Assessing the Impact of Non-Differential Genotyping Errors on Rare Variant Tests of Association

Por Powers, Scott, Gopalakrishnan, Shyam, Tintle, Nathan
Publicado em 2011

Optimal methods for using posterior probabilities in association testing

Por Liu, Keli, Luedtke, Alexander, Tintle, Nathan
Publicado em 2013

Pathway analysis approaches for rare and common variants: Insights from GAW18

Por Aslibekyan, Stella, Almeida, Marcio, Tintle, Nathan
Publicado no Genet Epidemiol (2014)

Comparing machine learning and logistic regression methods for predicting hypertension using a combination of gene expression and next-generation sequencing data

Por Held, Elizabeth, Cape, Joshua, Tintle, Nathan
Publicado no BMC Proc (2016)

Evaluating the concordance between sequencing, imputation and microarray genotype calls in the GAW18 data

Por Rogers, Ally, Beck, Andrew, Tintle, Nathan L
Publicado em 2014

Assessing the Impact of Differential Genotyping Errors on Rare Variant Tests of Association

Por Mayer-Jochimsen, Morgan, Fast, Shannon, Tintle, Nathan L.
Publicado em 2013

Evaluating the impact of genotype errors on rare variant tests of association

Por Cook, Kaitlyn, Benitez, Alejandra, Fu, Casey, Tintle, Nathan
Publicado em 2014

Risk Factors for Physical Violence against Partners in the U.S.

Por O'Leary, K. Daniel, Tintle, Nathan, Bromet, Evelyn
Publicado no Psychol Violence (2014)

A POWERFUL METHOD FOR INCLUDING GENOTYPE UNCERTAINTY IN TESTS OF HARDY-WEINBERG EQUILIBRIUM

Por Beck, Andrew, Luedtke, Alexander, Liu, Keli, Tintle, Nathan
Publicado no Pac Symp Biocomput (2016)

IMPROVED PERFORMANCE OF GENE SET ANALYSIS ON GENOME-WIDE TRANSCRIPTOMICS DATA WHEN USING GENE ACTIVITY STATE ESTIMATES

Por Kamp, Thomas, Adams, Micah, Disselkoen, Craig, Tintle, Nathan
Publicado no Pac Symp Biocomput (2016)

The cost effectiveness of duplicate genotyping for testing genetic association

Por Tintle, Nathan, Gordon, Derek, Van Bruggen, Dirk, Finch, Stephen
Publicado em 2009

Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16

Por Tintle, Nathan L, Borchers, Bryce, Brown, Marshall, Bekmetjev, Airat
Publicado em 2009

A geometric framework for evaluating rare variant tests of association

Por Liu, Keli, Fast, Shannon, Zawistowski, Matthew, Tintle, Nathan L.
Publicado em 2013

Prolonged fatigue in Ukraine and the United States: Prevalence and risk factors

Por Friedberg, Fred, Tintle, Nathan, Clark, Jake, Bromet, Evelyn J.
Publicado no Fatigue (2014)

Identification of Genetic Association of Multiple Rare Variants Using Collapsing Methods

Por Sun, Yan V., Sung, Yun Ju, Tintle, Nathan, Ziegler, Andreas
Publicado em 2011

Assessing Methods for Assigning SNPs to Genes in Gene-Based Tests of Association Using Common Variants

Por Petersen, Ashley, Alvarez, Carolina, DeClaire, Scott, Tintle, Nathan L.
Publicado em 2013

A multistep approach to single nucleotide polymorphism–set analysis: an evaluation of power and type I error of gene-based tests of association after pathway-based association test...

Por Valcarcel, Alessandra, Grinde, Kelsey, Cook, Kaitlyn, Green, Alden, Tintle, Nathan
Publicado no BMC Proc (2016)

A general method for combining different family-based rare-variant tests of association to improve power and robustness of a wide range of genetic architectures

Por Green, Alden, Cook, Kaitlyn, Grinde, Kelsey, Valcarcel, Alessandra, Tintle, Nathan
Publicado no BMC Proc (2016)

On the value of Mendelian laws of segregation in families: data quality control, imputation and beyond

Por Blue, Elizabeth Marchani, Sun, Lei, Tintle, Nathan L., Wijsman, Ellen M.
Publicado em 2014

Cautions about the reliability of pairwise gene correlations based on expression data

Por Powers, Scott, DeJongh, Matt, Best, Aaron A., Tintle, Nathan L.
Publicado no Front Microbiol (2015)