Author of the publication

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Using genomic annotations increases statistical power to detect eGenes.

D. Duong, J. Zou, F. Hormozdiari, J. Sul, J. Ernst, B. Han, and E. Eskin. Bioinform., 32 (12): 156-163 (2016)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Farhad Tamadon

Farhad Farahmandi

Farhad Heravi

Farhad Farassat

Farhad Mirghomizadeh

Other publications of authors with the same name

A Spatial-Aware Haplotype Copying Model with Applications to Genotype Imputation.W. Yang, F. Hormozdiari, E. Eskin, and B. Pasaniuc. RECOMB, volume 8394 of Lecture Notes in Computer Science, page 371-384. Springer, (2014)CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping.Z. Wang, F. Hormozdiari, W. Yang, E. Halperin, and E. Eskin. RECOMB, volume 7262 of Lecture Notes in Computer Science, page 326-340. Springer, (2012)Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.Y. Wu, F. Hormozdiari, J. Joo, and E. Eskin. J. Comput. Biol., 26 (11): 1203-1213 (2019)Identifying Causal Variants by Fine Mapping Across Multiple Studies.N. LaPierre, K. Taraszka, H. Huang, R. He, F. Hormozdiari, and E. Eskin. RECOMB, volume 12074 of Lecture Notes in Computer Science, page 257-258. Springer, (2020)Using genomic annotations increases statistical power to detect eGenes.D. Duong, J. Zou, F. Hormozdiari, J. Sul, J. Ernst, B. Han, and E. Eskin. Bioinform., 32 (12): 156-163 (2016)Assembly of non-unique insertion content using next-generation sequencing.N. Parrish, F. Hormozdiari, and E. Eskin. BMC Bioinform., 12 (S-6): S3 (2011)Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.Y. Wu, F. Hormozdiari, J. Joo, and E. Eskin. RECOMB, volume 10229 of Lecture Notes in Computer Science, page 303-317. (2017)Sensitive and fast mapping of di-base encoded reads.F. Hormozdiari, F. Hach, S. Sahinalp, E. Eichler, and C. Alkan. Bioinform., 28 (1): 150 (2012)Accelerating read mapping with FastHASH.H. Xin, D. Lee, F. Hormozdiari, S. Yedkar, O. Mutlu, and C. Alkan. BMC Genom., 14 (S-1): S13 (2013)CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping.Z. Wang, F. Hormozdiari, W. Yang, E. Halperin, and E. Eskin. J. Comput. Biol., 20 (3): 224-236 (2013)

BibSonomy

Disambiguation of "Hormozdiari, Farhad"

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Using genomic annotations increases statistical power to detect eGenes.

Please choose a person to relate this publication to

Farhad Tamadon

Farhad Farahmandi

Farhad Heravi

Farhad Farassat

Farhad Mirghomizadeh

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Hormozdiari, Farhad"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Using genomic annotations increases statistical power to detect eGenes.

Please choose a person to relate this publication to

Farhad Tamadon

Farhad Farahmandi

Farhad Heravi

Farhad Farassat

Farhad Mirghomizadeh

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Using genomic annotations increases statistical power to detect eGenes.