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Caleb Hallinan

dblp:426/0787 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2025
0009-0000-9137-1293ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › omics data analysis
batch effect correction
0.912025
Spatial mutual nearest neighbors for spatial transcriptomics data · Bioinform. 2025
Bioinformatics and computational biology
single-cell analysis
0.912025
Spatial mutual nearest neighbors for spatial transcriptomics data · Bioinform. 2025
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatial domain identification
0.912025
Spatial mutual nearest neighbors for spatial transcriptomics data · Bioinform. 2025
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics
0.912025
Spatial mutual nearest neighbors for spatial transcriptomics data · Bioinform. 2025

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

mutual nearest neighbors · 0.9louvain algorithm · 0.9k-nearest neighbor · 0.9
YearPublicationVenuePosition
2025 Spatial mutual nearest neighbors for spatial transcriptomics data
abstract
MOTIVATION: Mutual nearest neighbors (MNN) is a widely used computational tool to perform batch correction for single-cell RNA-sequencing data. However, in applications such as spatial transcriptomics, it fails to take into account the 2D spatial information. RESULTS: Here, we present spatialMNN, an algorithm that integrates multiple spatial transcriptomic samples and identifies spatial domains. Our approach begins by building a k-nearest neighbors (kNN) graph based on the spatial coordinates, prunes noisy edges, and identifies niches to act as anchor points for each sample. Next, we construct a MNN graph across the samples to identify similar niches. Finally, the spatialMNN graph can be partitioned using existing algorithms, such as the Louvain algorithm to predict spatial domains across the tissue samples. We demonstrate the performance of spatialMNN using large datasets, including one with N = 31 10x Genomics Visium samples. We also evaluate the computing performance of spatialMNN to other popular spatial clustering methods. AVAILABILITY AND IMPLEMENTATION: Our software package is available on GitHub (https://github.com/Pixel-Dream/spatialMNN). The code is available on Zenodo (https://doi.org/10.5281/zenodo.15073963).
Haowen Zhou, Pratibha Panwar, Boyi Guo, Caleb Hallinan, Shila Ghazanfar, Stephanie C. Hicks
Bioinform.4