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Charlotte G Cole

Showing results (1-10 of 9) with videos related to

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Nature Reviews. Cancer|October 8, 2018
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancersZbyslaw Sondka, Sally Bamford, Charlotte G Cole, et al.
Genome Research|January 17, 2003
Reevaluating human gene annotation: a second-generation analysis of chromosome 22John E Collins, Melanie E Goward, Charlotte G Cole, et al.
Genome Biology|May 15, 2008
Finishing the finished human chromosome 22 sequenceCharlotte G Cole, Owen T McCann, John E Collins, et al.
Human Genetics|March 10, 2004
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative geneJoanne E Langan, Charlotte G Cole, Elisabeth J Huckle, et al.
Genome Biology|October 6, 2004
A genome annotation-driven approach to cloning the human ORFeomeJohn E Collins, Charmain L Wright, Carol A Edwards, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2011
Data mining using the Catalogue of Somatic Mutations in Cancer BioMartRebecca Shepherd, Simon A Forbes, David Beare, et al.
Nucleic Acids Research|December 1, 2016
COSMIC: somatic cancer genetics at high-resolutionSimon A Forbes, David Beare, Harry Boutselakis, et al.
Nucleic Acids Research|October 30, 2018
COSMIC: the Catalogue Of Somatic Mutations In CancerJohn G Tate, Sally Bamford, Harry C Jubb, et al.
Nature|March 18, 2005
The DNA sequence of the human X chromosomeMark T Ross, Darren V Grafham, Alison J Coffey, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Nature Reviews. Cancer|October 8, 2018
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancersZbyslaw Sondka, Sally Bamford, Charlotte G Cole, et al.
Genome Research|January 17, 2003
Reevaluating human gene annotation: a second-generation analysis of chromosome 22John E Collins, Melanie E Goward, Charlotte G Cole, et al.
Genome Biology|May 15, 2008
Finishing the finished human chromosome 22 sequenceCharlotte G Cole, Owen T McCann, John E Collins, et al.
Human Genetics|March 10, 2004
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative geneJoanne E Langan, Charlotte G Cole, Elisabeth J Huckle, et al.
Genome Biology|October 6, 2004
A genome annotation-driven approach to cloning the human ORFeomeJohn E Collins, Charmain L Wright, Carol A Edwards, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2011
Data mining using the Catalogue of Somatic Mutations in Cancer BioMartRebecca Shepherd, Simon A Forbes, David Beare, et al.
Nucleic Acids Research|December 1, 2016
COSMIC: somatic cancer genetics at high-resolutionSimon A Forbes, David Beare, Harry Boutselakis, et al.
Nucleic Acids Research|October 30, 2018
COSMIC: the Catalogue Of Somatic Mutations In CancerJohn G Tate, Sally Bamford, Harry C Jubb, et al.
Nature|March 18, 2005
The DNA sequence of the human X chromosomeMark T Ross, Darren V Grafham, Alison J Coffey, et al.
Pageof 1