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Patrick S Tarpey

Showing results (1-10 of 55) with videos related to

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Archives of Disease in Childhood. Education and Practice Edition|August 30, 2013
What is next generation sequencing?Sam Behjati, Patrick S Tarpey
Genes, Chromosomes & Cancer|May 22, 2003
High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probesAlistair G Reid, Patrick S Tarpey, Ellie P Nacheva
Genes, Chromosomes & Cancer|August 20, 2005
Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridizationEleanor J Davison, Patrick S Tarpey, Heike Fiegler, et al.
Current Protocols in Bioinformatics|December 9, 2016
cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS DataDavid Jones, Keiran M Raine, Helen Davies, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disordersRachel A Peat, Jozef Gécz, Justin R Fallon, et al.
European Journal of Human Genetics : EJHG|October 15, 2009
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlationSinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, et al.
American Journal of Human Genetics|May 6, 2008
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardationFlorence Molinari, François Foulquier, Patrick S Tarpey, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Natural history of Christianson syndromeRichard J Schroer, Kenton R Holden, Patrick S Tarpey, et al.
Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.
Nature Genetics|October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordomaNischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Archives of Disease in Childhood. Education and Practice Edition|August 30, 2013
What is next generation sequencing?Sam Behjati, Patrick S Tarpey
Genes, Chromosomes & Cancer|May 22, 2003
High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probesAlistair G Reid, Patrick S Tarpey, Ellie P Nacheva
Genes, Chromosomes & Cancer|August 20, 2005
Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridizationEleanor J Davison, Patrick S Tarpey, Heike Fiegler, et al.
Current Protocols in Bioinformatics|December 9, 2016
cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS DataDavid Jones, Keiran M Raine, Helen Davies, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disordersRachel A Peat, Jozef Gécz, Justin R Fallon, et al.
European Journal of Human Genetics : EJHG|October 15, 2009
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlationSinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, et al.
American Journal of Human Genetics|May 6, 2008
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardationFlorence Molinari, François Foulquier, Patrick S Tarpey, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Natural history of Christianson syndromeRichard J Schroer, Kenton R Holden, Patrick S Tarpey, et al.
Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.
Nature Genetics|October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordomaNischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.
Pageof 6