PubMed ID |
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25790038 |
Publish Date |
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2015 Mar |
Journal |
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Nature Communications |
Species |
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Homo sapiens |
Disease Type |
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Renal cancer |
Technology |
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Next Generation Sequencing |
Case Number |
|
1 |
Raw Data |
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EBI: PRJEB7875, ERP008861 |
Title |
|
Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution |
Authors |
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Kovac M, Navas C, Horswell S, Salm M, Bardella C, Rowan A, Stares M, Castro-Giner F, Fisher R, de Bruin EC, Kovacova M, Gorman M, Makino S, Williams J, Jaeger E, Jones A, Howarth K, Larkin J, Pickering L, Gore M, Nicol DL, Hazell S, Stamp G, O'Brien T, Challacombe B, Matthews N, Phillimore B, Begum S, Rabinowitz A, Varela I, Chandra A, Horsfield C, Polson A, Tran M, Bhatt R, Terracciano L, Eppenberger-Castori S, Protheroe A, Maher E, El Bahrawy M, Fleming S, Ratcliffe P, Heinimann K, Swanton C, Tomlinson I |
Affiliation |
|
Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, Nuffield Department of Clinical Medicine, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK |
Chromothripsis Definition |
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Close-by breakpoints: >=200 Copy number states: 3 Fragments random joining: NA |
Download |
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Study Data File |
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Chromothripsis Cases |
P09 |
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Case ID: |
P09 |
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Chromosome: | 2 |
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Disease type: |
Renal cancer |
|
Technology: |
Next Generation Sequencing |
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Platform: |
Complete Genomics |
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Affected Gene: |
Gene List |
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Download: |
Links File |
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