| Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer EP Murchison, OB Schulz-Trieglaff, Z Ning, LB Alexandrov, MJ Bauer, ... Cell 148 (4), 780-791, 2012 | 360 | 2012 |
| Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma CS Ross-Innes, J Becq, A Warren, RK Cheetham, H Northen, ... Nature genetics 47 (9), 1038-1046, 2015 | 303 | 2015 |
| Canvas: versatile and scalable detection of copy number variants E Roller, S Ivakhno, S Lee, T Royce, S Tanner Bioinformatics 32 (15), 2375-2377, 2016 | 174 | 2016 |
| CNAseg—a novel framework for identification of copy number changes in cancer from second-generation sequencing data S Ivakhno, T Royce, AJ Cox, DJ Evers, RK Cheetham, S Tavaré Bioinformatics 26 (24), 3051-3058, 2010 | 131 | 2010 |
| Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease AM Gross, SS Ajay, V Rajan, C Brown, K Bluske, NJ Burns, A Chawla, ... Genetics in Medicine 21 (5), 1121-1130, 2019 | 102 | 2019 |
| Development of a novel biosensor for the detection of arsenic in drinking water J Aleksic, F Bizzari, Y Cai, B Davidson, K De Mora, S Ivakhno, ... IET Synthetic biology 1 (1), 87-90, 2007 | 69 | 2007 |
| Non-linear dimensionality reduction of signaling networks S Ivakhno, JD Armstrong BMC systems biology 1, 1-17, 2007 | 19 | 2007 |
| Quantitative proteomics and its applications for systems biology S Ivakhno, A Kornelyuk Biochemistry (Moscow) 71, 1060-1072, 2006 | 18 | 2006 |
| Canvas SPW: calling de novo copy number variants in pedigrees S Ivakhno, E Roller, C Colombo, P Tedder, AJ Cox Bioinformatics 34 (3), 516-518, 2018 | 14 | 2018 |
| From functional genomics to systems biology: Meeting report based on the presentations at the 3rd EMBL Biennial Symposium 2006 (Heidelberg, Germany) S Ivakhno The FEBS Journal 274 (10), 2439-2448, 2007 | 11 | 2007 |
| CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray data S Ivakhno, S Tavaré Bioinformatics 26 (11), 1395-1402, 2010 | 10 | 2010 |
| tHapMix: simulating tumour samples through haplotype mixtures S Ivakhno, C Colombo, S Tanner, P Tedder, S Berri, AJ Cox Bioinformatics 33 (2), 280-282, 2017 | 9 | 2017 |
| Oesophageal Cancer Clinical and Molecular Stratification OCCAMS Study Group. Whole-genome sequencing provides new insights into the clonal architecture of Barrett’s esophagus … CS Ross-Innes, J Becq, A Warren, RK Cheetham, H Northen, ... Nat Genet 47 (9), 1038-46, 2015 | 8 | 2015 |
| Oesophageal Cancer Clinical and Molecular Stratification (OCCAMS) Study Group; Oesophageal Cancer Clinical and Molecular Stratification OCCAMS Study Group. Whole-genome … CS Ross-Innes, J Becq, A Warren, RK Cheetham, H Northen, ... Nat Genet 47 (9), 1038-1046, 2015 | 7 | 2015 |
| Arsenic biosenseor: a step further C French, J Nicholson, F Bizzari, J Aleksic, Y Cai, SL Seshasayee, ... BMC Systems Biology 1, 1-2, 2007 | 4 | 2007 |
| Copy number variants in clinical WGS: deployment and interpretation for rare and undiagnosed disease AM Gross, SS Ajay, V Rajan, C Brown, K Bluske, N Burns, A Chawla, ... bioRxiv, 245100, 2018 | 3 | 2018 |
| Oesophageal Cancer C, Molecular Stratification Study G, Oesophageal Cancer C and Molecular Stratification OSG. Whole-genome sequencing provides new insights into the clonal … CS Ross-Innes, J Becq, A Warren, RK Cheetham, H Northen, ... Nat Genet 47, 1038-1046, 2015 | 2 | 2015 |
| Versatile Identification of Copy Number Variants with Canvas S Ivakhno, E Roller Copy Number Variants: Methods and Protocols, 155-168, 2018 | | 2018 |
| Pancreatic cancer S Ivakhno, K Frese, S Tavare, C Iacobuzio-Donahue, D Tuveson Systems Biology of Cancer, 409-420, 2015 | | 2015 |
| Statistical framework for the analysis of copy number aberrations in high-throughput cancer genomic data S Ivakhno University of Cambridge, 2011 | | 2011 |
