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Lukas Habegger

Showing results (11-20 of 41) with videos related to

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Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2010
Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencingJia Qian Wu, Lukas Habegger, Parinya Noisa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variantsBrenda Finucane, Matthew T Oetjens, Alicia Johns, et al.
Genome Biology|September 7, 2012
The GENCODE pseudogene resourceBaikang Pei, Cristina Sisu, Adam Frankish, et al.
Genome Biology|October 23, 2010
FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing dataAndrea Sboner, Lukas Habegger, Dorothee Pflueger, et al.
JAMA Psychiatry|July 23, 2020
Identification of Neuropsychiatric Copy Number Variants in a Health Care System PopulationChrista Lese Martin, Karen E Wain, Matthew T Oetjens, et al.
Nature Biotechnology|December 20, 2011
Performance comparison of whole-genome sequencing platformsHugo Y K Lam, Michael J Clark, Rui Chen, et al.
Nature Genetics|May 21, 2021
Computationally efficient whole-genome regression for quantitative and binary traitsJoelle Mbatchou, Leland Barnard, Joshua Backman, et al.
Genetic Epidemiology|November 3, 2025
Variant Classification Using Proteomics-Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target DiscoveryChristopher E Gillies, Joelle Mbatchou, Lukas Habegger, et al.
Science (New York, N.Y.)|March 20, 2010
Variation in transcription factor binding among humansMaya Kasowski, Fabian Grubert, Christopher Heffelfinger, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2010
Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencingJia Qian Wu, Lukas Habegger, Parinya Noisa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variantsBrenda Finucane, Matthew T Oetjens, Alicia Johns, et al.
Genome Biology|September 7, 2012
The GENCODE pseudogene resourceBaikang Pei, Cristina Sisu, Adam Frankish, et al.
Genome Biology|October 23, 2010
FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing dataAndrea Sboner, Lukas Habegger, Dorothee Pflueger, et al.
JAMA Psychiatry|July 23, 2020
Identification of Neuropsychiatric Copy Number Variants in a Health Care System PopulationChrista Lese Martin, Karen E Wain, Matthew T Oetjens, et al.
Nature Biotechnology|December 20, 2011
Performance comparison of whole-genome sequencing platformsHugo Y K Lam, Michael J Clark, Rui Chen, et al.
Nature Genetics|May 21, 2021
Computationally efficient whole-genome regression for quantitative and binary traitsJoelle Mbatchou, Leland Barnard, Joshua Backman, et al.
Genetic Epidemiology|November 3, 2025
Variant Classification Using Proteomics-Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target DiscoveryChristopher E Gillies, Joelle Mbatchou, Lukas Habegger, et al.
Science (New York, N.Y.)|March 20, 2010
Variation in transcription factor binding among humansMaya Kasowski, Fabian Grubert, Christopher Heffelfinger, et al.
Pageof 5