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Nick Sampas

Showing results (1-10 of 9) with videos related to

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Science (New York, N.Y.)|October 30, 2010
Diversity of human copy number variation and multicopy genesPeter H Sudmant, Jacob O Kitzman, Francesca Antonacci, 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.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNAMichael T Barrett, Alicia Scheffer, Amir Ben-Dor, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Physiological Genomics|March 20, 2003
Identification of endothelial cell genes by combined database mining and microarray analysisMichael Ho, Eugene Yang, George Matcuk, et al.
American Journal of Human Genetics|February 29, 2008
The fine-scale and complex architecture of human copy-number variationGeorge H Perry, Amir Ben-Dor, Anya Tsalenko, 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.
Nature Genetics|December 25, 2007
Closing gaps in the human genome with fosmid resources generated from multiple individualsDonald Bovee, Yang Zhou, Eric Haugen, et al.
Nature|May 3, 2008
Mapping and sequencing of structural variation from eight human genomesJeffrey M Kidd, Gregory M Cooper, William F Donahue, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Science (New York, N.Y.)|October 30, 2010
Diversity of human copy number variation and multicopy genesPeter H Sudmant, Jacob O Kitzman, Francesca Antonacci, 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.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNAMichael T Barrett, Alicia Scheffer, Amir Ben-Dor, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Physiological Genomics|March 20, 2003
Identification of endothelial cell genes by combined database mining and microarray analysisMichael Ho, Eugene Yang, George Matcuk, et al.
American Journal of Human Genetics|February 29, 2008
The fine-scale and complex architecture of human copy-number variationGeorge H Perry, Amir Ben-Dor, Anya Tsalenko, 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.
Nature Genetics|December 25, 2007
Closing gaps in the human genome with fosmid resources generated from multiple individualsDonald Bovee, Yang Zhou, Eric Haugen, et al.
Nature|May 3, 2008
Mapping and sequencing of structural variation from eight human genomesJeffrey M Kidd, Gregory M Cooper, William F Donahue, et al.
Pageof 1