Liran Juan

Orcid: 0000-0001-8826-0269

According to our database1, Liran Juan authored at least 18 papers between 2009 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2023
An interpretable single-cell RNA sequencing data clustering method based on latent Dirichlet allocation.
Briefings Bioinform., July, 2023

2022
A Neighborhood-Based Global Network Model to Predict Drug-Target Interactions.
IEEE ACM Trans. Comput. Biol. Bioinform., 2022

2021
SC2disease: a manually curated database of single-cell transcriptome for human diseases.
Nucleic Acids Res., 2021

2020
ERDS-Exome: A Hybrid Approach for Copy Number Variant Detection from Whole-Exome Sequencing Data.
IEEE ACM Trans. Comput. Biol. Bioinform., 2020

Evaluating individual genome similarity with a topic model.
Bioinform., 2020

FunEffector-Pred: Identification of Fungi Effector by Activate Learning and Genetic Algorithm Sampling of Imbalanced Data.
IEEE Access, 2020

NCRR: A novel method for measuring disease similarity based on non-coding RNA regulation.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020

Assessment of Machine Learning Methods for Classification in Single Cell ATAC-seq.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020

2019
LncDisAP: a computation model for LncRNA-disease association prediction based on multiple biological datasets.
BMC Bioinform., 2019

Prioritizing candidate diseases-related metabolites based on literature and functional similarity.
BMC Bioinform., 2019

2018
Predicting candidate disease-related lncRNAs based on network random walk.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

Identifying Candidate Diseases-related Metabolites Based on Disease Similarity.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
FNSemSim: An improved disease similarity method based on network fusion.
Proceedings of the 2017 IEEE International Conference on Bioinformatics and Biomedicine, 2017

2016
Joint detection of copy number variations in parent-offspring trios.
Bioinform., 2016

2015
Family genome browser: visualizing genomes with pedigree information.
Bioinform., 2015

2014
The personal genome browser: visualizing functions of genetic variants.
Nucleic Acids Res., 2014

2010
Prioritization of disease microRNAs through a human phenome-microRNAome network.
BMC Syst. Biol., 2010

2009
miR2Disease: a manually curated database for microRNA deregulation in human disease.
Nucleic Acids Res., 2009


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