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Author Details

Iman Hajirasouliha
Institute for Computational Biomedicine
2008
42
21
PMIDPaper TitleJournal TitlePublished Year
36543475A non-invasive artificial intelligence approach for the prediction of human blastocyst ploidy: a retrospective model development and validation study.Lancet Digit Health2023
37641111Ariadne: synthetic long read deconvolution using assembly graphs.Genome Biol2023
36959322Cue: a deep-learning framework for structural variant discovery and genotyping.Nat Methods2023
35233546System-wide transcriptome damage and tissue identity loss in COVID-19 patients.Cell Rep Med2022
35644123Weakly-supervised tumor purity prediction from frozen H&E stained slides.EBioMedicine2022
34406356coronaSPAdes: from biosynthetic gene clusters to RNA viral assemblies.Bioinformatics2021
33719168A Deep Learning Approach to Diagnostic Classification of Prostate Cancer Using Pathology-Radiology Fusion.J Magn Reson Imaging2021
33712587Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions.Nat Commun2021
33758858Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps.bioRxiv2021
31584621Meltos: multi-sample tumor phylogeny reconstruction for structural variants.Bioinformatics2020
33160516Predictive modeling in reproductive medicine: Where will the future of artificial intelligence research take us?Fertil Steril2020
33160512Precision medicine and artificial intelligence: overview and relevance to reproductive medicine.Fertil Steril2020
33297943gpps: an ILP-based approach for inferring cancer progression with mutation losses from single cell data.BMC Bioinformatics2020
32591764Publisher Correction: Building an international consortium for tracking coronavirus health status.Nat Med2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32511352Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions.bioRxiv2020
32192518VALOR2: characterization of large-scale structural variants using linked-reads.Genome Biol2020
30523036Minerva: an alignment- and reference-free approach to deconvolve Linked-Reads for metagenomics.Genome Res2019
31304368Deep learning enables robust assessment and selection of human blastocysts after in vitro fertilization.NPJ Digit Med2019
31039798The tech for the next decade: promises and challenges in genome biology.Genome Biol2019
31167637BAMSE: Bayesian model selection for tumor phylogeny inference among multiple samples.BMC Bioinformatics2019
31160374BiosyntheticSPAdes: reconstructing biosynthetic gene clusters from assembly graphs.Genome Res2019
29292031Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images.EBioMedicine2018
29927069Using LICHeE and BAMSE for Reconstructing Cancer Phylogenetic Trees.Curr Protoc Bioinformatics2018
25944252Fast and scalable inference of multi-sample cancer lineages.Genome Biol2015
24931984Detecting independent and recurrent copy number aberrations using interval graphs.Bioinformatics2014
25355789Characterization of structural variants with single molecule and hybrid sequencing approaches.Bioinformatics2014
24932008A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data.Bioinformatics2014
24072733MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels.Bioinformatics2013
22399677Mirroring co-evolving trees in the light of their topologies.Bioinformatics2012
22553170From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.J Pathol2012
22294438Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.J Pathol2012
21131385Alu repeat discovery and characterization within human genomes.Genome Res2011
22048523Simultaneous structural variation discovery among multiple paired-end sequenced genomes.Genome Res2011
21293372Mapping copy number variation by population-scale genome sequencing.Nature2011
21478487Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.Bioinformatics2011
20385726Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.Bioinformatics2010
20529927Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.Bioinformatics2010
19415115smyRNA: a novel Ab initio ncRNA gene finder.PLoS One2009
18586721Biomolecular network motif counting and discovery by color coding.Bioinformatics2008
18586730Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies.Bioinformatics2008
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Collaborators

University of California davis
Co-authored papers 11
National Cancer Institute, National Institutes of Health
Co-authored papers 11
Meyer Cancer Center
Co-authored papers 10
Englander Institute for Precision Medicine, The Meyer Cancer Center
Co-authored papers 8
Bilkent University
Co-authored papers 7
Institute for Computational Biomedicine, Weill Cornell Medicine of Cornell University
Co-authored papers 6
Feil Family Brain and Mind Research Institute.
Co-authored papers 6
Columbia University, United States Bureau of Educational and Cultural Affairs Fulbright Program, University of Piraeus, Weill Cornell Medical College, Weill Cornell Medicine
Co-authored papers 6
University of Washington
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New York City College of Technology
Co-authored papers 5
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University of British Columbia
Co-authored papers 5
Columbia Universtiy College of Physicians and Surgeons
Co-authored papers 4
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New York NewYork-Presbyterian Hospital
Co-authored papers 4
Co-authored papers 4
Memorial Sloan Kettering Cancer Center
Co-authored papers 4
Co-authored papers 4
HudsonAlpha Institute for Biotechnology
Co-authored papers 4
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University of California los angeles
Co-authored papers 4
Baylor College of Medicine
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University of Michigan Medical School ann arbor
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Cancer Institute of New Jersey
Co-authored papers 3
Center for Digital Medicine, Heinrich Heine University Dusseldorf
Co-authored papers 3
Google Accelerated Science Team, Google Inc
Co-authored papers 3
Contextual Genomics Inc.
Co-authored papers 3
Ronald O. Perelman and Claudia Cohen Center for Reproductive Medicine
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Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University
Co-authored papers 3
University of Texas MD Anderson Cancer Center
Co-authored papers 3