Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Matthew Bainbridge

Showing results (11-20 of 36) with videos related to

Pageof 4
Sort By:
Biotechniques|July 10, 2008
Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencingRyan Morin, Matthew Bainbridge, Anthony Fejes, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in AutismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
Clinical Genetics|August 21, 2012
Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weaknessNeil A Hanchard, David R Murdock, Pilar L Magoulas, et al.
Cell Genomics|March 10, 2026
Long-read genome sequencing improves detection and functional interpretation of structural and repeat variants in autismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
The Journal of Pediatrics|July 7, 2024
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular PhenotypesErica Sanford Kobayashi, Nava Shaul Lotan, Yael Dinur Schejter, et al.
Fertility and Sterility|May 10, 2015
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermiaRanjith Ramasamy, M Emre Bakırcıoğlu, Cenk Cengiz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 10, 2025
Long-term follow-up of children who received rapid genomic sequencingErica Sanford Kobayashi, Laura E Tobin, Madison Arenchild, et al.
Nature Methods|June 15, 2007
Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencingGordon Robertson, Martin Hirst, Matthew Bainbridge, et al.
BMC Bioinformatics|January 31, 2014
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipelineJeffrey G Reid, Andrew Carroll, Narayanan Veeraraghavan, et al.
Nature Communications|December 10, 2025
Aberrant cytoplasmic localization of MLH1 characterizes a cell population that seeds breast cancer recurrenceAloran Mazumder, Jerry Dewitt, Elena Oropeza, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Biotechniques|July 10, 2008
Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencingRyan Morin, Matthew Bainbridge, Anthony Fejes, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in AutismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
Clinical Genetics|August 21, 2012
Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weaknessNeil A Hanchard, David R Murdock, Pilar L Magoulas, et al.
Cell Genomics|March 10, 2026
Long-read genome sequencing improves detection and functional interpretation of structural and repeat variants in autismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
The Journal of Pediatrics|July 7, 2024
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular PhenotypesErica Sanford Kobayashi, Nava Shaul Lotan, Yael Dinur Schejter, et al.
Fertility and Sterility|May 10, 2015
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermiaRanjith Ramasamy, M Emre Bakırcıoğlu, Cenk Cengiz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 10, 2025
Long-term follow-up of children who received rapid genomic sequencingErica Sanford Kobayashi, Laura E Tobin, Madison Arenchild, et al.
Nature Methods|June 15, 2007
Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencingGordon Robertson, Martin Hirst, Matthew Bainbridge, et al.
BMC Bioinformatics|January 31, 2014
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipelineJeffrey G Reid, Andrew Carroll, Narayanan Veeraraghavan, et al.
Nature Communications|December 10, 2025
Aberrant cytoplasmic localization of MLH1 characterizes a cell population that seeds breast cancer recurrenceAloran Mazumder, Jerry Dewitt, Elena Oropeza, et al.
Pageof 4