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Full Name
Fereydoun Hormozdiari
Affiliation
University of California davis
ORCID
Career Start Year
2007
Papers
53
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36550274
SVDSS: structural variation discovery in hard-to-call genomic regions using sample-specific strings from accurate long reads.
Nat Methods
2023
35596027
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation.
J Autism Dev Disord
2023
36625266
Dr.Nod: computational framework for discovery of regulatory non-coding drivers in tissue-matched distal regulatory elements.
Nucleic Acids Res
2023
36699383
MAGI-MS: multiple seed-centric module discovery.
Bioinform Adv
2022
33503255
Nebula: ultra-efficient mapping-free structural variant genotyper.
Nucleic Acids Res
2021
36700094
Comparative genome analysis using sample-specific string detection in accurate long reads.
Bioinform Adv
2021
31584621
Meltos: multi-sample tumor phylogeny reconstruction for structural variants.
Bioinformatics
2020
30559488
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Nat Genet
2019
31653223
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
Genome Med
2019
31492842
Functional disease architectures reveal unique biological role of transposable elements.
Nat Commun
2019
31377530
Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants.
iScience
2019
30898144
TAD fusion score: discovery and ranking the contribution of deletions to genome structure.
Genome Biol
2019
30833765
How bioinformatics and open data can boost basic science in countries and universities with limited resources.
Nat Biotechnol
2019
30937433
Discovery of tandem and interspersed segmental duplications using high-throughput sequencing.
Bioinformatics
2019
29618373
Genetic variation associated with increased insecticide resistance in the malaria mosquito, Anopheles coluzzii.
Parasit Vectors
2018
29880660
High-resolution comparative analysis of great ape genomes.
Science
2018
30297454
Combinatorial Approach for Complex Disorder Prediction: Case Study of Neurodevelopmental Disorders.
Genetics
2018
28583483
Toolkit for automated and rapid discovery of structural variants.
Methods
2017
28191889
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Nat Genet
2017
28965761
Genomic Patterns of De Novo Mutation in Simplex Autism.
Cell
2017
26749308
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Am J Hum Genet
2016
27708267
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.
Nat Commun
2016
25378250
The discovery of integrated gene networks for autism and related disorders.
Genome Res
2015
26249230
Global diversity, population stratification, and selection of human copy-number variation.
Science
2015
26432246
An integrated map of structural variation in 2,504 human genomes.
Nature
2015
25883321
Characteristics of de novo structural changes in the human genome.
Genome Res
2015
25383537
Resolving the complexity of the human genome using single-molecule sequencing.
Nature
2015
25116239
Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma.
PLoS One
2014
23721540
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild.
BMC Genomics
2013
23884656
Rates and patterns of great ape retrotransposition.
Proc Natl Acad Sci U S A
2013
23823723
Great ape genetic diversity and population history.
Nature
2013
22294438
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.
J Pathol
2012
22553170
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.
J Pathol
2012
21131385
Alu repeat discovery and characterization within human genomes.
Genome Res
2011
22048523
Simultaneous structural variation discovery among multiple paired-end sequenced genomes.
Genome Res
2011
21625565
deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data.
PLoS Comput Biol
2011
21685127
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee.
Genome Res
2011
21293372
Mapping copy number variation by population-scale genome sequencing.
Nature
2011
21478487
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
Bioinformatics
2011
20078394
Towards improved assessment of functional similarity in large-scale screens: a study on indel length.
J Comput Biol
2010
20500021
Protein-protein interaction network evaluation for identifying potential drug targets.
J Comput Biol
2010
20529927
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.
Bioinformatics
2010
20676076
mrsFAST: a cache-oblivious algorithm for short-read mapping.
Nat Methods
2010
20385726
Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.
Bioinformatics
2010
19213135
Dense graphlet statistics of protein interaction and random networks.
Pac Symp Biocomput
2009
19718026
Personalized copy number and segmental duplication maps using next-generation sequencing.
Nat Genet
2009
19483690
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.
Nat Methods
2009
19447966
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes.
Genome Res
2009
19193143
The effect of insertions and deletions on wirings in protein-protein interaction networks: a large-scale study.
J Comput Biol
2009
18586721
Biomolecular network motif counting and discovery by color coding.
Bioinformatics
2008
1 - 50 of 53
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