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Sergii Ivakhno

Showing results (1-10 of 11) with videos related to

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The FEBS Journal|April 25, 2007
From functional genomics to systems biologySergii Ivakhno
Methods in Molecular Biology (Clifton, N.J.)|July 25, 2018
Versatile Identification of Copy Number Variants with CanvasSergii Ivakhno, Eric Roller
Bioinformatics (Oxford, England)|April 21, 2010
CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray dataSergii Ivakhno, Simon Tavaré
BMC Systems Biology|June 15, 2007
Non-linear dimensionality reduction of signaling networksSergii Ivakhno, J Douglas Armstrong
Bioinformatics (Oxford, England)|May 7, 2016
Canvas: versatile and scalable detection of copy number variantsEric Roller, Sergii Ivakhno, Steve Lee, et al.
Bioinformatics (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.
Bioinformatics (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.
Nature Genetics|July 21, 2015
Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinomaCaryn S Ross-Innes, Jennifer Becq, Andrew Warren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The FEBS Journal|April 25, 2007
From functional genomics to systems biologySergii Ivakhno
Methods in Molecular Biology (Clifton, N.J.)|July 25, 2018
Versatile Identification of Copy Number Variants with CanvasSergii Ivakhno, Eric Roller
Bioinformatics (Oxford, England)|April 21, 2010
CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray dataSergii Ivakhno, Simon Tavaré
BMC Systems Biology|June 15, 2007
Non-linear dimensionality reduction of signaling networksSergii Ivakhno, J Douglas Armstrong
Bioinformatics (Oxford, England)|May 7, 2016
Canvas: versatile and scalable detection of copy number variantsEric Roller, Sergii Ivakhno, Steve Lee, et al.
Bioinformatics (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.
Bioinformatics (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.
Nature Genetics|July 21, 2015
Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinomaCaryn S Ross-Innes, Jennifer Becq, Andrew Warren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Pageof 2