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Genome Biology
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March 23, 2019
TAD fusion score: discovery and ranking the contribution of deletions to genome structure
Linh Huynh, Fereydoun Hormozdiari
Nucleic Acids Research
|
January 27, 2021
Nebula: ultra-efficient mapping-free structural variant genotyper
Parsoa Khorsand, Fereydoun Hormozdiari
Genetics
|
October 10, 2018
Combinatorial Approach for Complex Disorder Prediction: Case Study of Neurodevelopmental Disorders
Linh Huynh, Fereydoun Hormozdiari
Journal of Autism and Developmental Disorders
|
May 20, 2022
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation
Julie C Chow, Fereydoun Hormozdiari
Bioinformatics Advances
|
January 26, 2023
MAGI-MS: multiple seed-centric module discovery
Julie C Chow, Ryan Zhou, Fereydoun Hormozdiari
Methods (San Diego, Calif.)
|
June 7, 2017
Toolkit for automated and rapid discovery of structural variants
Arda Soylev, Can Kockan, Fereydoun Hormozdiari, et al.
Iscience
|
August 5, 2019
Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants
Daniel S Standage, C Titus Brown, Fereydoun Hormozdiari
Nature Methods
|
June 2, 2009
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions
Seunghak Lee, Fereydoun Hormozdiari, Can Alkan, et al.
Bioinformatics (Oxford, England)
|
July 1, 2008
Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies
Iman Hajirasouliha, Fereydoun Hormozdiari, S Cenk Sahinalp, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology
|
May 27, 2010
Protein-protein interaction network evaluation for identifying potential drug targets
Fereydoun Hormozdiari, Raheleh Salari, Vineet Bafna, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 54) with videos related to
Sort By:
Page
of 6
Genome Biology
|
March 23, 2019
TAD fusion score: discovery and ranking the contribution of deletions to genome structure
Linh Huynh, Fereydoun Hormozdiari
Nucleic Acids Research
|
January 27, 2021
Nebula: ultra-efficient mapping-free structural variant genotyper
Parsoa Khorsand, Fereydoun Hormozdiari
Genetics
|
October 10, 2018
Combinatorial Approach for Complex Disorder Prediction: Case Study of Neurodevelopmental Disorders
Linh Huynh, Fereydoun Hormozdiari
Journal of Autism and Developmental Disorders
|
May 20, 2022
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation
Julie C Chow, Fereydoun Hormozdiari
Bioinformatics Advances
|
January 26, 2023
MAGI-MS: multiple seed-centric module discovery
Julie C Chow, Ryan Zhou, Fereydoun Hormozdiari
Methods (San Diego, Calif.)
|
June 7, 2017
Toolkit for automated and rapid discovery of structural variants
Arda Soylev, Can Kockan, Fereydoun Hormozdiari, et al.
Iscience
|
August 5, 2019
Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants
Daniel S Standage, C Titus Brown, Fereydoun Hormozdiari
Nature Methods
|
June 2, 2009
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions
Seunghak Lee, Fereydoun Hormozdiari, Can Alkan, et al.
Bioinformatics (Oxford, England)
|
July 1, 2008
Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies
Iman Hajirasouliha, Fereydoun Hormozdiari, S Cenk Sahinalp, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology
|
May 27, 2010
Protein-protein interaction network evaluation for identifying potential drug targets
Fereydoun Hormozdiari, Raheleh Salari, Vineet Bafna, et al.
Page
of 6