October 24, 2014
Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityCorey T Watson, Karyn Meltz Steinberg, Tina A Graves, et al.
American Journal of Human Genetics|March 15, 2011
Population-genetic properties of differentiated human copy-number polymorphismsCatarina D Campbell, Nick Sampas, Anya Tsalenko, et al.
Scientific Reports|February 4, 2017
Epigenetic origin of evolutionary novel centromeresDoron Tolomeo, Oronzo Capozzi, Roscoe R Stanyon, et al.
Haematologica|January 15, 2026
Evaluation of acute myeloid leukemia using genomic proximity mapping-based next generation cytogenomicsCecilia C S Yeung, Stephen M Eacker, Olga Sala-Torra, et al.
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.
Nature Genetics|September 25, 2012
Estimating the human mutation rate using autozygosity in a founder populationCatarina D Campbell, Jessica X Chong, Maika Malig, 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.
Pageof 4