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Ingo Ruczinski

Showing results (11-20 of 202) with videos related to

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Annals of Human Genetics|December 2, 2010
Importance measures for epistatic interactions in case-parent triosHolger Schwender, Katherine Bowers, M Daniele Fallin, et al.
BMC Genomics|September 2, 2008
Haplotype block partitioning as a tool for dimensionality reduction in SNP association studiesCristian Pattaro, Ingo Ruczinski, Danièle M Fallin, et al.
The Annals of Applied Statistics|July 18, 2009
Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arraysRobert B Scharpf, Giovanni Parmigiani, Jonathan Pevsner, et al.
Eupa Open Proteomics|March 31, 2015
Detecting Significant Changes in Protein AbundanceKai Kammers, Robert N Cole, Calvin Tiengwe, et al.
Genetic Epidemiology|September 21, 2006
Imputation methods to improve inference in SNP association studiesJames Y Dai, Ingo Ruczinski, Michael LeBlanc, et al.
Bioinformatics (Oxford, England)|January 6, 2007
SNPchip: R classes and methods for SNP array dataRobert B Scharpf, Jason C Ting, Jonathan Pevsner, et al.
Bioinformatics (Oxford, England)|December 1, 2018
Detection of rare disease variants in extended pedigrees using RVSThomas Sherman, Jack Fu, Robert B Scharpf, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
The reliability and accuracy of recombination inferred by Shapeit2 duoHMM on whole genome sequenceSamir Oubninte, Ingo Ruczinski, Lisa R Yanek, et al.
Bioinformatics (Oxford, England)|August 12, 2022
Detecting and quantifying antibody reactivity in PhIP-Seq data with BEERAthena Chen, Kai Kammers, H Benjamin Larman, et al.
Plos Computational Biology|July 2, 2025
Fundamentals of FAIR biomedical data analyses in the cloud using custom pipelinesSeth R Berke, Kanika Kanchan, Mary L Marazita, et al.
Pageof 21

Showing results (11-20 of 202) with videos related to

Sort By:
Pageof 21
Annals of Human Genetics|December 2, 2010
Importance measures for epistatic interactions in case-parent triosHolger Schwender, Katherine Bowers, M Daniele Fallin, et al.
BMC Genomics|September 2, 2008
Haplotype block partitioning as a tool for dimensionality reduction in SNP association studiesCristian Pattaro, Ingo Ruczinski, Danièle M Fallin, et al.
The Annals of Applied Statistics|July 18, 2009
Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arraysRobert B Scharpf, Giovanni Parmigiani, Jonathan Pevsner, et al.
Eupa Open Proteomics|March 31, 2015
Detecting Significant Changes in Protein AbundanceKai Kammers, Robert N Cole, Calvin Tiengwe, et al.
Genetic Epidemiology|September 21, 2006
Imputation methods to improve inference in SNP association studiesJames Y Dai, Ingo Ruczinski, Michael LeBlanc, et al.
Bioinformatics (Oxford, England)|January 6, 2007
SNPchip: R classes and methods for SNP array dataRobert B Scharpf, Jason C Ting, Jonathan Pevsner, et al.
Bioinformatics (Oxford, England)|December 1, 2018
Detection of rare disease variants in extended pedigrees using RVSThomas Sherman, Jack Fu, Robert B Scharpf, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
The reliability and accuracy of recombination inferred by Shapeit2 duoHMM on whole genome sequenceSamir Oubninte, Ingo Ruczinski, Lisa R Yanek, et al.
Bioinformatics (Oxford, England)|August 12, 2022
Detecting and quantifying antibody reactivity in PhIP-Seq data with BEERAthena Chen, Kai Kammers, H Benjamin Larman, et al.
Plos Computational Biology|July 2, 2025
Fundamentals of FAIR biomedical data analyses in the cloud using custom pipelinesSeth R Berke, Kanika Kanchan, Mary L Marazita, et al.
Pageof 21