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Author Details
Full Name
Iman Hajirasouliha
Affiliation
Institute for Computational Biomedicine
ORCID
Career Start Year
2008
Papers
42
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36543475
A non-invasive artificial intelligence approach for the prediction of human blastocyst ploidy: a retrospective model development and validation study.
Lancet Digit Health
2023
37641111
Ariadne: synthetic long read deconvolution using assembly graphs.
Genome Biol
2023
36959322
Cue: a deep-learning framework for structural variant discovery and genotyping.
Nat Methods
2023
35233546
System-wide transcriptome damage and tissue identity loss in COVID-19 patients.
Cell Rep Med
2022
35644123
Weakly-supervised tumor purity prediction from frozen H&E stained slides.
EBioMedicine
2022
34406356
coronaSPAdes: from biosynthetic gene clusters to RNA viral assemblies.
Bioinformatics
2021
33719168
A Deep Learning Approach to Diagnostic Classification of Prostate Cancer Using Pathology-Radiology Fusion.
J Magn Reson Imaging
2021
33712587
Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions.
Nat Commun
2021
33758858
Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps.
bioRxiv
2021
31584621
Meltos: multi-sample tumor phylogeny reconstruction for structural variants.
Bioinformatics
2020
33160516
Predictive modeling in reproductive medicine: Where will the future of artificial intelligence research take us?
Fertil Steril
2020
33160512
Precision medicine and artificial intelligence: overview and relevance to reproductive medicine.
Fertil Steril
2020
33297943
gpps: an ILP-based approach for inferring cancer progression with mutation losses from single cell data.
BMC Bioinformatics
2020
32591764
Publisher Correction: Building an international consortium for tracking coronavirus health status.
Nat Med
2020
32699374
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
32541955
A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
32511352
Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions.
bioRxiv
2020
32192518
VALOR2: characterization of large-scale structural variants using linked-reads.
Genome Biol
2020
30523036
Minerva: an alignment- and reference-free approach to deconvolve Linked-Reads for metagenomics.
Genome Res
2019
31304368
Deep learning enables robust assessment and selection of human blastocysts after in vitro fertilization.
NPJ Digit Med
2019
31039798
The tech for the next decade: promises and challenges in genome biology.
Genome Biol
2019
31167637
BAMSE: Bayesian model selection for tumor phylogeny inference among multiple samples.
BMC Bioinformatics
2019
31160374
BiosyntheticSPAdes: reconstructing biosynthetic gene clusters from assembly graphs.
Genome Res
2019
29292031
Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images.
EBioMedicine
2018
29927069
Using LICHeE and BAMSE for Reconstructing Cancer Phylogenetic Trees.
Curr Protoc Bioinformatics
2018
25944252
Fast and scalable inference of multi-sample cancer lineages.
Genome Biol
2015
24931984
Detecting independent and recurrent copy number aberrations using interval graphs.
Bioinformatics
2014
25355789
Characterization of structural variants with single molecule and hybrid sequencing approaches.
Bioinformatics
2014
24932008
A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data.
Bioinformatics
2014
24072733
MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels.
Bioinformatics
2013
22399677
Mirroring co-evolving trees in the light of their topologies.
Bioinformatics
2012
22553170
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.
J Pathol
2012
22294438
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive 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
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
20385726
Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.
Bioinformatics
2010
20529927
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.
Bioinformatics
2010
19415115
smyRNA: a novel Ab initio ncRNA gene finder.
PLoS One
2009
18586721
Biomolecular network motif counting and discovery by color coding.
Bioinformatics
2008
18586730
Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies.
Bioinformatics
2008
1 - 42 of 42
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