Iman Hajirasouliha

Orcid: 0000-0003-2597-8200

According to our database1, Iman Hajirasouliha authored at least 29 papers between 2007 and 2024.

Collaborative distances:
  • Dijkstra number2 of three.
  • Erdős number3 of two.

Timeline

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Links

On csauthors.net:

Bibliography

2024
Machine learning for structural design models of continuous beam systems via influence zones.
CoRR, 2024

2023
Influence zones for continuous beam systems.
CoRR, 2023

2021
coronaSPAdes: from biosynthetic gene clusters to RNA viral assemblies.
Bioinform., 2021

Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses.
Bioinform., 2021

2020
Reliability of water distribution networks subjected to seismic hazard: Application of an improved entropy function.
Reliab. Eng. Syst. Saf., 2020

gpps: an ILP-based approach for inferring cancer progression with mutation losses from single cell data.
BMC Bioinform., 2020

Meltos: multi-sample tumor phylogeny reconstruction for structural variants.
Bioinform., 2020

2019
Deep learning enables robust assessment and selection of human blastocysts after in vitro fertilization.
npj Digit. Medicine, 2019

BAMSE: Bayesian model selection for tumor phylogeny inference among multiple samples.
BMC Bioinform., 2019

2018
Breast Cancer Histopathological Image Classification: A Deep Learning Approach.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
BAMSE: Bayesian model selection for tumor phylogeny inference among multiple tumor samples.
Proceedings of the 7th IEEE International Conference on Computational Advances in Bio and Medical Sciences, 2017

2014
Fast and Scalable Inference of Multi-Sample Cancer Lineages.
CoRR, 2014

Detecting independent and recurrent copy number aberrations using interval graphs.
Bioinform., 2014

Characterization of structural variants with single molecule and hybrid sequencing approaches.
Bioinform., 2014

A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data.
Bioinform., 2014

Reconstructing Mutational History in Multiply Sampled Tumors Using Perfect Phylogeny Mixtures.
Proceedings of the Algorithms in Bioinformatics - 14th International Workshop, 2014

A combinatorial algorithm to identify independent and recurrent copy number aberrations across cancer types.
Proceedings of the IEEE 4th International Conference on Computational Advances in Bio and Medical Sciences, 2014

2013
MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels.
Bioinform., 2013

2012
Mirroring co-evolving trees in the light of their topologies.
Bioinform., 2012

Convergence to Equilibria in Distributed, Selfish Reallocation Processes with Weighted Tasks.
Algorithmica, 2012

2011
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
Bioinform., 2011

Simultaneous Structural Variation Discovery in Multiple Paired-End Sequenced Genomes.
Proceedings of the Research in Computational Molecular Biology, 2011

2010
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.
Bioinform., 2010

Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.
Bioinform., 2010

A simplified model for seismic response prediction of concentrically braced frames.
Adv. Eng. Softw., 2010

2009
Quantifying Systemic Evolutionary Changes by Color Coding Confidence-Scored PPI Networks.
Proceedings of the Algorithms in Bioinformatics, 9th International Workshop, 2009

2008
Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies.
Proceedings of the Proceedings 16th International Conference on Intelligent Systems for Molecular Biology (ISMB), 2008

Biomolecular network motif counting and discovery by color coding.
Proceedings of the Proceedings 16th International Conference on Intelligent Systems for Molecular Biology (ISMB), 2008

2007
On Completing Latin Squares.
Proceedings of the STACS 2007, 2007


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