Search research articles
Contact Us
Filters
Showing results (1-10 of 100) with videos related to
Page
of 10
Sort By:
Nature Genetics
|
September 5, 2007
Major changes in our DNA lead to major changes in our thinking
Jonathan Sebat
The New England Journal of Medicine
|
March 11, 2026
Genetic Variation in Clinical Cohorts
Jonathan Sebat
Cell
|
March 20, 2012
CNVs: harbingers of a rare variant revolution in psychiatric genetics
Dheeraj Malhotra, Jonathan Sebat
Nature
|
May 19, 2012
Genetics: Fish heads and human disease
Dheeraj Malhotra, Jonathan Sebat
Nature Methods
|
July 4, 2012
forestSV: structural variant discovery through statistical learning
Jacob J Michaelson, Jonathan Sebat
Annual Review of Medicine
|
January 15, 2015
From de novo mutations to personalized therapeutic interventions in autism
William M Brandler, Jonathan Sebat
BMC Genomics
|
February 1, 2020
The effects of common structural variants on 3D chromatin structure
Omar Shanta, Amina Noor, , et al.
Bioinformatics (Oxford, England)
|
January 5, 2018
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes
Danny Antaki, William M Brandler, Jonathan Sebat
Nucleic Acids Research
|
May 14, 2025
Cell type- and factor-specific nonsense-mediated RNA decay
Kun Tan, Jonathan Sebat, Miles F Wilkinson
Bioinformatics (Oxford, England)
|
April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNM
Aojie Lian, James Guevara, Kun Xia, et al.
Page
of 10
Search research articles
Search
Showing results (1-10 of 100) with videos related to
Sort By:
Page
of 10
Nature Genetics
|
September 5, 2007
Major changes in our DNA lead to major changes in our thinking
Jonathan Sebat
The New England Journal of Medicine
|
March 11, 2026
Genetic Variation in Clinical Cohorts
Jonathan Sebat
Cell
|
March 20, 2012
CNVs: harbingers of a rare variant revolution in psychiatric genetics
Dheeraj Malhotra, Jonathan Sebat
Nature
|
May 19, 2012
Genetics: Fish heads and human disease
Dheeraj Malhotra, Jonathan Sebat
Nature Methods
|
July 4, 2012
forestSV: structural variant discovery through statistical learning
Jacob J Michaelson, Jonathan Sebat
Annual Review of Medicine
|
January 15, 2015
From de novo mutations to personalized therapeutic interventions in autism
William M Brandler, Jonathan Sebat
BMC Genomics
|
February 1, 2020
The effects of common structural variants on 3D chromatin structure
Omar Shanta, Amina Noor, , et al.
Bioinformatics (Oxford, England)
|
January 5, 2018
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes
Danny Antaki, William M Brandler, Jonathan Sebat
Nucleic Acids Research
|
May 14, 2025
Cell type- and factor-specific nonsense-mediated RNA decay
Kun Tan, Jonathan Sebat, Miles F Wilkinson
Bioinformatics (Oxford, England)
|
April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNM
Aojie Lian, James Guevara, Kun Xia, et al.
Page
of 10