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Jonathan Sebat

Showing results (1-10 of 100) with videos related to

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Nature Genetics|September 5, 2007
Major changes in our DNA lead to major changes in our thinkingJonathan Sebat
The New England Journal of Medicine|March 11, 2026
Genetic Variation in Clinical CohortsJonathan Sebat
Cell|March 20, 2012
CNVs: harbingers of a rare variant revolution in psychiatric geneticsDheeraj Malhotra, Jonathan Sebat
Nature|May 19, 2012
Genetics: Fish heads and human diseaseDheeraj Malhotra, Jonathan Sebat
Nature Methods|July 4, 2012
forestSV: structural variant discovery through statistical learningJacob J Michaelson, Jonathan Sebat
Annual Review of Medicine|January 15, 2015
From de novo mutations to personalized therapeutic interventions in autismWilliam M Brandler, Jonathan Sebat
BMC Genomics|February 1, 2020
The effects of common structural variants on 3D chromatin structureOmar Shanta, Amina Noor, , et al.
Bioinformatics (Oxford, England)|January 5, 2018
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomesDanny Antaki, William M Brandler, Jonathan Sebat
Nucleic Acids Research|May 14, 2025
Cell type- and factor-specific nonsense-mediated RNA decayKun Tan, Jonathan Sebat, Miles F Wilkinson
Bioinformatics (Oxford, England)|April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNMAojie Lian, James Guevara, Kun Xia, et al.
Pageof 10

Showing results (1-10 of 100) with videos related to

Sort By:
Pageof 10
Nature Genetics|September 5, 2007
Major changes in our DNA lead to major changes in our thinkingJonathan Sebat
The New England Journal of Medicine|March 11, 2026
Genetic Variation in Clinical CohortsJonathan Sebat
Cell|March 20, 2012
CNVs: harbingers of a rare variant revolution in psychiatric geneticsDheeraj Malhotra, Jonathan Sebat
Nature|May 19, 2012
Genetics: Fish heads and human diseaseDheeraj Malhotra, Jonathan Sebat
Nature Methods|July 4, 2012
forestSV: structural variant discovery through statistical learningJacob J Michaelson, Jonathan Sebat
Annual Review of Medicine|January 15, 2015
From de novo mutations to personalized therapeutic interventions in autismWilliam M Brandler, Jonathan Sebat
BMC Genomics|February 1, 2020
The effects of common structural variants on 3D chromatin structureOmar Shanta, Amina Noor, , et al.
Bioinformatics (Oxford, England)|January 5, 2018
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomesDanny Antaki, William M Brandler, Jonathan Sebat
Nucleic Acids Research|May 14, 2025
Cell type- and factor-specific nonsense-mediated RNA decayKun Tan, Jonathan Sebat, Miles F Wilkinson
Bioinformatics (Oxford, England)|April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNMAojie Lian, James Guevara, Kun Xia, et al.
Pageof 10