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

Graham Bignell

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Bioinformatics (Oxford, England)|May 21, 2005
CGHAnalyzer: a stand-alone software package for cancer genome analysis using array-based DNA copy number dataAdam A Margolin, Joel Greshock, Tara L Naylor, et al.
Biostatistics (Oxford, England)|October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer dataChris D Greenman, Graham Bignell, Adam Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 12, 2005
A survey of homozygous deletions in human cancer genomesCharles Cox, Graham Bignell, Chris Greenman, et al.
Cancer Research|December 13, 2017
Transcription Factor Activities Enhance Markers of Drug Sensitivity in CancerLuz Garcia-Alonso, Francesco Iorio, Angela Matchan, et al.
Genomics|January 13, 2006
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparisonHelen Davies, Ed Dicks, Philip Stephens, et al.
Cancer Cell|April 9, 2008
Feedback circuit among INK4 tumor suppressors constrains human glioblastoma developmentRuprecht Wiedemeyer, Cameron Brennan, Timothy P Heffernan, et al.
Nature Communications|May 18, 2019
Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screeningGabriele Picco, Elisabeth D Chen, Luz Garcia Alonso, et al.
Genome Research|February 10, 2017
Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutationsJonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
American Journal of Human Genetics|June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationPatrick Tarpey, Josep Parnau, Matthew Blow, et al.
Scientific Reports|September 12, 2018
An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signaturesGrace Collord, Patrick Tarpey, Natalja Kurbatova, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|May 21, 2005
CGHAnalyzer: a stand-alone software package for cancer genome analysis using array-based DNA copy number dataAdam A Margolin, Joel Greshock, Tara L Naylor, et al.
Biostatistics (Oxford, England)|October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer dataChris D Greenman, Graham Bignell, Adam Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 12, 2005
A survey of homozygous deletions in human cancer genomesCharles Cox, Graham Bignell, Chris Greenman, et al.
Cancer Research|December 13, 2017
Transcription Factor Activities Enhance Markers of Drug Sensitivity in CancerLuz Garcia-Alonso, Francesco Iorio, Angela Matchan, et al.
Genomics|January 13, 2006
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparisonHelen Davies, Ed Dicks, Philip Stephens, et al.
Cancer Cell|April 9, 2008
Feedback circuit among INK4 tumor suppressors constrains human glioblastoma developmentRuprecht Wiedemeyer, Cameron Brennan, Timothy P Heffernan, et al.
Nature Communications|May 18, 2019
Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screeningGabriele Picco, Elisabeth D Chen, Luz Garcia Alonso, et al.
Genome Research|February 10, 2017
Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutationsJonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
American Journal of Human Genetics|June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationPatrick Tarpey, Josep Parnau, Matthew Blow, et al.
Scientific Reports|September 12, 2018
An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signaturesGrace Collord, Patrick Tarpey, Natalja Kurbatova, et al.
Pageof 2