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 N Bainbridge

Showing results (31-40 of 67) with videos related to

Pageof 7
Sort By:
Genome Biology|June 23, 2010
Whole exome capture in solution with 3 Gbp of dataMatthew N Bainbridge, Min Wang, Daniel L Burgess, et al.
Science Advances|June 30, 2023
Molecular portraits of cell cycle checkpoint kinases in cancer evolution, progression, and treatment responsivenessElena Oropeza, Sinem Seker, Sabrina Carrel, et al.
Source Code for Biology and Medicine|June 23, 2016
SV-STAT accurately detects structural variation via alignment to reference-based assembliesCaleb F Davis, Deborah I Ritter, David A Wheeler, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Neuro-Oncology|October 18, 2017
Molecular subtyping of tumors from patients with familial gliomaVanessa Y Ruiz, Corinne E Praska, Georgina Armstrong, et al.
BMC Genomics|October 3, 2006
Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approachMatthew N Bainbridge, René L Warren, Martin Hirst, et al.
Science Translational Medicine|June 17, 2011
Whole-genome sequencing for optimized patient managementMatthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
NPJ Genomic Medicine|April 13, 2018
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalizationLauge Farnaes, Amber Hildreth, Nathaly M Sweeney, et al.
BMC Medical Genomics|February 23, 2012
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genesLuca A Lotta, Mark Wang, Jin Yu, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Genome Biology|June 23, 2010
Whole exome capture in solution with 3 Gbp of dataMatthew N Bainbridge, Min Wang, Daniel L Burgess, et al.
Science Advances|June 30, 2023
Molecular portraits of cell cycle checkpoint kinases in cancer evolution, progression, and treatment responsivenessElena Oropeza, Sinem Seker, Sabrina Carrel, et al.
Source Code for Biology and Medicine|June 23, 2016
SV-STAT accurately detects structural variation via alignment to reference-based assembliesCaleb F Davis, Deborah I Ritter, David A Wheeler, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Neuro-Oncology|October 18, 2017
Molecular subtyping of tumors from patients with familial gliomaVanessa Y Ruiz, Corinne E Praska, Georgina Armstrong, et al.
BMC Genomics|October 3, 2006
Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approachMatthew N Bainbridge, René L Warren, Martin Hirst, et al.
Science Translational Medicine|June 17, 2011
Whole-genome sequencing for optimized patient managementMatthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
NPJ Genomic Medicine|April 13, 2018
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalizationLauge Farnaes, Amber Hildreth, Nathaly M Sweeney, et al.
BMC Medical Genomics|February 23, 2012
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genesLuca A Lotta, Mark Wang, Jin Yu, et al.
Pageof 7