Probabilistic cell/domain-type assignment of spatial transcriptomics data with SpatialAnno

Author:

Shi Xingjie1,Yang Yi2,Ma Xiaohui3,Zhou Yong1,Guo Zhenxing4,Wang Chaolong5ORCID,Liu Jin4ORCID

Affiliation:

1. KLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University , Shanghai 200062, China

2. The Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University , Nanjing 210018, China

3. College of Life Sciences, Nanjing University , Nanjing 210033, China

4. School of Data Science, The Chinese University of Hong Kong-Shenzhen , Shenzhen 518172, China

5. Department of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430070, China

Abstract

Abstract In the analysis of both single-cell RNA sequencing (scRNA-seq) and spatially resolved transcriptomics (SRT) data, classifying cells/spots into cell/domain types is an essential analytic step for many secondary analyses. Most of the existing annotation methods have been developed for scRNA-seq datasets without any consideration of spatial information. Here, we present SpatialAnno, an efficient and accurate annotation method for spatial transcriptomics datasets, with the capability to effectively leverage a large number of non-marker genes as well as ‘qualitative’ information about marker genes without using a reference dataset. Uniquely, SpatialAnno estimates low-dimensional embeddings for a large number of non-marker genes via a factor model while promoting spatial smoothness among neighboring spots via a Potts model. Using both simulated and four real spatial transcriptomics datasets from the 10x Visium, ST, Slide-seqV1/2, and seqFISH platforms, we showcase the method’s improved spatial annotation accuracy, including its robustness to the inclusion of marker genes for irrelevant cell/domain types and to various degrees of marker gene misspecification. SpatialAnno is computationally scalable and applicable to SRT datasets from different platforms. Furthermore, the estimated embeddings for cellular biological effects facilitate many downstream analyses.

Funder

National Key R&D Program of China

University Development Fund from The Chinese University of Hong Kong, Shenzhen

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Oxford University Press (OUP)

Subject

Genetics

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