Assembly of non-unique insertion content using next-generation sequencing

Por Parrish, Nathaniel, Hormozdiari, Farhad, Eskin, Eleazar
Publicado em 2011

Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions

Por He, Dan, Hormozdiari, Farhad, Furlotte, Nicholas, Eskin, Eleazar
Publicado em 2011

A Spatial Haplotype Copying Model with Applications to Genotype Imputation

Por Yang, Wen-Yun, Hormozdiari, Farhad, Eskin, Eleazar, Pasaniuc, Bogdan
Publicado no J Comput Biol (2015)

Multiple testing correction in linear mixed models

Por Joo, Jong Wha J., Hormozdiari, Farhad, Han, Buhm, Eskin, Eleazar
Publicado no Genome Biol (2016)

Sensitive and fast mapping of di-base encoded reads

Por Hormozdiari, Farhad, Hach, Faraz, Sahinalp, S. Cenk, Eichler, Evan E., Alkan, Can
Publicado em 2011

Sensitive and fast mapping of di-base encoded reads

Por Hormozdiari, Farhad, Hach, Faraz, Sahinalp, S. Cenk, Eichler, Evan E., Alkan, Can
Publicado em 2012

CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping

Por Wang, Zhanyong, Hormozdiari, Farhad, Yang, Wen-Yun, Halperin, Eran, Eskin, Eleazar
Publicado em 2013

Identifying Causal Variants at Loci with Multiple Signals of Association

Por Hormozdiari, Farhad, Kostem, Emrah, Kang, Eun Yong, Pasaniuc, Bogdan, Eskin, Eleazar
Publicado em 2014

Identification of causal genes for complex traits

Por Hormozdiari, Farhad, Kichaev, Gleb, Yang, Wen-Yun, Pasaniuc, Bogdan, Eskin, Eleazar
Publicado no Bioinformatics (2015)

Accelerating read mapping with FastHASH

Por Xin, Hongyi, Lee, Donghyuk, Hormozdiari, Farhad, Yedkar, Samihan, Mutlu, Onur, Alkan, Can
Publicado em 2013

Fast and Accurate Mapping of Complete Genomics Reads

Por Lee, Donghyuk, Hormozdiari, Farhad, Xin, Hongyi, Hach, Faraz, Mutlu, Onur, Alkan, Can
Publicado no Methods (2014)

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data

Por Yang, Wen-Yun, Hormozdiari, Farhad, Wang, Zhanyong, He, Dan, Pasaniuc, Bogdan, Eskin, Eleazar
Publicado em 2013

mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications

Por Hach, Faraz, Sarrafi, Iman, Hormozdiari, Farhad, Alkan, Can, Eichler, Evan E., Sahinalp, S. Cenk
Publicado em 2014

mrsFast: a cache-oblivious algorithm for short-read mapping

Por Hach, Faraz, Hormozdiari, Fereydoun, Alkan, Can, Hormozdiari, Farhad, Birol, Inanc, Eichler, Evan E, Sahinalp, S Cenk
Publicado em 2010

eALPS: Estimating Abundance Levels in Pooled Sequencing Using Available Genotyping Data

Por Eskin, Itamar, Hormozdiari, Farhad, Conde, Lucia, Riby, Jacques, Skibola, Christine F., Eskin, Eleazar, Halperin, Eran
Publicado em 2013

Using genomic annotations increases statistical power to detect eGenes

Por Duong, Dat, Zou, Jennifer, Hormozdiari, Farhad, Sul, Jae Hoon, Ernst, Jason, Han, Buhm, Eskin, Eleazar
Publicado no Bioinformatics (2016)

Privacy preserving protocol for detecting genetic relatives using rare variants

Por Hormozdiari, Farhad, Joo, Jong Wha J, Wadia, Akshay, Guan, Feng, Ostrosky, Rafail, Sahai, Amit, Eskin, Eleazar
Publicado em 2014

PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling

Por Park, Danny S, Baran, Yael, Hormozdiari, Farhad, Eng, Celeste, Torgerson, Dara G, Burchard, Esteban G, Zaitlen, Noah
Publicado no BMC Bioinformatics (2015)

Allele-specific expression and eQTL analysis in mouse adipose tissue

Por Hasin-Brumshtein, Yehudit, Hormozdiari, Farhad, Martin, Lisa, van Nas, Atila, Eskin, Eleazar, Lusis, Aldons J, Drake, Thomas A
Publicado em 2014

Integrating Functional Data to Prioritize Causal Variants in Statistical Fine-Mapping Studies

Por Kichaev, Gleb, Yang, Wen-Yun, Lindstrom, Sara, Hormozdiari, Farhad, Eskin, Eleazar, Price, Alkes L., Kraft, Peter, Pasaniuc, Bogdan
Publicado em 2014