Abstract
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
George I. Gavriilidis, Vasileios Vasileiou, Aspasia Orfanou, Naveed Ishaque
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
europepmc
Confidence 96%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
No local reference links have been materialized yet.
10.1016/j.cels.2021.05.016
10.1016/j.cels.2021.05.016
10.1016/j.cell.2017.10.049
10.1016/j.cell.2017.10.049
DRUG-seq for miniaturized high-throughput transcriptome profiling in drug discovery
10.1038/s41467-018-06500-x · 2018
10.1016/j.cels.2021.05.016
10.1016/j.cels.2021.05.016
Drugmonizome and Drugmonizome-ML: integration and abstraction of small molecule attributes for drug enrichment analysis and machine learning
10.1093/database/baab017 · 2021
Massively parallel CRISPR-based genetic perturbation screening at single-cell resolution
10.1002/advs.202204484 · 2023
10.1016/j.cell.2016.11.038
10.1016/j.cell.2016.11.038
10.1016/j.cell.2016.11.039
10.1016/j.cell.2016.11.039
10.1038/nmeth.4177
10.1038/nmeth.4177
10.1186/s13059-020-02044-w
10.1186/s13059-020-02044-w
10.1038/s41467-020-17440-w
10.1038/s41467-020-17440-w
10.1126/science.aax6234
10.1126/science.aax6234
10.1038/s41592-020-0837-5
10.1038/s41592-020-0837-5
10.1016/j.cell.2020.03.039
10.1016/j.cell.2020.03.039
10.1038/s41592-019-0392-0
10.1038/s41592-019-0392-0
10.1038/s41588-021-00779-1
10.1038/s41588-021-00779-1
10.1016/j.molcel.2017.03.007
10.1016/j.molcel.2017.03.007
10.1038/s41467-021-24324-0
10.1038/s41467-021-24324-0
10.1016/j.cell.2018.11.022
10.1016/j.cell.2018.11.022
High-throughput single-cell chromatin accessibility CRISPR screens enable unbiased identification of regulatory networks in cancer
10.1038/s41467-021-23213-w · 2021
10.1038/s41587-021-00902-x
10.1038/s41587-021-00902-x
10.1038/s41587-021-01160-7
10.1038/s41587-021-01160-7
10.1016/j.molcel.2023.03.013
10.1016/j.molcel.2023.03.013
A dual sgRNA library design to probe genetic modifiers using genome-wide CRISPRi screens
10.1186/s12864-023-09754-y · 2023
Systematic functional interrogation of SARS-CoV-2 host factors using Perturb-seq
10.1038/s41467-023-41788-4 · 2023
scPerturb: harmonized single-cell perturbation data
2024
Model-based understanding of single-cell CRISPR screening
10.1038/s41467-019-10216-x · 2019
scMAGeCK links genotypes with multiple phenotypes in single-cell CRISPR screens
10.1186/s13059-020-1928-4 · 2020
10.1186/s13059-019-1874-1
10.1186/s13059-019-1874-1
SCEPTRE improves calibration and sensitivity in single-cell CRISPR screen analysis
10.1186/s13059-021-02545-2 · 2021
10.1038/s41587-020-0605-1
10.1038/s41587-020-0605-1
10.1101/2023.05.06.539326
10.1101/2023.05.06.539326
ASGARD is a single-cell guided pipeline to aid repurposing of drugs
10.1038/s41467-023-36637-3 · 2023
10.1038/s41587-021-01033-z
10.1038/s41587-021-01033-z
10.1038/s41588-021-00778-2
10.1038/s41588-021-00778-2
10.1038/s41587-020-00803-5
10.1038/s41587-020-00803-5
CellDrift: inferring perturbation responses in temporally sampled single-cell data
10.1093/bib/bbac324 · 2022
ICAT: a novel algorithm to robustly identify cell states following perturbations in single-cell transcriptomes
10.1093/bioinformatics/btad278 · 2023
A unified computational framework for single-cell data integration with optimal transport
10.1038/s41467-022-35094-8 · 2022
10.1038/s41592-023-02040-5
10.1038/s41592-023-02040-5
10.1038/s41573-023-00688-4
10.1038/s41573-023-00688-4 · doi-reference
Three million images and morphological profiles of cells treated with matched chemical and genetic perturbations
10.1038/s41592-024-02241-6 · doi-reference
Explainable multi-task learning for multi-modality biological data analysis
10.1038/s41467-023-37477-x · doi-reference
10.1023/a:1007379606734
10.1023/a:1007379606734 · doi-reference
10.1101/2023.07.17.549216
10.1101/2023.07.17.549216 · doi-reference
10.1101/2023.10.16.561085
10.1101/2023.10.16.561085 · doi-reference
10.1101/2023.05.29.542705
10.1101/2023.05.29.542705 · doi-reference
10.1101/2023.12.07.569910
10.1101/2023.12.07.569910 · doi-reference
scGPT: toward building a foundation model for single-cell multi-omics using generative AI
10.1038/s41592-024-02201-0 · doi-reference
Geneformer: a deep learning model for exploring gene networks
10.1007/s11427-023-2431-x · doi-reference
10.21203/rs.3.rs-3676579/v1
10.21203/rs.3.rs-3676579/v1 · doi-reference
10.1101/2023.07.25.550225
10.1101/2023.07.25.550225 · doi-reference
10.1093/bioinformatics/btad387
10.1093/bioinformatics/btad387 · doi-reference
10.1101/2022.07.20.500854
10.1101/2022.07.20.500854 · doi-reference
10.1038/s41467-021-23518-w
10.1038/s41467-021-23518-w · doi-reference
Biologically informed deep learning to query gene programs in single-cell atlases
10.1038/s41556-022-01072-x · doi-reference
10.1016/j.patter.2023.100817
10.1016/j.patter.2023.100817 · doi-reference
VEGA is an interpretable generative model for inferring biological network activity in single-cell transcriptomics
10.1038/s41467-021-26017-0 · doi-reference
Predicting cellular responses to complex perturbations in high‐throughput screens.
10.15252/msb.202211517 · doi-reference
10.1093/bioinformatics/btaa800
10.1093/bioinformatics/btaa800 · doi-reference
10.1038/s41592-019-0494-8
10.1038/s41592-019-0494-8 · doi-reference
Gene knockout inference with variational graph autoencoder learning single-cell gene regulatory networks
10.1093/nar/gkad450 · doi-reference
SCING: Inference of robust, interpretable gene regulatory networks from single cell and spatial transcriptomics
10.1016/j.isci.2023.107124 · doi-reference
10.1038/nmeth.4463
10.1038/nmeth.4463 · doi-reference
10.1038/s41592-023-01938-4
10.1038/s41592-023-01938-4 · doi-reference
RENGE infers gene regulatory networks using time-series single-cell RNA-seq data with CRISPR perturbations
10.1038/s42003-023-05594-4 · doi-reference
10.1101/2023.04.19.537364
10.1101/2023.04.19.537364 · doi-reference
10.1016/j.stemcr.2022.11.010
10.1016/j.stemcr.2022.11.010 · doi-reference
10.1038/s41586-022-05688-9
10.1038/s41586-022-05688-9 · doi-reference
NetBID2 provides comprehensive hidden driver analysis
10.1038/s41467-023-38335-6 · doi-reference
10.1038/s41592-023-02144-y
10.1038/s41592-023-02144-y · doi-reference
Predicting heterogeneity in clone-specific therapeutic vulnerabilities using single-cell transcriptomic signatures
10.1186/s13073-021-01000-y · doi-reference