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Bioinformatics (Oxford, England)|April 21, 2010
CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray dataSergii Ivakhno, Simon TavaréBioinformatics (Oxford, England)|October 23, 2010
CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing dataSergii Ivakhno, Tom Royce, Anthony J Cox, et al.Methods in Molecular Biology (Clifton, N.J.)|July 25, 2018
Versatile Identification of Copy Number Variants with CanvasSergii Ivakhno, Eric RollerBMC Systems Biology|June 15, 2007
Non-linear dimensionality reduction of signaling networksSergii Ivakhno, J Douglas ArmstrongBioinformatics (Oxford, England)|May 7, 2016
Canvas: versatile and scalable detection of copy number variantsEric Roller, Sergii Ivakhno, Steve Lee, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 20, 2025
Birth and death processes in phylogenetics and population geneticsSimon TavaréBioinformatics (Oxford, England)|October 14, 2017
Canvas SPW: calling de novo copy number variants in pedigreesSergii Ivakhno, Eric Roller, Camilla Colombo, et al.Bioinformatics (Oxford, England)|September 9, 2016
tHapMix: simulating tumour samples through haplotype mixturesSergii Ivakhno, Camilla Colombo, Stephen Tanner, et al.Cell Cycle (Georgetown, Tex.)|April 4, 2006
Counting divisions in a human somatic cell tree: how, what and why?Darryl Shibata, Simon TavaréPageof 16