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Annals of Human Genetics
|
December 2, 2010
Importance measures for epistatic interactions in case-parent trios
Holger 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 studies
Cristian 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 arrays
Robert B Scharpf, Giovanni Parmigiani, Jonathan Pevsner, et al.
Eupa Open Proteomics
|
March 31, 2015
Detecting Significant Changes in Protein Abundance
Kai Kammers, Robert N Cole, Calvin Tiengwe, et al.
Genetic Epidemiology
|
September 21, 2006
Imputation methods to improve inference in SNP association studies
James Y Dai, Ingo Ruczinski, Michael LeBlanc, et al.
Bioinformatics (Oxford, England)
|
January 6, 2007
SNPchip: R classes and methods for SNP array data
Robert B Scharpf, Jason C Ting, Jonathan Pevsner, et al.
Bioinformatics (Oxford, England)
|
December 1, 2018
Detection of rare disease variants in extended pedigrees using RVS
Thomas 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 sequence
Samir Oubninte, Ingo Ruczinski, Lisa R Yanek, et al.
Bioinformatics (Oxford, England)
|
August 12, 2022
Detecting and quantifying antibody reactivity in PhIP-Seq data with BEER
Athena 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 pipelines
Seth R Berke, Kanika Kanchan, Mary L Marazita, et al.
Page
of 21
Search research articles
Search
Showing results (11-20 of 202) with videos related to
Sort By:
Page
of 21
Annals of Human Genetics
|
December 2, 2010
Importance measures for epistatic interactions in case-parent trios
Holger 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 studies
Cristian 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 arrays
Robert B Scharpf, Giovanni Parmigiani, Jonathan Pevsner, et al.
Eupa Open Proteomics
|
March 31, 2015
Detecting Significant Changes in Protein Abundance
Kai Kammers, Robert N Cole, Calvin Tiengwe, et al.
Genetic Epidemiology
|
September 21, 2006
Imputation methods to improve inference in SNP association studies
James Y Dai, Ingo Ruczinski, Michael LeBlanc, et al.
Bioinformatics (Oxford, England)
|
January 6, 2007
SNPchip: R classes and methods for SNP array data
Robert B Scharpf, Jason C Ting, Jonathan Pevsner, et al.
Bioinformatics (Oxford, England)
|
December 1, 2018
Detection of rare disease variants in extended pedigrees using RVS
Thomas 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 sequence
Samir Oubninte, Ingo Ruczinski, Lisa R Yanek, et al.
Bioinformatics (Oxford, England)
|
August 12, 2022
Detecting and quantifying antibody reactivity in PhIP-Seq data with BEER
Athena 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 pipelines
Seth R Berke, Kanika Kanchan, Mary L Marazita, et al.
Page
of 21