Farhad Hormozdiari

According to our database1, Farhad Hormozdiari authored at least 27 papers between 2007 and 2020.

Collaborative distances:



In proceedings 
PhD thesis 


On csauthors.net:


Underspecification Presents Challenges for Credibility in Modern Machine Learning.
CoRR, 2020

Identifying Causal Variants by Fine Mapping Across Multiple Studies.
Proceedings of the Research in Computational Molecular Biology, 2020

Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.
J. Comput. Biol., 2019

The impact of rare variation on gene expression across tissues.
Nat., 2017

Using genomic annotations increases statistical power to detect eGenes.
Bioinform., 2016

The Second Decade of the International Conference on Research in Computational Molecular Biology (RECOMB).
Proceedings of the Research in Computational Molecular Biology - 20th Annual Conference, 2016

HapIso: An Accurate Method for the Haplotype-Specific Isoforms Reconstruction from Long Single-Molecule Reads.
Proceedings of the Bioinformatics Research and Applications - 12th International Symposium, 2016

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

Memory efficient assembly of human genome.
J. Bioinform. Comput. Biol., 2015

PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling.
BMC Bioinform., 2015

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

mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications.
Nucleic Acids Res., 2014

Privacy preserving protocol for detecting genetic relatives using rare variants.
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

CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping.
J. Comput. Biol., 2013

eALPS: Estimating Abundance Levels in Pooled Sequencing Using Available Genotyping Data.
J. Comput. Biol., 2013

Accelerating read mapping with FastHASH.
BMC Genom., 2013

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

Sensitive and fast mapping of di-base encoded reads.
Bioinform., 2012

Efficient genotyping of individuals using overlapping pool sequencing and imputation.
Proceedings of the Conference Record of the Forty Sixth Asilomar Conference on Signals, 2012

Assembly of non-unique insertion content using next-generation sequencing.
BMC Bioinform., 2011

Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions.
Bioinform., 2011

Applicability Domains for Classification Problems: Benchmarking of Distance to Models for Ames Mutagenicity Set.
J. Chem. Inf. Model., 2010

Analysis of the Impact of Wavelength Converters on Contention Resolution in Optical Burst Switching.
Proceedings of the Second Asia International Conference on Modelling and Simulation, 2008

Mathematical Analysis of Delay Line to Wavelength Allocation Algorithmsin Optical Networks.
Proceedings of the 15th International Symposium on Modeling, 2007

Flows with Bounded Waiting Time in Networked and Distributed Systems.
Proceedings of the First Asia International Conference on Modelling and Simulation, 2007