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Graham R Taylor

Showing results (11-20 of 35) with videos related to

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Journal of the National Comprehensive Cancer Network : JNCCN|March 10, 2016
BRAF Inhibition in BRAFV600E-Positive Anaplastic Thyroid CarcinomaAnnette M Lim, Graham R Taylor, Andrew Fellowes, et al.
Genomics|May 31, 2011
Illuminator, a desktop program for mutation detection using short-read clonal sequencingIan M Carr, Joanne E Morgan, Christine P Diggle, et al.
Human Mutation|February 10, 2015
AmpliVar: mutation detection in high-throughput sequence from amplicon-based librariesArthur L Hsu, Olga Kondrashova, Sebastian Lunke, et al.
Nature Biotechnology|September 10, 2011
Clarity and claims in variation/mutation databasingRaymond Dalgleish, William S Oetting, Arleen D Auerbach, et al.
The Journal of Molecular Diagnostics : JMD|January 14, 2012
Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumorsCaroline Conway, Rebecca Chalkley, Alec High, et al.
Human Mutation|February 4, 2010
Genetic diagnosis of familial breast cancer using clonal sequencingJoanne E Morgan, Ian M Carr, Eamonn Sheridan, et al.
Human Mutation|December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interfaceChristopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Human Mutation|March 25, 2009
Genetic and epigenetic analysis of recurrent hydatidiform moleBruce E Hayward, Michel De Vos, Nargese Talati, et al.
Human Mutation|August 24, 2012
Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnosticsPhilip A Chambers, Lucy F Stead, Joanne E Morgan, et al.
Human Mutation|April 5, 2013
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence dataIan M Carr, Joanne Morgan, Christopher Watson, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of the National Comprehensive Cancer Network : JNCCN|March 10, 2016
BRAF Inhibition in BRAFV600E-Positive Anaplastic Thyroid CarcinomaAnnette M Lim, Graham R Taylor, Andrew Fellowes, et al.
Genomics|May 31, 2011
Illuminator, a desktop program for mutation detection using short-read clonal sequencingIan M Carr, Joanne E Morgan, Christine P Diggle, et al.
Human Mutation|February 10, 2015
AmpliVar: mutation detection in high-throughput sequence from amplicon-based librariesArthur L Hsu, Olga Kondrashova, Sebastian Lunke, et al.
Nature Biotechnology|September 10, 2011
Clarity and claims in variation/mutation databasingRaymond Dalgleish, William S Oetting, Arleen D Auerbach, et al.
The Journal of Molecular Diagnostics : JMD|January 14, 2012
Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumorsCaroline Conway, Rebecca Chalkley, Alec High, et al.
Human Mutation|February 4, 2010
Genetic diagnosis of familial breast cancer using clonal sequencingJoanne E Morgan, Ian M Carr, Eamonn Sheridan, et al.
Human Mutation|December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interfaceChristopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Human Mutation|March 25, 2009
Genetic and epigenetic analysis of recurrent hydatidiform moleBruce E Hayward, Michel De Vos, Nargese Talati, et al.
Human Mutation|August 24, 2012
Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnosticsPhilip A Chambers, Lucy F Stead, Joanne E Morgan, et al.
Human Mutation|April 5, 2013
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence dataIan M Carr, Joanne Morgan, Christopher Watson, et al.
Pageof 4