Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.06.08.727881

MipSScs: Artificial neural network-based data integration of 2D/3D single-cell spatial RNA sequence data from virus-infected human cerebral organoids

Abstract

There is interest in the use of recent single-cell spatial transcriptomic technologies to gain biological insights into disease mechanisms. Previously, we characterized the use of herpes simplex virus 1 (HSV-1) induced neuroinflammation in 2D dissociated cells from human cerebral organoids (dcOrgs) to model molecular and transcriptomic readouts associated with Alzheimers disease (AD). In this work, we generated two datasets by using single-cell non-spatial RNA sequencing and single-cell spatial RNA sequencing technologies on HSV-1-infected 2D dcOrgs and HSV-1-infected 3D cerebral organoids (cOrgs). We conducted cell type assignment for the cells in the 2D dcOrgs and 3D cOrgs, by using single-cell non-spatial RNA sequence data from human fetal brains and adult post-mortem brains, to infer the transcriptomic effects of AD-associated in-vitro perturbations through viral infections linked to AD. We evaluated computational and machine learning methods, including the use of multi-layer perceptrons (MLPs), and we used cross-2D/3D platform comparisons as a benchmark to evaluate the artificial neural network models. In the process, we found that the use of MLPs can lead to high validation rates for assigning cell type identities from 2D and 3D human cerebral organoids to cell types found in human adult post-mortem brain samples. Furthermore, the use of these technologies and systems enabled the identification of pseudotime trajectories and cell clusters associated with the viral transcriptional life cycle. We identified several cell types, including endothelial cells and astrocytes, with significantly more clustered cell-cell nearest neighbor distances in infected 3D cOrgs compared to mock 3D cOrgs. Permutation tests revealed that these differences in nearest neighbor distances are unlikely to be driven by overall structural differences between individual infected 3D cOrgs and mock 3D cOrgs, such as differences in the density of cells. Given that there are more large-scale single-cell non-spatial (2D) RNA sequence datasets that had been generated from human post-mortem brain samples, compared to single-cell spatial (3D) RNA sequence datasets from human post-mortem brain samples, the development of data integration approaches by using artificial neural networks such as MLPs, across 2D and 3D single-cell transcriptomics datasets generated from human post-mortem brain samples and human in-vitro systems such as brain organoids is likely to be critical to gain novel insights into neurodegenerative diseases such as AD.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Doddi, A. D., Dawes, P., Chan, Y., Lim, E. T.. 2026-06-11. MipSScs: Artificial neural network-based data integration of 2D/3D single-cell spatial RNA sequence data from virus-infected human cerebral organoids. https://doi.org/10.64898/2026.06.08.727881

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Genome-wide diversity across 130 years reveals drastic post-bottleneck genetic erosion in a recovering population of golden eagles (Aquila chrysaetos)

Many wild populations have experienced severe human-induced declines, but the genetic consequences of such bottlenecks are often poorly understood. In Finland, as well as in many other countries, golden eagles were heavily persecuted during the 19th-20th centuries, disappearing from southern regions and reaching their lowest population size in the 1950-1960s. Although conservation efforts facilitated demographic recovery, the long-term genomic consequences of the bottleneck remained unknown. Here, we used whole-genome sequencing data spanning 136 years to evaluate patterns of genetic diversity in 26 Finnish golden eagles before, during, and after the mid-20th century bottleneck. We found substantial loss of genetic variation, including an 82% reduction in genome-wide heterozygosity, a 42% decline in nucleotide diversity, a 67% reduction in Watterson's theta, and a substantial loss of variable sites. Analyses of the site frequency spectrum and Tajima's D confirmed historical population contraction, and runs of homozygosity analysis indicated elevated post-bottleneck inbreeding. These results indicate strong genetic erosion in Finnish golden eagles despite the census size recovery. Therefore, incorporating genomic indicators in conservation monitoring and performing regional assessments are necessary to guide management and preserve biodiversity in line with the Global Biodiversity Framework's goal of maintaining genetic variation.

genomics↗

Long-read analysis of complete human 5S rDNA arrays reveals a zoned organization with two-state unit methylation linked to chromatin architecture

Despite the fundamental importance of the 5S ribosomal DNA (rDNA) to all cellular life, the landscape of its units by position along its array has remained poorly understood. Here, recent telomere-to-telomere long-read sequencing is used to resolve 5S rDNA arrays from flank to flank and to follow the state of each unit along single molecules. The array is zoned at both the sequence and the epigenetic level. Notably, methylation is bimodal at the level of the unit, and the combination of low-methylation and high-methylation units gives rise to the overall methylation pattern of the array. Moreover, the average number of low-methylation units remains relatively constant regardless of array length. Chromatin fiber sequencing (Fiber-seq) data further show that low-methylation units are more accessible, have lower nucleosome occupancy and are more frequently footprinted at the TFIIIB-binding site, consistent with analyses of ATAC-seq and ChIP-seq data from cell lines. Across species, this pattern is shared among apes, whereas other species show diverse patterns. These results provide a unit-resolved view of the human 5S rDNA array and reveal a zone-specific organization of unit methylation that is associated with chromatin architecture.

genomics↗

Using Oyster Genomics to Understand Human Health

As sessile filter feeders that experience continuous environmental exposure, oysters, particularly Crassostrea virginica, offer a unique opportunity to understand how environmental exposure alters the genome and influence health. Furthermore, oysters must be sorted by size for market value for premium size and taste. However, it requires intensive labor, specialized equipment (tumblers), and is susceptible to environmental risks like pollution. Therefore, it is desirable to produce uniform oysters without machines. However, limitations in the previous reference genome [2] have constrained our understanding of how genes are organized and maintained in oyster populations. To this end, we harvested 240 adult oysters in same location, 120 extremely large size and 120 extremely small, controlled with all confounding factors such as age and water temperature. We perform a genome wise associate study (GWAS) using next generation whole genome sequencing, aiming to discover genomic regions associated with oyster size. Using PacBio HiFi, Illumina, and Hi-C technologies, we generated a 99.7% complete chromosome-level genome assembly for C. virginica (NCBI RefSeq GCF_053477285.1) [75]. We identified a ~13 Mb region on chromosome 1 uniquely expanded in C. virginica and enriched for innate immune and stress-response genes. To evaluate whether these structural features are reflected at the population level, we then conducted a k-mer analysis. This revealed differential sequence patterns by size, including enrichment of bacterial DNA in smaller individuals and host variation at the RNF213 locus within this region. By highlighting genome structure as a mediator of immune resilience, this work supports the use of oysters as sentinels to advance out understanding of how the dynamic reassembly of the genome due to environmental exposures influence health in human populations.

genomics↗