Bogdan Pasaniuc

According to our database1, Bogdan Pasaniuc authored at least 32 papers between 2006 and 2021.

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In proceedings 
PhD thesis 


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Leveraging eQTLs to identify individual-level tissue of interest for a complex trait.
PLoS Comput. Biol., 2021

Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits.
PLoS Comput. Biol., 2021

Pipeline for Analyzing Activity of Metabolic Pathways in Planktonic Communities Using Metatranscriptomic Data.
J. Comput. Biol., 2021

A two-step approach to testing overall effect of gene-environment interaction for multiple phenotypes.
Bioinform., 2021

A Scalable Method for Estimating the Regional Polygenicity of Complex Traits.
Proceedings of the Research in Computational Molecular Biology, 2020

Estimating Enzyme Participation in Metabolic Pathways for Microbial Communities from RNA-seq Data.
Proceedings of the Bioinformatics Research and Applications - 16th International Symposium, 2020

RAISS: robust and accurate imputation from summary statistics.
Bioinform., 2019

Scalable Multi-component Linear Mixed Models with Application to SNP Heritability Estimation.
Proceedings of the Research in Computational Molecular Biology, 2019

A unifying framework for joint trait analysis under a non-infinitesimal model.
Bioinform., 2018

A Bayesian framework for multiple trait colocalization from summary association statistics.
Bioinform., 2018

Improved methods for multi-trait fine mapping of pleiotropic risk loci.
Bioinform., 2017

Enhanced methods to detect haplotypic effects on gene expression.
Bioinform., 2017

A Spatial Haplotype Copying Model with Applications to Genotype Imputation.
J. Comput. Biol., 2015

A multivariate Bernoulli model to predict DNaseI hypersensitivity status from haplotype data.
Bioinform., 2015

Identification of causal genes for complex traits.
Bioinform., 2015

Enhanced Methods for Local Ancestry Assignment in Sequenced Admixed Individuals.
PLoS Comput. Biol., 2014

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment.
Bioinform., 2014

A Spatial-Aware Haplotype Copying Model with Applications to Genotype Imputation.
Proceedings of the Research in Computational Molecular Biology, 2014

Identifying causal variants at loci with multiple signals of association.
Proceedings of the 5th ACM Conference on Bioinformatics, 2014

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data.
Bioinform., 2013

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation.
Bioinform., 2013

Analysis of case-control association studies with known risk variants.
Bioinform., 2012

Fast and accurate inference of local ancestry in Latino populations.
Bioinform., 2012

Accurate Estimation of Expression Levels of Homologous Genes in RNA-seq Experiments.
J. Comput. Biol., 2011

Optimal Testing of Digital Microfluidic Biochips.
INFORMS J. Comput., 2011

Genotyping common and rare variation using overlapping pool sequencing.
BMC Bioinform., 2011

GEDI: Scalable Algorithms for Genotype Error Detection and Imputation
CoRR, 2009

Inference of locus-specific ancestry in closely related populations.
Bioinform., 2009

Imputation-Based Local Ancestry Inference in Admixed Populations.
Proceedings of the Bioinformatics Research and Applications, 5th International Symposium, 2009

Highly Scalable Genotype Phasing by Entropy Minimization.
IEEE ACM Trans. Comput. Biol. Bioinform., 2008

Genotype Error Detection Using Hidden Markov Models of Haplotype Diversity.
J. Comput. Biol., 2008

Highly Scalable Genotype Phasing by Entropy Minimization.
Proceedings of the 28th International Conference of the IEEE Engineering in Medicine and Biology Society, 2006