Spatial metatranscriptomics resolves host–bacteria–fungi interactomes DOI Creative Commons
Sami Saarenpää, Or Shalev, Haim Ashkenazy

et al.

Nature Biotechnology, Journal Year: 2023, Volume and Issue: 42(9), P. 1384 - 1393

Published: Nov. 20, 2023

The interactions of microorganisms among themselves and with their multicellular host take place at the microscale, forming complex networks spatial patterns. Existing technology does not allow simultaneous investigation between a multitude its colonizing microorganisms, which limits our understanding host-microorganism within plant or animal tissue. Here we present metatranscriptomics (SmT), sequencing-based approach that leverages 16S/18S/ITS/poly-d(T) multimodal arrays for transcriptome- microbiome-wide characterization tissues 55-µm resolution. We showcase SmT in outdoor-grown Arabidopsis thaliana leaves as model system, find tissue-scale bacterial fungal hotspots. By network analysis, study inter- intrakingdom well response to microbial provides an answering fundamental questions on host-microbiome interplay.

Language: Английский

Methods and applications for single-cell and spatial multi-omics DOI Open Access
Katy Vandereyken, Alejandro Sifrim, Bernard Thienpont

et al.

Nature Reviews Genetics, Journal Year: 2023, Volume and Issue: 24(8), P. 494 - 515

Published: March 2, 2023

Language: Английский

Citations

606

An introduction to spatial transcriptomics for biomedical research DOI Creative Commons

Cameron G. Williams,

Hyun Jae Lee,

Takahiro Asatsuma

et al.

Genome Medicine, Journal Year: 2022, Volume and Issue: 14(1)

Published: June 27, 2022

Abstract Single-cell transcriptomics (scRNA-seq) has become essential for biomedical research over the past decade, particularly in developmental biology, cancer, immunology, and neuroscience. Most commercially available scRNA-seq protocols require cells to be recovered intact viable from tissue. This precluded many cell types study largely destroys spatial context that could otherwise inform analyses of identity function. An increasing number platforms now facilitate spatially resolved, high-dimensional assessment gene transcription, known as ‘spatial transcriptomics’. Here, we introduce different classes method, which either record locations hybridized mRNA molecules tissue, image positions themselves prior assessment, or employ arrays probes pre-determined location. We review sizes tissue area can assessed, their resolution, genes profiled. discuss if preservation influences choice platform, provide guidance on whether specific may better suited discovery screens hypothesis testing. Finally, bioinformatic methods analysing transcriptomic data, including pre-processing, integration with existing inference cell-cell interactions. Spatial -omics are already improving our understanding human tissues research, diagnostic, therapeutic settings. To build upon these recent advancements, entry-level those seeking own research.

Language: Английский

Citations

462

What is a cell type and how to define it? DOI Creative Commons
Hongkui Zeng

Cell, Journal Year: 2022, Volume and Issue: 185(15), P. 2739 - 2755

Published: July 1, 2022

Language: Английский

Citations

278

Spatially informed cell-type deconvolution for spatial transcriptomics DOI
Ying Ma, Xiang Zhou

Nature Biotechnology, Journal Year: 2022, Volume and Issue: 40(9), P. 1349 - 1359

Published: May 2, 2022

Language: Английский

Citations

277

The emerging landscape of spatial profiling technologies DOI
Jeffrey R. Moffitt, Emma Lundberg, Holger Heyn

et al.

Nature Reviews Genetics, Journal Year: 2022, Volume and Issue: 23(12), P. 741 - 759

Published: July 20, 2022

Language: Английский

Citations

277

hdWGCNA identifies co-expression networks in high-dimensional transcriptomics data DOI Creative Commons
Samuel Morabito, Fairlie Reese, Negin Rahimzadeh

et al.

Cell Reports Methods, Journal Year: 2023, Volume and Issue: 3(6), P. 100498 - 100498

Published: June 1, 2023

Biological systems are immensely complex, organized into a multi-scale hierarchy of functional units based on tightly regulated interactions between distinct molecules, cells, organs, and organisms. While experimental methods enable transcriptome-wide measurements across millions popular bioinformatic tools do not support systems-level analysis. Here we present hdWGCNA, comprehensive framework for analyzing co-expression networks in high-dimensional transcriptomics data such as single-cell spatial RNA sequencing (RNA-seq). hdWGCNA provides functions network inference, gene module identification, enrichment analysis, statistical tests, visualization. Beyond conventional RNA-seq, is capable performing isoform-level analysis using long-read data. We showcase from autism spectrum disorder Alzheimer's disease brain samples, identifying disease-relevant modules. directly compatible with Seurat, widely used R package demonstrate the scalability by dataset containing nearly 1 million cells.

Language: Английский

Citations

267

Spatial profiling technologies illuminate the tumor microenvironment DOI Creative Commons
Ofer Elhanani, Raz Ben-Uri, Leeat Keren

et al.

Cancer Cell, Journal Year: 2023, Volume and Issue: 41(3), P. 404 - 420

Published: Feb. 16, 2023

Language: Английский

Citations

198

Statistical and machine learning methods for spatially resolved transcriptomics data analysis DOI Creative Commons
Zexian Zeng, Yawei Li, Yiming Li

et al.

Genome biology, Journal Year: 2022, Volume and Issue: 23(1)

Published: March 25, 2022

Abstract The recent advancement in spatial transcriptomics technology has enabled multiplexed profiling of cellular transcriptomes and locations. As the capacity efficiency experimental technologies continue to improve, there is an emerging need for development analytical approaches. Furthermore, with continuous evolution sequencing protocols, underlying assumptions current methods be re-evaluated adjusted harness increasing data complexity. To motivate aid future model development, we herein review statistical machine learning transcriptomics, summarize useful resources, highlight challenges opportunities ahead.

Language: Английский

Citations

125

A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics DOI Creative Commons
Haoyang Li, Juexiao Zhou, Zhongxiao Li

et al.

Nature Communications, Journal Year: 2023, Volume and Issue: 14(1)

Published: March 21, 2023

Abstract Spatial transcriptomics technologies are used to profile transcriptomes while preserving spatial information, which enables high-resolution characterization of transcriptional patterns and reconstruction tissue architecture. Due the existence low-resolution spots in recent technologies, uncovering cellular heterogeneity is crucial for disentangling cell types, many related methods have been proposed. Here, we benchmark 18 existing resolving a deconvolution task with 50 real-world simulated datasets by evaluating accuracy, robustness, usability methods. We compare these comprehensively using different metrics, resolutions, spot numbers, gene numbers. In terms performance, CARD, Cell2location, Tangram best conducting task. To refine our comparative results, provide decision-tree-style guidelines recommendations method selection their additional features, will help users easily choose fulfilling concerns.

Language: Английский

Citations

122

RNA velocity unraveled DOI Creative Commons
Gennady Gorin, Meichen Fang, Tara Chari

et al.

PLoS Computational Biology, Journal Year: 2022, Volume and Issue: 18(9), P. e1010492 - e1010492

Published: Sept. 12, 2022

We perform a thorough analysis of RNA velocity methods, with view towards understanding the suitability various assumptions underlying popular implementations. In addition to providing self-contained exposition mathematics, we undertake simulations and controlled experiments on biological datasets assess workflow sensitivity parameter choices biology. Finally, argue for more rigorous approach velocity, present framework Markovian that points directions improvement mitigation current problems.

Language: Английский

Citations

117