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Nicholas Robertson

dblp:370/5673 · DBLP profile ↗
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2ranked-venue papers
0as first author
2since 2021 · last 2025
—ORCID · conflict

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 93% Computational science and engineering · 7%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
cell-cell interaction analysis
0.912025
SpatioMark: quantifying the impact of spatial proximity on cell phenotype · Bioinform. 2025
Bioinformatics and computational biology › omics data analysis
spatial omics
0.912025
SpatioMark: quantifying the impact of spatial proximity on cell phenotype · Bioinform. 2025
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics
0.712023
MoleculeExperiment enables consistent infrastructure for molecule-resolved spatial omics data in bioconductor · Bioinform. 2023
Computational science and engineering
data infrastructure
0.212023
MoleculeExperiment enables consistent infrastructure for molecule-resolved spatial omics data in bioconductor · Bioinform. 2023
Bioinformatics and computational biology › single-cell analysis
single-cell transcriptomics
0.212023
MoleculeExperiment enables consistent infrastructure for molecule-resolved spatial omics data in bioconductor · Bioinform. 2023

Methods — techniques the papers use, named apart from their topics

statistical framework · 0.9r/bioconductor package · 0.7
YearPublicationVenuePosition
2025 SpatioMark: quantifying the impact of spatial proximity on cell phenotype
abstract
MOTIVATION: As research advances in spatially resolving the biological archetype of various diseases, technologies that capture the spatial relationships between cells are demonstrating increasing value. Whilst there are an increasing number of analytical methods being developed to identify the complex web of interactions between cells, the downstream impacts of these cell-cell relationships are under explored. RESULTS: We present SpatioMark, a statistical framework that simplifies the assessment of gene or protein expression changes within a cell type that are associated with the spatial proximity to other cell types. We demonstrate its performance across spatial proteomics and transcriptomics datasets. We link identified relationships with differences in patient survival. We highlight key challenges in identifying changes in molecular markers associated with the localization of cells. We propose correction strategies that reduce artefact-induced relationships. AVAILABILITY AND IMPLEMENTATION: SpatioMark is implemented in the Statial R package on Bioconductor: https://bioconductor.org/packages/release/bioc/html/Statial.html.
Sourish S. Iyengar, Alex R. Qin, Nicholas Robertson, Andrew N. Harman, Ellis Patrick
Bioinform.3
2023 MoleculeExperiment enables consistent infrastructure for molecule-resolved spatial omics data in bioconductor
abstract
MOTIVATION: Imaging-based spatial transcriptomics (ST) technologies have achieved subcellular resolution, enabling detection of individual molecules in their native tissue context. Data associated with these technologies promise unprecedented opportunity toward understanding cellular and subcellular biology. However, in R/Bioconductor, there is a scarcity of existing computational infrastructure to represent such data, and particularly to summarize and transform it for existing widely adopted computational tools in single-cell transcriptomics analysis, including SingleCellExperiment and SpatialExperiment (SPE) classes. With the emergence of several commercial offerings of imaging-based ST, there is a pressing need to develop consistent data structure standards for these technologies at the individual molecule-level. RESULTS: To this end, we have developed MoleculeExperiment, an R/Bioconductor package, which (i) stores molecule and cell segmentation boundary information at the molecule-level, (ii) standardizes this molecule-level information across different imaging-based ST technologies, including 10× Genomics' Xenium, and (iii) streamlines transition from a MoleculeExperiment object to a SpatialExperiment object. Overall, MoleculeExperiment is generally applicable as a data infrastructure class for consistent analysis of molecule-resolved spatial omics data. AVAILABILITY AND IMPLEMENTATION: The MoleculeExperiment package is publicly available on Bioconductor at https://bioconductor.org/packages/release/bioc/html/MoleculeExperiment.html. Source code is available on Github at: https://github.com/SydneyBioX/MoleculeExperiment. The vignette for MoleculeExperiment can be found at https://bioconductor.org/packages/release/bioc/html/MoleculeExperiment.html.
Bárbara Zita Peters Couto, Nicholas Robertson, Ellis Patrick, Shila Ghazanfar
Bioinform.2