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Lars Feuk

Showing results (91-100 of 103) with videos related to

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Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Gigascience|November 2, 2017
A 3-way hybrid approach to generate a new high-quality chimpanzee reference genome (Pan_tro_3.0)Lukas F K Kuderna, Chad Tomlinson, LaDeana W Hillier, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Nature Genetics|March 10, 2009
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaPaul A Northcott, Yukiko Nakahara, Xiaochong Wu, et al.
American Journal of Human Genetics|February 7, 2008
Structural variation of chromosomes in autism spectrum disorderChristian R Marshall, Abdul Noor, John B Vincent, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 10, 2025
Nationwide multicentre study of Nanopore long-read sequencing for 16S rRNA-species identificationSofia Brunet, Anna Grankvist, Daniel Jaen-Luchoro, et al.
Plos Biology|September 7, 2007
The diploid genome sequence of an individual humanSamuel Levy, Granger Sutton, Pauline C Ng, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Gigascience|November 2, 2017
A 3-way hybrid approach to generate a new high-quality chimpanzee reference genome (Pan_tro_3.0)Lukas F K Kuderna, Chad Tomlinson, LaDeana W Hillier, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Nature Genetics|March 10, 2009
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaPaul A Northcott, Yukiko Nakahara, Xiaochong Wu, et al.
American Journal of Human Genetics|February 7, 2008
Structural variation of chromosomes in autism spectrum disorderChristian R Marshall, Abdul Noor, John B Vincent, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 10, 2025
Nationwide multicentre study of Nanopore long-read sequencing for 16S rRNA-species identificationSofia Brunet, Anna Grankvist, Daniel Jaen-Luchoro, et al.
Plos Biology|September 7, 2007
The diploid genome sequence of an individual humanSamuel Levy, Granger Sutton, Pauline C Ng, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Pageof 11