Patrick S Tarpey

Patrick S Tarpey

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Patrick S Tarpey

Patrick S Tarpey

Publications by authors named "Patrick S Tarpey"

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Undifferentiated Sarcomas Develop through Distinct Evolutionary Pathways.

Cancer Cell 2019 Mar;35(3):441-456.e8

Research Department of Pathology, Cancer Institute, University College London, London WC1E 6BT, UK; Department of Cellular and Molecular Pathology, Royal National Orthopaedic Hospital NHS Trust, Stanmore, Middlesex HA7 4LP, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ccell.2019.02.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428691PMC
March 2019

cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data.

Curr Protoc Bioinformatics 2016 12 8;56:15.10.1-15.10.18. Epub 2016 Dec 8.

Cancer Genome Project, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.

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http://dx.doi.org/10.1002/cpbi.20DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097605PMC
December 2016

A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

Nat Commun 2015 Dec 9;6:10001. Epub 2015 Dec 9.

CNAG-CRG, Centre for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Baldiri i Reixac 4, 08028 Barcelona, Spain.

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http://dx.doi.org/10.1038/ncomms10001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682041PMC
December 2015

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.

Nat Genet 2015 Mar 2;47(3):257-62. Epub 2015 Feb 2.

1] Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada. [2] The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Ontario, Canada. [3] Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada. [4] Department of Pediatrics, University of Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/ng.3202DOI Listing
March 2015

Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.

Science 2014 Aug;345(6196):1251343

Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, UK.

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http://dx.doi.org/10.1126/science.1251343DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380235PMC
August 2014

What is next generation sequencing?

Arch Dis Child Educ Pract Ed 2013 Dec 28;98(6):236-8. Epub 2013 Aug 28.

Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, , Hinxton, Cambridgeshire, UK.

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http://dx.doi.org/10.1136/archdischild-2013-304340DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841808PMC
December 2013

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.

Nat Genet 2009 May 19;41(5):535-43. Epub 2009 Apr 19.

Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.

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http://dx.doi.org/10.1038/ng.367DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872007PMC
May 2009

Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders.

Neuromuscul Disord 2008 Aug 7;18(8):606-9. Epub 2008 Jul 7.

Institute for Neuromuscular Research, The Children's Hospital at Westmead, Sydney, Australia.

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http://dx.doi.org/10.1016/j.nmd.2008.05.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873833PMC
August 2008

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.

Hum Genet 2008 Jun 11;123(5):469-76. Epub 2008 Apr 11.

McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical School, 5323 Harry Hines Boulevard, Dallas, TX 75390-8591, USA.

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http://dx.doi.org/10.1007/s00439-008-0498-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714970PMC
June 2008

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.

Am J Hum Genet 2008 May 1;82(5):1150-7. Epub 2008 May 1.

Laboratoire de Génétique et Epigénétique des Maladies Métaboliques, Neurosensorielles et du Développement (INSERM U781), Université Paris Descartes, Hôpital Necker-Enfants Malades, F-75015 Paris, France.

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http://dx.doi.org/10.1016/j.ajhg.2008.03.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2427205PMC
May 2008

Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridization.

Genes Chromosomes Cancer 2005 Dec;44(4):384-91

The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

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http://doi.wiley.com/10.1002/gcc.20252
Publisher Site
http://dx.doi.org/10.1002/gcc.20252DOI Listing
December 2005

High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes.

Genes Chromosomes Cancer 2003 Jul;37(3):282-90

Department of Academic Haematology, Royal Free and University College School of Medicine, University College London, United Kingdom.

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http://dx.doi.org/10.1002/gcc.10215DOI Listing
July 2003